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Tytuł:
An immunogenetic basis for lung cancer risk.
Autorzy:
Krishna C; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Tervi A; Institute for Molecular Medicine, Finland (FIMM), HiLIFE, University of Helsinki, Helsinki 00290, Finland.
Saffern M; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Wilson EA; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Yoo SK; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Mars N; Institute for Molecular Medicine, Finland (FIMM), HiLIFE, University of Helsinki, Helsinki 00290, Finland.
Roudko V; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Cho BA; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Jones SE; Institute for Molecular Medicine, Finland (FIMM), HiLIFE, University of Helsinki, Helsinki 00290, Finland.
Vaninov N; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Selvan ME; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Gümüş ZH; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Center for Thoracic Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Lenz TL; Research Unit for Evolutionary Immunogenomics, Department of Biology, Universität Hamburg, 20146 Hamburg, Germany.
Merad M; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Human Immune Monitoring Center, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Boffetta P; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, 40138 Bologna, Italy.; Stony Brook Cancer Center, Stony Brook University, New York, NY 11794, USA.
Martínez-Jiménez F; Vall d'Hebron Institute of Oncology, Barcelona 08035, Spain.; Hartwig Medical Foundation, Amsterdam 1098 XH, the Netherlands.
Ollila HM; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Institute for Molecular Medicine, Finland (FIMM), HiLIFE, University of Helsinki, Helsinki 00290, Finland.; Center for Genomic Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.; Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
Samstein RM; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Center for Thoracic Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Radiation Oncology, Mount Sinai Hospital, New York, NY 10029, USA.
Chowell D; The Marc and Jennifer Lipschultz Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Immunology and Immunotherapy, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Icahn Genomics Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.; Department of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
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Corporate Authors:
FinnGen§
Źródło:
Science (New York, N.Y.) [Science] 2024 Feb 23; Vol. 383 (6685), pp. eadi3808. Date of Electronic Publication: 2024 Feb 23.
Typ publikacji:
Journal Article
MeSH Terms:
Histocompatibility Antigens Class II*/genetics
Lung Neoplasms*/genetics
Lung Neoplasms*/immunology
Loss of Heterozygosity*
Immunologic Surveillance*/genetics
Genetic Predisposition to Disease*
Humans ; Macrophages, Alveolar/immunology ; Risk Factors ; Smoking/immunology ; Middle Aged ; Aged ; Aged, 80 and over ; Chromosome Mapping ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Loss of Heterozygosity and Its Importance in Evolution.
Autorzy:
Smukowski Heil C; Department of Biological Sciences, North Carolina State University, Raleigh, NC, USA. .
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Źródło:
Journal of molecular evolution [J Mol Evol] 2023 Jun; Vol. 91 (3), pp. 369-377. Date of Electronic Publication: 2023 Feb 08.
Typ publikacji:
Journal Article; Review; Research Support, N.I.H., Extramural
MeSH Terms:
Saccharomyces cerevisiae*/genetics
Loss of Heterozygosity*/genetics
Mutation/genetics ; Mutation Rate ; Genome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved.
Autorzy:
Risinskaya N; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Gladysheva M; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Abdulpatakhov A; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Chabaeva Y; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Surimova V; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Aleshina O; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Yushkova A; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Dubova O; National Medical Research Center for Hematology, 125167 Moscow, Russia.; Institute of Biodesign and Modeling of Complex Systems, I.M. Sechenov First Moscow State Medical University, 119991 Moscow, Russia.
Kapranov N; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Galtseva I; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Kulikov S; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Obukhova T; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Sudarikov A; National Medical Research Center for Hematology, 125167 Moscow, Russia.
Parovichnikova E; National Medical Research Center for Hematology, 125167 Moscow, Russia.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Dec 18; Vol. 24 (24). Date of Electronic Publication: 2023 Dec 18.
Typ publikacji:
Journal Article
MeSH Terms:
Precursor Cell Lymphoblastic Leukemia-Lymphoma*/genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma*/pathology
Immediate-Early Proteins*/genetics
Adult ; Humans ; DNA Copy Number Variations ; Chromosome Aberrations ; DNA ; Loss of Heterozygosity ; Nuclear Proteins/genetics ; Tumor Suppressor Proteins/genetics ; Guanine Nucleotide Exchange Factors/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Evolution of loss of heterozygosity patterns in hybrid genomes of Candida yeast pathogens.
Autorzy:
Mixão V; Life Sciences Department, Barcelona Supercomputing Center (BSC), Jordi Girona, 29, 08034, Barcelona, Spain.; Mechanisms of Disease Program, Institute for Research in Biomedicine (IRB), The Barcelona Institute of Science and Technology, Barcelona, Spain.; Present address: Genomics and Bioinformatics Unit, Infectious Diseases Department, National Institute of Health Dr. Ricardo Jorge, Av. Padre Cruz, 1649-016, Lisbon, Portugal.
Nunez-Rodriguez JC; Life Sciences Department, Barcelona Supercomputing Center (BSC), Jordi Girona, 29, 08034, Barcelona, Spain.; Mechanisms of Disease Program, Institute for Research in Biomedicine (IRB), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Del Olmo V; Life Sciences Department, Barcelona Supercomputing Center (BSC), Jordi Girona, 29, 08034, Barcelona, Spain.; Mechanisms of Disease Program, Institute for Research in Biomedicine (IRB), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Ksiezopolska E; Life Sciences Department, Barcelona Supercomputing Center (BSC), Jordi Girona, 29, 08034, Barcelona, Spain.; Mechanisms of Disease Program, Institute for Research in Biomedicine (IRB), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Saus E; Life Sciences Department, Barcelona Supercomputing Center (BSC), Jordi Girona, 29, 08034, Barcelona, Spain.; Mechanisms of Disease Program, Institute for Research in Biomedicine (IRB), The Barcelona Institute of Science and Technology, Barcelona, Spain.
Boekhout T; Westerdijk Fungal Biodiversity Institute, Utrecht, The Netherlands.; Institute of Biodiversity and Ecosystem Dynamics (IBED), University of Amsterdam, Amsterdam, The Netherlands.
Gacser A; Department of Microbiology, University of Szeged, Szeged, Hungary.; MTA-SZTE 'Lendület' Mycobiome Research Group, University of Szeged, Szeged, Hungary.
Gabaldón T; Life Sciences Department, Barcelona Supercomputing Center (BSC), Jordi Girona, 29, 08034, Barcelona, Spain. .; Mechanisms of Disease Program, Institute for Research in Biomedicine (IRB), The Barcelona Institute of Science and Technology, Barcelona, Spain. .; ICREA, Pg. Lluis Companys 23, 08010, Barcelona, Spain. .; Centro de Investigación Biomédica En Red de Enfermedades Infecciosas, Barcelona, Spain. .
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Źródło:
BMC biology [BMC Biol] 2023 May 11; Vol. 21 (1), pp. 105. Date of Electronic Publication: 2023 May 11.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Candida*/genetics
Genome*
Loss of Heterozygosity ; Chromosomes ; Phenotype
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Characterization and clinical evaluation of microsatellite instability and loss of heterozygosity within tumor-related genes in colorectal cancer.
Autorzy:
Huo X; School of Basic Medical Sciences, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research, Beijing, 100069, China.
Feng D; School of Basic Medical Sciences, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research, Beijing, 100069, China.
Zhang S; Institute of Laboratory Animal Sciences, Chinese Academy of Medical Sciences and Comparative Medicine Center, Peking Union Medical Collage, Beijing, 100021 , China.
Li Z; School of Basic Medical Sciences, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research, Beijing, 100069, China.
Li X; School of Basic Medical Sciences, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research, Beijing, 100069, China.
Li C; School of Basic Medical Sciences, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research, Beijing, 100069, China.
Guo M; School of Basic Medical Sciences, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research, Beijing, 100069, China.
Wang J; Department of General Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research & National Clinical Research Center for Digestive Diseases, Beijing, 100050, China.
Zhang Z; Department of General Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research & National Clinical Research Center for Digestive Diseases, Beijing, 100050, China.
Lu Q; Department of Ophthalmology and Visual Sciences, University of Louisville School of Medicine, Louisville, KY, 40202, USA.
Du X; School of Basic Medical Sciences, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research, Beijing, 100069, China.
Bai Z; Department of General Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research & National Clinical Research Center for Digestive Diseases, Beijing, 100050, China. bai_.
Chen Z; School of Basic Medical Sciences, Capital Medical University, Beijing Key Laboratory of Cancer Invasion & Metastasis Research, Beijing, 100069, China. .
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Źródło:
BMC medical genomics [BMC Med Genomics] 2021 Sep 25; Vol. 14 (1), pp. 235. Date of Electronic Publication: 2021 Sep 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Loss of Heterozygosity*
Microsatellite Instability*
Biomarkers, Tumor/*genetics
Colorectal Neoplasms/*genetics
Aged ; Aged, 80 and over ; Antineoplastic Agents/therapeutic use ; Cohort Studies ; Colorectal Neoplasms/drug therapy ; Colorectal Neoplasms/pathology ; Female ; Humans ; Male ; Middle Aged ; Neoplasm Staging ; Prognosis ; Survival Analysis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Pan-cancer analysis of whole-genome doubling and its association with patient prognosis.
Autorzy:
Kikutake C; Medical Institute of Bioregulation, Kyushu University, Fukuoka, 812-8582, Japan.
Suyama M; Medical Institute of Bioregulation, Kyushu University, Fukuoka, 812-8582, Japan. .
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Źródło:
BMC cancer [BMC Cancer] 2023 Jul 03; Vol. 23 (1), pp. 619. Date of Electronic Publication: 2023 Jul 03.
Typ publikacji:
Journal Article
MeSH Terms:
Genome, Human*
Neoplasms*/genetics
Humans ; Mutation ; Loss of Heterozygosity ; Prognosis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Comprehensive Genetic Study of Malignant Cervical Paraganglioma.
Autorzy:
Snezhkina A; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Pavlov V; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Fedorova M; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Kalinin D; Vishnevsky Institute of Surgery, Ministry of Health of the Russian Federation, 117997 Moscow, Russia.
Pudova E; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Kobelyatskaya A; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Bakhtogarimov I; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Krasnov G; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Kudryavtseva A; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 May 04; Vol. 24 (9). Date of Electronic Publication: 2023 May 04.
Typ publikacji:
Case Reports
MeSH Terms:
Paraganglioma*/genetics
Paraganglioma*/pathology
Humans ; Mutation ; Germ-Line Mutation ; Loss of Heterozygosity
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Human chromosome 3p21.3 carries TERT transcriptional regulators in pancreatic cancer.
Autorzy:
Yagyu T; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.; Department of Molecular and Cellular Biology, Division of Genome and Cellular Function, Tottori University, Yonago, Tottori, Japan.
Ohira T; Department of Molecular and Cellular Biology, Division of Genome and Cellular Function, Tottori University, Yonago, Tottori, Japan.; Chromosome Engineering Research Center, Tottori University, Yonago, Tottori, Japan.
Shimizu R; Department of Molecular and Cellular Biology, Division of Genome and Cellular Function, Tottori University, Yonago, Tottori, Japan.; Division of Urology, Department of Surgery, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Morimoto M; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Murakami Y; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Hanaki T; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Kihara K; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Matsunaga T; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Yamamoto M; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Tokuyasu N; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Sakamoto T; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Fujiwara Y; Division of Gastrointestinal and Pediatric Surgery, Department of Surgery, School of Medicine, Faculty of Medicine, Tottori University, Yonago, Tottori, Japan.
Kugoh H; Department of Molecular and Cellular Biology, Division of Genome and Cellular Function, Tottori University, Yonago, Tottori, Japan. .; Chromosome Engineering Research Center, Tottori University, Yonago, Tottori, Japan. .
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Źródło:
Scientific reports [Sci Rep] 2021 Jul 28; Vol. 11 (1), pp. 15355. Date of Electronic Publication: 2021 Jul 28.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Loss of Heterozygosity*
Carcinogenesis/*genetics
Chimera/*genetics
Chromosomes, Human, Pair 3/*chemistry
Pancreatic Neoplasms/*genetics
Telomerase/*genetics
Animals ; Carcinogenesis/metabolism ; Carcinogenesis/pathology ; Cell Line, Tumor ; Cell Proliferation ; Chromosomes, Human, Pair 3/metabolism ; Gene Expression Regulation, Neoplastic ; Humans ; Mice ; Neoplasm Invasiveness ; Pancreatic Neoplasms/metabolism ; Pancreatic Neoplasms/pathology ; Promoter Regions, Genetic ; Telomerase/metabolism ; Transcription, Genetic
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Cerebral venous thrombosis with hyperhomocysteinemia due to loss of heterozygosity at methylenetetrahydrofolate reductase (MTHFR) locus: a case report.
Autorzy:
Zhang M; Department of Neurology, The First Medical Center, Chinese PLA General Hospital, No. 28 Fuxing Road, Beijing, 100853, PR China.
Shi B; Brain Science Center, Tsinghua University Yuquan Hospital, No. 5 Shijingshan Road, Beijing, 100049, PR China.
Zhao M; Brain Science Center, Tsinghua University Yuquan Hospital, No. 5 Shijingshan Road, Beijing, 100049, PR China. .
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Źródło:
BMC neurology [BMC Neurol] 2023 Apr 19; Vol. 23 (1), pp. 154. Date of Electronic Publication: 2023 Apr 19.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Hyperhomocysteinemia*/complications
Hyperhomocysteinemia*/genetics
Intracranial Thrombosis*/complications
Venous Thrombosis*/complications
Venous Thrombosis*/diagnostic imaging
Venous Thrombosis*/drug therapy
Female ; Humans ; Adolescent ; Methylenetetrahydrofolate Reductase (NADPH2)/genetics ; Heterozygote ; Folic Acid ; Loss of Heterozygosity ; Homocysteine ; Genotype
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Synchronous thyroid cancer and malignant struma ovarii: concordant mutations and microRNA profile, discordant loss of heterozygosity loci.
Autorzy:
Seo GT; Thyroid, Head and Neck Cancer (THANC) Foundation, 10 Union Square East, Suite 5B, New York, NY, 10003, USA.
Minkowitz J; Minkowitz Pathology, 904 49th Street, Brooklyn, NY, 11219, USA.; SUNY Downstate Medical Center, 450 Clarkson Avenue, Brooklyn, NY, 11203, USA.
Kapustin DA; Thyroid, Head and Neck Cancer (THANC) Foundation, 10 Union Square East, Suite 5B, New York, NY, 10003, USA. .; Department of Otolaryngology-Head and Neck Surgery, Icahn School of Medicine at Mount Sinai, 10 Union Square East, Suite 5B, New York, NY, 10003, USA. .
Fan J; Department of Pathology, Mount Sinai West Medical Center, 1000 10th Avenue, New York, NY, 10019, USA.
Minkowitz G; Minkowitz Pathology, 904 49th Street, Brooklyn, NY, 11219, USA.
Minkowitz M; Minkowitz Pathology, 904 49th Street, Brooklyn, NY, 11219, USA.
Dowling E; Department of Otolaryngology-Head and Neck Surgery, Icahn School of Medicine at Mount Sinai, 10 Union Square East, Suite 5B, New York, NY, 10003, USA.
Matloob A; Department of Pathology, Mount Sinai West Medical Center, 1000 10th Avenue, New York, NY, 10019, USA.
Asti D; Department of Hematology and Medical Oncology, Northwell Health Staten Island University Hospital, 475 Seaview Avenue, Staten Island, NY, 10305, USA.
Dhar M; Department of Hematology and Medical Oncology, Northwell Health Staten Island University Hospital, 475 Seaview Avenue, Staten Island, NY, 10305, USA.
Shutty C; Minkowitz Pathology, 904 49th Street, Brooklyn, NY, 11219, USA.
Brickman A; ParCare Community Health Network, 6010 Bay Parkway, Brooklyn, NY, 11204, USA.
Urken ML; Thyroid, Head and Neck Cancer (THANC) Foundation, 10 Union Square East, Suite 5B, New York, NY, 10003, USA.; Department of Otolaryngology-Head and Neck Surgery, Icahn School of Medicine at Mount Sinai, 10 Union Square East, Suite 5B, New York, NY, 10003, USA.
Brandwein-Weber M; Department of Pathology, Mount Sinai West Medical Center, 1000 10th Avenue, New York, NY, 10019, USA.
Finkelstein SD; Interpace Diagnostics, 2515 Liberty Ave, Pittsburgh, PA, 15222, USA.
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Źródło:
Diagnostic pathology [Diagn Pathol] 2023 Apr 18; Vol. 18 (1), pp. 47. Date of Electronic Publication: 2023 Apr 18.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Thyroid Neoplasms*/pathology
Struma Ovarii*/genetics
Struma Ovarii*/metabolism
Struma Ovarii*/pathology
Ovarian Neoplasms*/pathology
MicroRNAs*/genetics
Female ; Humans ; Adult ; Iodine Radioisotopes ; Proto-Oncogene Proteins B-raf/genetics ; Thyroid Cancer, Papillary/genetics ; Mutation ; Loss of Heterozygosity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Bi-allelic loss of function variant in the NRCAM gene is associated with motor-predominant axonal polyneuropathy; the second report.
Autorzy:
Elahi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran.
Soveyzi M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Nafissi S; Neuromuscular Research Center, Tehran University of Medical Sciences, Tehran, Iran.; Department of Neurology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Nilipour Y; Pediatric Pathology Research Center, Research Institute for Children's Health, Mofid Children Hospital, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Goleyjani Moghadam M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Keshavarz E; Department of Radiology, Mahdiyeh Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Kariminejad A; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran.
Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran.
Fattahi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Apr; Vol. 11 (4), pp. e2131. Date of Electronic Publication: 2023 Jan 06.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Neurodevelopmental Disorders*/genetics
Intellectual Disability*/genetics
Polyneuropathies*/genetics
Male ; Humans ; Phenotype ; Loss of Heterozygosity ; Cell Adhesion Molecules/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Ataxia-Telangiectasia Mutated Loss of Heterozygosity in Melanoma.
Autorzy:
Pastorino L; Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy.; Genetica dei Tumori Rari, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Dalmasso B; Genetica dei Tumori Rari, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Allavena E; Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy.
Vanni I; Genetica dei Tumori Rari, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Ugolini F; Section of Anatomic Pathology, Department of Health Sciences, University of Florence, 50134 Florence, Italy.
Baroni G; Section of Anatomic Pathology, Department of Health Sciences, University of Florence, 50134 Florence, Italy.
Croce M; Bioterapie, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Guadagno A; Anatomia Patologica, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Cabiddu F; Anatomia Patologica, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Andreotti V; Genetica dei Tumori Rari, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Bruno W; Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy.; Genetica dei Tumori Rari, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Zoppoli G; Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy.; Clinica di Medicina Interna a Indirizzo Oncologico, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Ferrando L; Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy.; Clinica di Medicina Interna a Indirizzo Oncologico, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Tanda ET; Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy.; Oncologia Medica 2, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Spagnolo F; Oncologia Medica 2, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Menin C; Immunology and Diagnostic Molecular Oncology Unit, Veneto Institute of Oncology, IOV-IRCCS, 35128 Padua, Italy.
Gangemi R; Bioterapie, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
Massi D; Section of Anatomic Pathology, Department of Health Sciences, University of Florence, 50134 Florence, Italy.
Ghiorzo P; Department of Internal Medicine and Medical Specialties, University of Genoa, 16132 Genoa, Italy.; Genetica dei Tumori Rari, IRCCS Ospedale Policlinico San Martino, 16132 Genoa, Italy.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Dec 16; Vol. 23 (24). Date of Electronic Publication: 2022 Dec 16.
Typ publikacji:
Journal Article
MeSH Terms:
Ataxia Telangiectasia*/genetics
Melanoma*/genetics
Humans ; Ataxia Telangiectasia Mutated Proteins/genetics ; DNA Copy Number Variations ; Loss of Heterozygosity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Cells with loss-of-heterozygosity after exposure to ionizing radiation in Drosophila are culled by p53-dependent and p53-independent mechanisms.
Autorzy:
Brown J; Department of Molecular, Cellular and Developmental Biology, 347 UCB, University of Colorado, Boulder, CO, United States of America.
Bush I; Department of Molecular, Cellular and Developmental Biology, 347 UCB, University of Colorado, Boulder, CO, United States of America.
Bozon J; Department of Molecular, Cellular and Developmental Biology, 347 UCB, University of Colorado, Boulder, CO, United States of America.
Su TT; Department of Molecular, Cellular and Developmental Biology, 347 UCB, University of Colorado, Boulder, CO, United States of America.
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Źródło:
PLoS genetics [PLoS Genet] 2020 Oct 19; Vol. 16 (10), pp. e1009056. Date of Electronic Publication: 2020 Oct 19 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Drosophila Proteins/*genetics
Drosophila melanogaster/*genetics
Loss of Heterozygosity/*genetics
Transcription Factors/*genetics
Tumor Suppressor Protein p53/*genetics
Alleles ; Animals ; Chromosome Aberrations/radiation effects ; Heterozygote ; Loss of Heterozygosity/radiation effects ; Mutation/genetics ; Radiation, Ionizing
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Involvement of Rev1 in alkylating agent-induced loss of heterozygosity in Oryzias latipes.
Autorzy:
Fujikawa Y; Radioisotope Research Center, Institute for Radiation Research, Osaka University, Suita, Japan.; Radiation Biology and Medical Genetics, Department of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Japan.; Japan Society for the Promotion of Science Research Fellow, Tokyo, Japan.
Ishikawa-Fujiwara T; Radioisotope Research Center, Institute for Radiation Research, Osaka University, Suita, Japan.; Radiation Biology and Medical Genetics, Department of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Japan.
Kuo T; RWBC-OIL, AIST, Tokyo, Japan.
Shinkai N; Artificial Intelligence Research Center (AIRC), AIST, Tokyo, Japan.; Cancer Translational Research Team, RIKEN Center for Advanced Intelligence Project, Tokyo, Japan.; Division of Molecular Modification and Cancer Biology, National Cancer Center Research Institute, Tokyo, Japan.
Shoji T; Artificial Intelligence Research Center (AIRC), AIST, Tokyo, Japan.; Humanome Lab., Inc., Tokyo, Japan.
Kawasaki T; Functional Biomolecular Research Group, Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Japan.
Kamei Y; Spectrography and Bioimaging Facility, National Institute for Basic Biology, Okazaki, Japan.
Sakuraba Y; Genomic Sciences Center (GSC), RIKEN Yokohama Institute, Yokohama, Japan.
Sato A; Department of Pathology, Hyogo College of Medicine, Nishinomiya, Japan.
Kinoshita M; Division of Applied Bioscience, Graduate School of Agriculture, Kyoto University, Kyoto, Japan.
Gondo Y; Genomic Sciences Center (GSC), RIKEN Yokohama Institute, Yokohama, Japan.
Yuba S; Functional Biomolecular Research Group, Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Japan.
Tsujimura T; Department of Pathology, Hyogo College of Medicine, Nishinomiya, Japan.
Sese J; RWBC-OIL, AIST, Tokyo, Japan.; Artificial Intelligence Research Center (AIRC), AIST, Tokyo, Japan.; Humanome Lab., Inc., Tokyo, Japan.
Todo T; Radioisotope Research Center, Institute for Radiation Research, Osaka University, Suita, Japan.; Radiation Biology and Medical Genetics, Department of Genome Biology, Graduate School of Medicine, Osaka University, Suita, Japan.
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Źródło:
Genes to cells : devoted to molecular & cellular mechanisms [Genes Cells] 2020 Feb; Vol. 25 (2), pp. 124-138. Date of Electronic Publication: 2020 Feb 05.
Typ publikacji:
Journal Article
MeSH Terms:
Loss of Heterozygosity*
Nucleotidyltransferases/*genetics
Nucleotidyltransferases/*metabolism
Oryzias/*genetics
Animals ; Animals, Genetically Modified ; Carcinogenesis ; Cell Line ; DNA Damage ; DNA Repair ; DNA Replication ; DNA-Directed DNA Polymerase ; Female ; Gene Expression Regulation ; Liver/pathology ; Male ; Mutagenesis ; Mutation ; Recombinant Proteins ; Transcriptome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Heterozygous loss of Rbm24 in the adult mouse heart increases sarcomere slack length but does not affect function.
Autorzy:
de Groot NE; Department of Experimental Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, location AMC, Amsterdam, The Netherlands.
van den Hoogenhof MMG; Department of Experimental Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, location AMC, Amsterdam, The Netherlands.
Najafi A; Department of Physiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
van der Made I; Department of Experimental Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, location AMC, Amsterdam, The Netherlands.
van der Velden J; Department of Physiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Beqqali A; Department of Experimental Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, location AMC, Amsterdam, The Netherlands.
Pinto YM; Department of Experimental Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, location AMC, Amsterdam, The Netherlands.
Creemers EE; Department of Experimental Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, location AMC, Amsterdam, The Netherlands. .
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Źródło:
Scientific reports [Sci Rep] 2020 May 06; Vol. 10 (1), pp. 7687. Date of Electronic Publication: 2020 May 06.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Loss of Heterozygosity*
Myocardium/*metabolism
RNA-Binding Proteins/*genetics
Sarcomeres/*metabolism
Animals ; Biomarkers ; Cell Membrane/metabolism ; Cell Membrane Permeability ; Disease Models, Animal ; Echocardiography ; Heart Diseases/diagnostic imaging ; Heart Diseases/genetics ; Heart Diseases/metabolism ; Immunohistochemistry ; Isometric Contraction ; Mice ; Mice, Knockout ; Myocytes, Cardiac/metabolism ; RNA-Binding Proteins/metabolism ; Sarcomeres/ultrastructure
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Calorie restriction alters the mechanisms of radiation-induced mouse thymic lymphomagenesis.
Autorzy:
Nakayama T; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.; Department of Tumor and Diagnostic Pathology, Atomic Bomb Disease Institute, Nagasaki University, Nagasaki, Japan.; Graduate School of Science and Engineering, Ibaraki University, Mito, Japan.
Sunaoshi M; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.
Shang Y; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.
Takahashi M; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.; Graduate School of Science and Engineering, Ibaraki University, Mito, Japan.
Saito T; Graduate School of Science and Engineering, Ibaraki University, Mito, Japan.
Blyth BJ; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.
Amasaki Y; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.
Daino K; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.
Shimada Y; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.
Tachibana A; Graduate School of Science and Engineering, Ibaraki University, Mito, Japan.
Kakinuma S; Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum Science and Technology, Chiba, Japan.
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Źródło:
PloS one [PLoS One] 2023 Jan 20; Vol. 18 (1), pp. e0280560. Date of Electronic Publication: 2023 Jan 20 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Thymus Neoplasms*/genetics
Neoplasms, Radiation-Induced*/genetics
Mice ; Animals ; Caloric Restriction ; Mutation ; Point Mutation ; Alleles ; Loss of Heterozygosity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Detection of Loss of Heterozygosity in cfDNA of Advanced EGFR - or KRAS -Mutated Non-Small-Cell Lung Cancer Patients.
Autorzy:
Boldrin E; Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV-IRCCS, Via Gattamelata 64, 35128 Padova, Italy.
Nardo G; Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV-IRCCS, Via Gattamelata 64, 35128 Padova, Italy.
Zulato E; Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV-IRCCS, Via Gattamelata 64, 35128 Padova, Italy.
Bonanno L; Medical Oncology 2, Istituto Oncologico Veneto IOV-IRCCS, Via Gattamelata 64, 35128 Padova, Italy.
Polo V; Medical Oncology, Azienda ULSS 2, 31100 Treviso, Italy.
Frega S; Medical Oncology 2, Istituto Oncologico Veneto IOV-IRCCS, Via Gattamelata 64, 35128 Padova, Italy.
Pavan A; Medical Oncology 2, Istituto Oncologico Veneto IOV-IRCCS, Via Gattamelata 64, 35128 Padova, Italy.
Indraccolo S; Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV-IRCCS, Via Gattamelata 64, 35128 Padova, Italy.
Saggioro D; Immunology and Molecular Oncology Unit, Istituto Oncologico Veneto IOV-IRCCS, Via Gattamelata 64, 35128 Padova, Italy.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2019 Dec 20; Vol. 21 (1). Date of Electronic Publication: 2019 Dec 20.
Typ publikacji:
Journal Article
MeSH Terms:
Loss of Heterozygosity*
Carcinoma, Non-Small-Cell Lung/*genetics
Cell-Free Nucleic Acids/*genetics
Lung Neoplasms/*genetics
Proto-Oncogene Proteins p21(ras)/*genetics
Aged ; Aged, 80 and over ; Carcinoma, Non-Small-Cell Lung/pathology ; ErbB Receptors/genetics ; Female ; Humans ; Lung Neoplasms/pathology ; Male ; Middle Aged ; Mutation ; Pilot Projects
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Single-Gene Deletions Contributing to Loss of Heterozygosity in Saccharomyces cerevisiae : Genome-Wide Screens and Reproducibility.
Autorzy:
Hoffert KM; Department of Biological Sciences, Northern Kentucky University, Highland Heights, Kentucky, 41099.
Strome ED; Department of Biological Sciences, Northern Kentucky University, Highland Heights, Kentucky, 41099 .
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Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2019 Sep 04; Vol. 9 (9), pp. 2835-2850. Date of Electronic Publication: 2019 Sep 04.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Gene Deletion*
Genomic Instability*
Loss of Heterozygosity*
Saccharomyces cerevisiae/*genetics
Saccharomyces cerevisiae Proteins/*genetics
Chromosomes, Fungal ; Cysteine Synthase/genetics ; Gene Ontology ; Genome, Fungal ; Haploinsufficiency/genetics ; Humans ; Neoplasms/genetics ; Reproducibility of Results
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Epigenetic loss of heterozygosity of Apc and an inflammation-associated mutational signature detected in Lrig1 -driven murine colonic adenomas.
Autorzy:
Preston JL; Institute of Molecular Biology, University of Oregon, Eugene, OR, 97403, USA. .
Stiffler N; Institute of Molecular Biology, University of Oregon, Eugene, OR, 97403, USA.
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Źródło:
BMC cancer [BMC Cancer] 2020 Feb 14; Vol. 20 (1), pp. 126. Date of Electronic Publication: 2020 Feb 14.
Typ publikacji:
Journal Article
MeSH Terms:
Epigenesis, Genetic*
Genes, APC*
Loss of Heterozygosity*
Mutation*
Colonic Neoplasms/*genetics
Membrane Glycoproteins/*genetics
Nerve Tissue Proteins/*genetics
Animals ; Cell Transformation, Neoplastic/genetics ; Disease Models, Animal ; Exome ; Gene Expression Profiling ; Gene Silencing ; Humans ; Mice ; Transcriptome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Heterozygous loss of Srp72 in mice is not associated with major hematological phenotypes.
Autorzy:
D'Altri T; The Finsen Laboratory, Rigshospitalet, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.; Biotech Research and Innovation Centre (BRIC), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.; Danish Stem Cell Centre (DanStem), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
Schuster MB; The Finsen Laboratory, Rigshospitalet, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.; Biotech Research and Innovation Centre (BRIC), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.; Danish Stem Cell Centre (DanStem), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
Wenzel A; The Finsen Laboratory, Rigshospitalet, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.; Biotech Research and Innovation Centre (BRIC), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.; Danish Stem Cell Centre (DanStem), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
Porse BT; The Finsen Laboratory, Rigshospitalet, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.; Biotech Research and Innovation Centre (BRIC), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.; Danish Stem Cell Centre (DanStem), Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.
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Źródło:
European journal of haematology [Eur J Haematol] 2019 Oct; Vol. 103 (4), pp. 319-328. Date of Electronic Publication: 2019 Jul 26.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Association Studies*
Genetic Predisposition to Disease*
Loss of Heterozygosity*
Mutation*
Phenotype*
Hematopoiesis/*genetics
Signal Recognition Particle/*genetics
Animals ; Biomarkers ; Blood Cell Count ; Bone Marrow/pathology ; Disease Models, Animal ; Gene Editing ; Gene Expression ; Genes, Lethal ; Genotype ; Mice ; Mice, Knockout
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 5345

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