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Wyszukujesz frazę ""Chromosomes, Human, Pair 1"" wg kryterium: Temat


Tytuł:
FSTest: an efficient tool for cross-population fixation index estimation on variant call format files.
Autorzy:
Vahedi SM; Department of Animal Science and Aquaculture, Dalhousie University, Bible Hill, NS B2N5E3, .
Ardestani SS
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Źródło:
Journal of genetics [J Genet] 2024; Vol. 103.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*/genetics
Genetics, Population*/methods
Genetics, Population*/statistics & numerical data
South Asian People*/genetics
African People*/genetics
Genetic Variation*/genetics
Humans ; Asian People/genetics ; Biological Evolution ; Genomics ; Genotype
Czasopismo naukowe
Tytuł:
Alterations in chromosome 1q in multiple myeloma randomized clinical trials: a systematic review.
Autorzy:
Neupane K; Department of Internal Medicine, Albert Einstein College of Medicine/Jacobi Medical Center, Bronx, NY, USA.
Fortuna GG; Division of Hematology and Hematological Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Dahal R; Department of Internal Medicine, Universal College of Medical Sciences, Siddharthanagar, Nepal.
Schmidt T; Department of Hematology-Oncology, University of Wisconsin, Madison, WI, USA.
Fonseca R; Department of Hematology-Oncology, Mayo Clinic, Phoenix, AZ, USA.
Chakraborty R; Department of Hematology and Oncology, Columbia University Herbert Irving Comprehensive Cancer Center, New York, NY, USA.
Koehn KA; Department of Hematology and Oncology, Chub O'Reilly Cancer Center, Springfield, MO, USA.
Mohan M; Department of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI, US.
Mian H; Department of Hematology and Oncology, McMaster University, Hamilton, ON, Canada.
Costa LJ; Department of Hematology and Oncology, O'Neal Cancer Center, University of Alabama, Birmingham, AL, USA.
Sborov D; Division of Hematology and Hematological Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Mohyuddin GR; Division of Hematology and Hematological Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA. .
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Źródło:
Blood cancer journal [Blood Cancer J] 2024 Jan 25; Vol. 14 (1), pp. 20. Date of Electronic Publication: 2024 Jan 25.
Typ publikacji:
Systematic Review; Journal Article
MeSH Terms:
Multiple Myeloma*/drug therapy
Multiple Myeloma*/genetics
Humans ; Bortezomib/therapeutic use ; Lenalidomide/therapeutic use ; Prognosis ; Chromosome Aberrations ; Chromosomes, Human, Pair 1/genetics ; Antineoplastic Combined Chemotherapy Protocols
Czasopismo naukowe
Tytuł:
A de novo variant in ZBTB18 gene caused autosomal dominant non-syndromic intellectual disability 22 syndrome: A case report and literature review.
Autorzy:
Yang F; Clinical Research Ward, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ding Y; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Wang Y; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Zhang Q; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Li H; Clinical Research Ward, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.; Department of Pharmacy, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yu T; Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Chang G; Clinical Research Ward, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Wang X; Clinical Research Ward, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.; Department of Endocrinology and Metabolism, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
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Źródło:
Medicine [Medicine (Baltimore)] 2024 Jan 12; Vol. 103 (2), pp. e35908.
Typ publikacji:
Review; Case Reports; Journal Article
MeSH Terms:
Intellectual Disability*/diagnosis
Intellectual Disability*/genetics
Nervous System Malformations*/genetics
Child ; Humans ; Male ; Abnormalities, Multiple/genetics ; Chromosome Deletion ; Chromosomes, Human, Pair 1 ; Microcephaly/genetics ; Repressor Proteins/genetics
SCR Disease Name:
Chromosome 1q43-Q44 Deletion Syndrome
Czasopismo naukowe
Tytuł:
Strong selection signatures for Aleutian disease tolerance acting on novel candidate genes linked to immune and cellular responses in American mink (Neogale vison).
Autorzy:
Vahedi SM; Department of Animal Science and Aquaculture, Dalhousie University, Bible Hill, NS, B2N5E3, Canada.
Salek Ardestani S; Department of Animal Science, University of Zanjan, Zanjan, 4537138791, Zanjan, Iran.
Banabazi MH; Department of Animal Breeding and Genetics (HGEN), Centre for Veterinary Medicine and Animal Science (VHC), Swedish University of Agricultural Sciences (SLU), 75007, Uppsala, Sweden. .; Department of Biotechnology, Animal Science Research Institute of IRAN (ASRI),, Agricultural Research, Education & Extension Organization (AREEO), Karaj, 3146618361, Iran. .
Clark KF; Department of Animal Science and Aquaculture, Dalhousie University, Bible Hill, NS, B2N5E3, Canada. .
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Źródło:
Scientific reports [Sci Rep] 2024 Jan 10; Vol. 14 (1), pp. 1035. Date of Electronic Publication: 2024 Jan 10.
Typ publikacji:
Journal Article
MeSH Terms:
Aleutian Mink Disease*/genetics
Aleutian Mink Disease Virus*/genetics
Animals ; Humans ; Mink/genetics ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 6
Czasopismo naukowe
Tytuł:
Exploiting nanopore sequencing for characterization and grading of IDH-mutant gliomas.
Autorzy:
Wongsurawat T; Division of Medical Bioinformatics, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.; Department of Biomedical Informatics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Jenjaroenpun P; Division of Medical Bioinformatics, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.; Department of Biomedical Informatics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Anekwiang P; Department of Medicine (Neurology), Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Arigul T; Division of Medical Bioinformatics, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Thongrattana W; Division of Medical Bioinformatics, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Jamshidi-Parsian A; Department of Radiation Oncology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Boysen G; Department of Environmental and Occupational Health, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Suriyaphol P; Division of Medical Bioinformatics, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Suktitipat B; Division of Medical Bioinformatics, Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.; Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Srirabheebhat P; Department of Surgery (Neurosurgery), Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Cheunsuchon P; Department of Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Tanboon J; Department of Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Nookaew I; Department of Biomedical Informatics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Sathornsumetee S; Department of Medicine (Neurology), Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
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Źródło:
Brain pathology (Zurich, Switzerland) [Brain Pathol] 2024 Jan; Vol. 34 (1), pp. e13203. Date of Electronic Publication: 2023 Aug 13.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:
Oligodendroglioma*/genetics
Oligodendroglioma*/pathology
Brain Neoplasms*/pathology
Nanopore Sequencing*
Glioma*/pathology
Astrocytoma*/pathology
Humans ; Mutation ; Isocitrate Dehydrogenase/genetics ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 19
Czasopismo naukowe
Tytuł:
Effects of Aegilops longissima chromosome 1S on wheat bread-making quality in two types of translocation lines.
Autorzy:
Qiu Y; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.; Institute of Cotton Sciences, Shanxi Agricultural University, Yuncheng, 044000, China.
Han Z; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Liu N; Keshan Branch, Heilongjiang Academy of Agricultural Sciences, Qiqihar, 161600, China.
Yu M; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Zhang S; Crop Research Institute, Ningxia Academy of Agri-Forestry Sciences, Yinchuan, 750105, China.
Chen H; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Tang H; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Zhao Z; Institute of Cotton Sciences, Shanxi Agricultural University, Yuncheng, 044000, China.
Wang K; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Lin Z; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Han F; Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China. .
Ye X; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China. .
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Źródło:
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik [Theor Appl Genet] 2023 Dec 10; Vol. 137 (1), pp. 2. Date of Electronic Publication: 2023 Dec 10.
Typ publikacji:
Journal Article
MeSH Terms:
Triticum*/genetics
Triticum*/metabolism
Aegilops*/genetics
Aegilops*/metabolism
Humans ; Translocation, Genetic ; Bread/analysis ; Chromosomes, Human, Pair 1/metabolism ; Glutens/genetics ; Glutens/metabolism
Czasopismo naukowe
Tytuł:
Rapid intraoperative multi-molecular diagnosis of glioma with ultrasound radio frequency signals and deep learning.
Autorzy:
Xie X; School of Information Science and Technology, Fudan University, Shanghai, China; Neurosurgical Institute of Fudan University, Shanghai, China.
Shen C; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China; National Center for Neurological Disorders, Shanghai, China; Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Shanghai, China; Neurosurgical Institute of Fudan University, Shanghai, China.
Zhang X; Department of Ultrasound, Huashan Hospital, Fudan University, Shanghai, China.
Wu G; School of Information Science and Technology, Fudan University, Shanghai, China; Neurosurgical Institute of Fudan University, Shanghai, China.
Yang B; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China; National Center for Neurological Disorders, Shanghai, China; Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Shanghai, China; Neurosurgical Institute of Fudan University, Shanghai, China.
Qi Z; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China; National Center for Neurological Disorders, Shanghai, China; Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Shanghai, China; Neurosurgical Institute of Fudan University, Shanghai, China.
Tang Q; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China; National Center for Neurological Disorders, Shanghai, China; Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Shanghai, China; Neurosurgical Institute of Fudan University, Shanghai, China.
Wang Y; School of Information Science and Technology, Fudan University, Shanghai, China.
Ding H; Department of Ultrasound, Huashan Hospital, Fudan University, Shanghai, China. Electronic address: ding_.
Shi Z; Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China; National Center for Neurological Disorders, Shanghai, China; Shanghai Key Laboratory of Brain Function Restoration and Neural Regeneration, Shanghai, China; Neurosurgical Institute of Fudan University, Shanghai, China. Electronic address: .
Yu J; School of Information Science and Technology, Fudan University, Shanghai, China; Neurosurgical Institute of Fudan University, Shanghai, China. Electronic address: .
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Źródło:
EBioMedicine [EBioMedicine] 2023 Dec; Vol. 98, pp. 104899. Date of Electronic Publication: 2023 Dec 02.
Typ publikacji:
Journal Article
MeSH Terms:
Deep Learning*
Glioma*/diagnostic imaging
Glioma*/genetics
Brain Neoplasms*/diagnostic imaging
Brain Neoplasms*/genetics
Humans ; Retrospective Studies ; Prospective Studies ; Mutation ; Biomarkers, Tumor/genetics ; Isocitrate Dehydrogenase/genetics ; Chromosomes, Human, Pair 1
Czasopismo naukowe
Tytuł:
Independent prognostic impact of DNA methylation class and chromosome 1p loss in WHO grade 2 and 3 meningioma undergoing adjuvant high-dose radiotherapy: comprehensive molecular analysis of EORTC 22042-26042.
Autorzy:
Maas SLN; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands.; Department of Pathology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Sievers P; Department of Neuropathology, Institute of Pathology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany.; CCU Neuropathology, German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Weber DC; Paul Scherrer Institute, Villigen PSI, Switzerland.; Department of Radiation Oncology, University Hospital and University of Zurich, Zurich, Switzerland.
Weller M; Department of Neurology, Clinical Neuroscience Center, University Hospital and University of Zurich, Zurich, Switzerland.
van den Bent MJ; The Brain Tumor Center, Erasmus Medical Center Cancer Institute, Rotterdam, The Netherlands.
Mair MJ; Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Kros JM; Department of Pathology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Carparrotti F; Hôpitaux Universitaires de Genève, Geneva, Switzerland.
von Deimling A; Department of Neuropathology, Institute of Pathology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany.; CCU Neuropathology, German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.
Salvador VF; ICO Badalona, Hospital Germans Trias I Pujol (Institut Catala D'Oncologia), Catalonia, Spain.
Peerdeman SM; Department of Neurosurgery, Amsterdam UMC, Amsterdam, The Netherlands.
Casas-Martin J; EORTC Head Quarters, Brussels, Belgium.
Gorlia T; EORTC Head Quarters, Brussels, Belgium.
Sahm F; Department of Neuropathology, Institute of Pathology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany. .; CCU Neuropathology, German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany. .
Preusser M; Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
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Źródło:
Acta neuropathologica [Acta Neuropathol] 2023 Dec; Vol. 146 (6), pp. 837-840. Date of Electronic Publication: 2023 Oct 19.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Meningioma*/genetics
Meningioma*/radiotherapy
Meningeal Neoplasms*/genetics
Meningeal Neoplasms*/radiotherapy
Humans ; Prognosis ; DNA Methylation ; Chromosome Deletion ; Chromosomes ; World Health Organization ; Chromosomes, Human, Pair 1/genetics
Czasopismo naukowe
Tytuł:
mTOR eosinophilic renal cell carcinoma: a distinctive tumor characterized by mTOR mutation, loss of chromosome 1, cathepsin-K expression, and response to target therapy.
Autorzy:
Caliò A; Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy.
Marletta S; Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy.; Department of Pathology, Pederzoli Hospital, Peschiera del Garda, Italy.
Settanni G; Department of Pathology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar, Italy.
Rizzo M; Division of Medical Oncology, A.O.U. Consorziale Policlinico Di Bari, Bari, Italy.
Gobbo S; Department of Translational Medicine, University of Ferrara, Ferrara, Italy.
Pedron S; Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy.
Stefanizzi L; Department of Pathology, Pederzoli Hospital, Peschiera del Garda, Italy.
Munari E; Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Brunelli M; Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy.
Marcolini L; Department of Pathology, Pederzoli Hospital, Peschiera del Garda, Italy.
Pesci A; Department of Pathology, IRCCS Sacro Cuore Don Calabria Hospital, Negrar, Italy.
Fratoni S; Division of Anatomic Pathology, S. Eugenio Hospital, Rome, Italy.
Pierconti F; Division of Anatomic Pathology and Histology, Foundation 'A. Gemelli' University Hospital, Università Cattolica del Sacro Cuore, Rome, Italy.
Raspollini MR; Histopathology and Molecular Diagnostics, Azienda Ospedaliero Universitaria Careggi, Florence, Italy.
Marchetti A; Division of Anatomic Pathology and Histology, Ospedale Clinicizzato 'SS. Annunziata' Università Di Chieti, Chieti, Italy.
Doglioni C; Department of Pathology, San Raffaele Hospital, Milan, Italy.
Amin MB; Department of Pathology and Laboratory Medicine, University of Tennessee Health Science, Memphis, TN, USA.; Department of Urology, USC Keck School of Medicine, Los Angeles, CA, USA.
Porta C; Interdisciplinary Department of Medicine, University of Bari 'A. Moro, Bari, Italy.
Martignoni G; Department of Diagnostic and Public Health, Section of Pathology, University of Verona, Largo L. Scuro 10, 37134, Verona, Italy. .; Department of Pathology, Pederzoli Hospital, Peschiera del Garda, Italy. .
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Źródło:
Virchows Archiv : an international journal of pathology [Virchows Arch] 2023 Dec; Vol. 483 (6), pp. 821-833. Date of Electronic Publication: 2023 Nov 08.
Typ publikacji:
Journal Article
MeSH Terms:
Carcinoma, Renal Cell*/drug therapy
Carcinoma, Renal Cell*/genetics
Carcinoma, Renal Cell*/metabolism
Kidney Neoplasms*/drug therapy
Kidney Neoplasms*/genetics
Kidney Neoplasms*/metabolism
Liver Neoplasms*/drug therapy
Liver Neoplasms*/genetics
Humans ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Chromosomes, Human, Pair 1/metabolism ; MTOR Inhibitors ; Mutation ; TOR Serine-Threonine Kinases/genetics
Czasopismo naukowe
Tytuł:
Deletion in 1p36.33-p36.32 is associated with pancytopenia: a case report.
Autorzy:
Yang H; Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China.; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Huang J; Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China.; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Zheng H; Department of Pediatrics, Fujian Union Hospital, Fuzhou, China.
Zhang Y; Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China.; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Zhang Y; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.; Department of Pediatrics, Affiliated Dongfang Hospital, Xiamen University, Fuzhou, China.
Liu W; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Wu J; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Chen X; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Lin J; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Ni Y; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Nie X; Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China. .; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China. .; Department of Pediatrics, Affiliated Dongfang Hospital, Xiamen University, Fuzhou, China. .
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Źródło:
BMC medical genomics [BMC Med Genomics] 2023 Nov 09; Vol. 16 (1), pp. 282. Date of Electronic Publication: 2023 Nov 09.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Intellectual Disability*/genetics
Pancytopenia*/genetics
Chromosome Disorders*/genetics
Humans ; DNA Copy Number Variations ; Chromosome Deletion ; Syndrome ; Phenotype ; Chromosomes, Human, Pair 1
SCR Disease Name:
Chromosome 1p36 Deletion Syndrome
Czasopismo naukowe
Tytuł:
Evaluation of chromosome 1p/19q deletion by Fluorescence in Situ Hybridization (FISH) as prognostic factors in malignant glioma patients on treatment with alkylating chemotherapy.
Autorzy:
Pandith AA; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J & K, India. Electronic address: .
Zahoor W; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J & K, India.
Manzoor U; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J & K, India.
Nisar S; Department of Medical Oncology, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
Guru FR; Department of Medical Oncology, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
Naikoo NA; Department of Biotechnology, Higher Education Department, Cluster University, Srinagar, J & K, India.
Aein QU; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J & K, India.
Baba SM; Advanced Centre for Human Genetics, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J & K, India.
Bhat AR; Department of Neurosurgery, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
Ganai F; Department of CVTS, Sher-I-Kashmir Institute of Medical Sciences (SKIMS), Srinagar, J&K, India.
Shah P; Department of Pathology, SKIMS, Srinagar, J & K, India.
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Źródło:
Cancer genetics [Cancer Genet] 2023 Nov; Vol. 278-279, pp. 55-61. Date of Electronic Publication: 2023 Aug 10.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Brain Neoplasms*/drug therapy
Brain Neoplasms*/genetics
Brain Neoplasms*/pathology
Glioma*/drug therapy
Glioma*/genetics
Glioma*/pathology
Oligodendroglioma*/drug therapy
Oligodendroglioma*/genetics
Oligodendroglioma*/pathology
Astrocytoma*/genetics
Humans ; Prognosis ; In Situ Hybridization, Fluorescence ; Chromosome Deletion ; Chromosome Aberrations ; Chromosomes ; Chromosomes, Human, Pair 1/genetics ; Chromosomes, Human, Pair 19/genetics
Czasopismo naukowe
Tytuł:
Chromosome 1p36 candidate gene ZNF436 predicts the prognosis of neuroblastoma: a bioinformatic analysis.
Autorzy:
Wang H; Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China. .
Wang X; Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
Xu L; Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
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Źródło:
Italian journal of pediatrics [Ital J Pediatr] 2023 Oct 31; Vol. 49 (1), pp. 145. Date of Electronic Publication: 2023 Oct 31.
Typ publikacji:
Journal Article
MeSH Terms:
Neuroblastoma*/genetics
Humans ; Infant ; Adolescent ; N-Myc Proto-Oncogene Protein/genetics ; Prognosis ; Chromosome Aberrations ; Chromosomes ; Chromosomes, Human, Pair 1/genetics ; Chromosome Deletion ; Transcription Factors/genetics
Czasopismo naukowe
Tytuł:
Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment.
Autorzy:
Kivrak Pfiffner F; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Koller S; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Ménétrey A; Department of Pediatric Neurology, University Children's Hospital, University of Zurich, 8032 Zurich, Switzerland.
Graf U; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Bähr L; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Maspoli A; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Hackenberg A; Department of Pediatric Neurology, University Children's Hospital, University of Zurich, 8032 Zurich, Switzerland.
Kottke R; Department of Diagnostic Imaging, University Children's Hospital, University of Zurich, 8032 Zurich, Switzerland.
Gerth-Kahlert C; Department of Ophthalmology, University Hospital, 8091 Zurich, Switzerland.
Berger W; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.; Neuroscience Center Zurich, University and ETH Zurich, 8057 Zurich, Switzerland.; Center for Integrative Human Physiology, University of Zurich, 8057 Zurich, Switzerland.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Jul 02; Vol. 23 (13). Date of Electronic Publication: 2022 Jul 02.
Typ publikacji:
Case Reports
MeSH Terms:
Chromosomes, Human, Pair 1*
Uniparental Disomy*
Female ; GTPase-Activating Proteins/genetics ; Guanine Nucleotide Exchange Factors/genetics ; Humans ; Infant ; Polymorphism, Single Nucleotide ; Spasms, Infantile ; Vision Disorders
SCR Disease Name:
Infantile Epileptic-Dyskinetic Encephalopathy
Raport
Tytuł:
CRISPR imaging reveals chromatin fluctuation at the centromere region related to cellular senescence.
Autorzy:
Takata H; Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka, 563-8577, Japan. .
Masuda Y; Graduate School of Human Development and Environment, Kobe University, Nada-ku, Kobe, 657-8501, Japan.
Ohmido N; Graduate School of Human Development and Environment, Kobe University, Nada-ku, Kobe, 657-8501, Japan.
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Źródło:
Scientific reports [Sci Rep] 2023 Sep 05; Vol. 13 (1), pp. 14609. Date of Electronic Publication: 2023 Sep 05.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromatin*
Clustered Regularly Interspaced Short Palindromic Repeats*
Humans ; Centromere ; Cellular Senescence ; Chromosomes, Human, Pair 1 ; Decitabine
Czasopismo naukowe
Tytuł:
Tandem NBPF 3mer HORs (Olduvai triplets) in Neanderthal and two novel HOR tandem arrays in human chromosome 1 T2T-CHM13 assembly.
Autorzy:
Glunčić M; Faculty of Science, University of Zagreb, 10000, Zagreb, Croatia. .
Vlahović I; Algebra University College, 10000, Zagreb, Croatia.
Rosandić M; University Hospital Centre Zagreb (Ret.), 10000, Zagreb, Croatia.; Croatian Academy of Sciences and Arts, 10000, Zagreb, Croatia.
Paar V; Faculty of Science, University of Zagreb, 10000, Zagreb, Croatia.; Croatian Academy of Sciences and Arts, 10000, Zagreb, Croatia.
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Źródło:
Scientific reports [Sci Rep] 2023 Sep 02; Vol. 13 (1), pp. 14420. Date of Electronic Publication: 2023 Sep 02.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Neanderthals*/genetics
Neuroblastoma*
Humans ; Animals ; Chromosomes, Human ; Chromosomes, Human, Pair 1 ; Family ; Pan troglodytes
Czasopismo naukowe
Tytuł:
Clonal cytopenia of undetermined significance presenting with multiple duplications of chromosome 1q.
Autorzy:
Wang P; SINO-US Diagnostics, Tianjin Enterprise Key Laboratory of AI-Aided Hematopathology Diagnosis, Tianjin, 300385, China.
Yang S; SINO-US Diagnostics, Tianjin Enterprise Key Laboratory of AI-Aided Hematopathology Diagnosis, Tianjin, 300385, China. .
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Źródło:
International journal of hematology [Int J Hematol] 2023 Sep; Vol. 118 (3), pp. 307-308. Date of Electronic Publication: 2023 Jul 14.
Typ publikacji:
Journal Article
MeSH Terms:
Myelodysplastic Syndromes*/genetics
Multiple Myeloma*/genetics
Anemia*
Humans ; Clonal Hematopoiesis ; Chromosomes, Human, Pair 1/genetics ; Chromosome Aberrations
Czasopismo naukowe
Tytuł:
Recurrent atypical teratoid/rhabdoid tumors (AT/RT) reveal discrete features of progression on histology, epigenetics, copy number profiling, and transcriptomics.
Autorzy:
Johann PD; Paediatric and Adolescent Medicine, Swabian Children's Cancer Center Augsburg, EU-RHAB Trial Center, Germany and Bavarian Cancer Research Center (BZKF), Augsburg, Germany.; Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.; Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ) and German Cancer Research Consortium (DKTK), Heidelberg, Germany.
Altendorf L; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Research Institute Children's Cancer Center Hamburg, Martinistraße 52, N63, 20251, Hamburg, Germany.
Efremova EM; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Research Institute Children's Cancer Center Hamburg, Martinistraße 52, N63, 20251, Hamburg, Germany.
Holsten T; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Research Institute Children's Cancer Center Hamburg, Martinistraße 52, N63, 20251, Hamburg, Germany.; Institute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Steinbügl M; Paediatric and Adolescent Medicine, Swabian Children's Cancer Center Augsburg, EU-RHAB Trial Center, Germany and Bavarian Cancer Research Center (BZKF), Augsburg, Germany.
Nemes K; Paediatric and Adolescent Medicine, Swabian Children's Cancer Center Augsburg, EU-RHAB Trial Center, Germany and Bavarian Cancer Research Center (BZKF), Augsburg, Germany.
Eckhardt A; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Research Institute Children's Cancer Center Hamburg, Martinistraße 52, N63, 20251, Hamburg, Germany.; Department of Radiotherapy and Radio-Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Kresbach C; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Research Institute Children's Cancer Center Hamburg, Martinistraße 52, N63, 20251, Hamburg, Germany.; Institute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Mildred Scheel Cancer Career Center HaTriCS4, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Bockmayr M; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Research Institute Children's Cancer Center Hamburg, Martinistraße 52, N63, 20251, Hamburg, Germany.; Mildred Scheel Cancer Career Center HaTriCS4, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Koch A; Institute of Neuropathology, Charité, Universitätsmedizin Berlin, Berlin, Germany.
Haberler C; Institute of Neurology, Medical University of Vienna, Vienna, Austria.; Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Antonelli M; Department of Radiological, Oncological and Anatomic Pathology Sciences, Università Sapienza, Rome, Italy.
DeSisto J; Morgan Adams Foundation Pediatric Brain Tumor Research Program, Children's Hospital Colorado, Aurora, CO, USA.
Schuhmann MU; Division of Pediatric Neurosurgery, Department of Neurosurgery, Eberhard Karl's University Hospital of Tübingen, Tübingen, Germany.
Hauser P; Second Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Siebert R; Institute of Human Genetics, Ulm University & Ulm University Medical Center, Ulm, Germany.
Bens S; Institute of Human Genetics, Ulm University & Ulm University Medical Center, Ulm, Germany.
Kool M; Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.; Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ) and German Cancer Research Consortium (DKTK), Heidelberg, Germany.; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Green AL; Morgan Adams Foundation Pediatric Brain Tumor Research Program, Children's Hospital Colorado, Aurora, CO, USA.; Department of Pediatrics, University of Colorado Denver, Aurora, CO, USA.
Hasselblatt M; Institute of Neuropathology, University Hospital Münster, Münster, Germany.
Frühwald MC; Paediatric and Adolescent Medicine, Swabian Children's Cancer Center Augsburg, EU-RHAB Trial Center, Germany and Bavarian Cancer Research Center (BZKF), Augsburg, Germany.
Schüller U; Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. .; Research Institute Children's Cancer Center Hamburg, Martinistraße 52, N63, 20251, Hamburg, Germany. .; Institute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. .
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Źródło:
Acta neuropathologica [Acta Neuropathol] 2023 Sep; Vol. 146 (3), pp. 527-541. Date of Electronic Publication: 2023 Jul 14.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Disease Progression*
DNA Copy Number Variations*/genetics
Epigenesis, Genetic*
Gene Expression Profiling*
Recurrence*
Rhabdoid Tumor*/classification
Rhabdoid Tumor*/genetics
Rhabdoid Tumor*/immunology
Rhabdoid Tumor*/pathology
Teratoma*/classification
Teratoma*/genetics
Teratoma*/immunology
Teratoma*/pathology
Child ; Child, Preschool ; Female ; Humans ; Infant ; Male ; Chromosomes, Human, Pair 1/genetics ; Chromosomes, Human, Pair 10/genetics ; Cohort Studies ; Dendritic Cells ; DNA Methylation ; Histology ; Mitosis ; Sequence Analysis, RNA ; Transcription Factors/genetics ; Gene Expression Regulation, Neoplastic/genetics
SCR Disease Name:
Teratoid Tumor, Atypical
Czasopismo naukowe
Tytuł:
Uncovering the phenotypic consequences of multi-locus imprinting disturbances using genome-wide methylation analysis in genomic imprinting disorders.
Autorzy:
Kim HY; Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, Seoul National University Bundang Hospital, Seongnam, Korea.
Shin CH; Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, Seoul National University College of Medicine, Seoul, Korea.
Shin CH; Department of Orthopaedics, Division of Pediatric Orthopedics, Seoul National University College of Medicine, Seoul, Korea.
Ko JM; Department of Pediatrics, Division of Clinical Genetics, Seoul National University College of Medicine, Seoul, Korea.; Rare Disease Center, Seoul National University Hospital, Seoul, Korea.
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Źródło:
PloS one [PLoS One] 2023 Aug 18; Vol. 18 (8), pp. e0290450. Date of Electronic Publication: 2023 Aug 18 (Print Publication: 2023).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genomic Imprinting*
DNA Methylation*
Humans ; Exome ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 6
Czasopismo naukowe
Tytuł:
Concomitant deletion of the short arm (del(1p13.3)) and amplification or gain (1q21) of chromosome 1 by fluorescence in situ hybridization are associated with a poor clinical outcome in multiple myeloma.
Autorzy:
Mohan M; Clinical Cancer Center, Division of Hematology Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Gong Z; Baylor Scott & White Charles A. Sammons Cancer Center, Houston, Texas, USA.
Ashby TC; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Al Hadidi S; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Thanendrarajan S; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Schinke C; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Alapat D; Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Shaughnessy JD Jr; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Zhan F; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
van Rhee F; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Sawyer JR; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Tian E; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Zangari M; Myeloma Center, Winthrop P. Rockefeller Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
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Źródło:
Cancer [Cancer] 2023 Aug 15; Vol. 129 (16), pp. 2491-2498. Date of Electronic Publication: 2023 Jun 06.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Multiple Myeloma*/therapy
Humans ; In Situ Hybridization, Fluorescence ; Chromosomes, Human, Pair 1/genetics ; Chromosome Aberrations ; Prognosis ; Chromosome Deletion
Czasopismo naukowe
Tytuł:
Characterization and Gene Mapping of an Open-Glume Oryza sativa L. Mutant.
Autorzy:
Mao X; Rice Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.; Guangdong Key Laboratory of New Technology in Rice Breeding, Guangzhou 510640, China.
Zheng X; Rice Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.; Guangdong Key Laboratory of New Technology in Rice Breeding, Guangzhou 510640, China.
Chen W; Rice Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.; Guangdong Key Laboratory of New Technology in Rice Breeding, Guangzhou 510640, China.
Li C; Rice Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.; Guangdong Key Laboratory of New Technology in Rice Breeding, Guangzhou 510640, China.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Aug 11; Vol. 24 (16). Date of Electronic Publication: 2023 Aug 11.
Typ publikacji:
Journal Article
MeSH Terms:
Oryza*/genetics
Humans ; Chromosome Mapping ; Agriculture ; Chromosomes, Human, Pair 1 ; Codon, Initiator
Czasopismo naukowe

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