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Wyszukujesz frazę ""Cadherin"" wg kryterium: Temat


Tytuł:
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes.
Autorzy:
Hitti-Malin RJ; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands.
Panneman DM; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands.
Corradi Z; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands.
Boonen EGM; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands.
Astuti G; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands.
Dhaenens CM; Univ. Lille, Inserm, CHU Lille, U1172-LilNCog-Lille Neuroscience & Cognition, F-59000 Lille, France.
Stöhr H; Institute of Human Genetics, University of Regensburg, 93053 Regensburg, Germany.
Weber BHF; Institute of Human Genetics, University of Regensburg, 93053 Regensburg, Germany.; Institute of Clinical Human Genetics, University Hospital Regensburg, 93053 Regensburg, Germany.
Sharon D; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 91120, Israel.
Banin E; Department of Ophthalmology, Hadassah Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 91120, Israel.
Karali M; Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.; Eye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania 'Luigi Vanvitelli', 80131 Naples, Italy.
Banfi S; Department of Precision Medicine, University of Campania 'Luigi Vanvitelli', 80138 Naples, Italy.; Eye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, University of Campania 'Luigi Vanvitelli', 80131 Naples, Italy.; Telethon Institute of Genetics and Medicine (TIGEM), 80078 Pozzuoli, Italy.
Ben-Yosef T; Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 31096, Israel.
Glavač D; Department of Molecular Genetics, Institute of Pathology, Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.; Center for Human Genetics and Pharmacogenomics, Faculty of Medicine, University of Maribor, 2000 Maribor, Slovenia.
Farrar GJ; The School of Genetics and Microbiology, The University of Dublin Trinity College, D02 VF25 Dublin, Ireland.
Ayuso C; Department of Genetics, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28049 Madrid, Spain.; Center for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Liskova P; Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 08 Prague, Czech Republic.; Department of Ophthalmology, First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 08 Prague, Czech Republic.
Dudakova L; Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 08 Prague, Czech Republic.
Vajter M; Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 08 Prague, Czech Republic.; Department of Ophthalmology, First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 08 Prague, Czech Republic.
Ołdak M; Department of Histology and Embryology, Medical University of Warsaw, 02-004 Warsaw, Poland.
Szaflik JP; Department of Ophthalmology, Medical University of Warsaw, SPKSO Ophthalmic University Hospital, 03-709 Warsaw, Poland.
Matynia A; College of Optometry, University of Houston, Houston, TX 77004, USA.; Jules Stein Eye Institute, Los Angeles, CA 90095, USA.; Ophthalmology, University of California Los Angeles David Geffen School of Medicine, Los Angeles, CA 90095, USA.
Gorin MB; Jules Stein Eye Institute, Los Angeles, CA 90095, USA.
Kämpjärvi K; Blueprint Genetics, 02150 Espoo, Finland.
Bauwens M; Department of Biomolecular Medicine, Ghent University, 9000 Ghent, Belgium.; Center for Medical Genetics, Ghent University Hospital, 9000 Ghent, Belgium.
De Baere E; Department of Biomolecular Medicine, Ghent University, 9000 Ghent, Belgium.; Center for Medical Genetics, Ghent University Hospital, 9000 Ghent, Belgium.
Hoyng CB; Department of Ophthalmology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Li CHZ; Department of Ophthalmology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Klaver CCW; Department of Ophthalmology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Inglehearn CF; Division of Molecular Medicine, Leeds Institute of Medical Research, St. James's University Hospital, University of Leeds, Leeds LS9 7TF, UK.
Fujinami K; Department of Ophthalmology, The Jikei University School of Medicine, Tokyo 105-8461, Japan.
Rivolta C; Institute of Molecular and Clinical Ophthalmology Basel, 4031 Basel, Switzerland.
Allikmets R; Department of Ophthalmology, Columbia University, New York, NY 10027, USA.; Department of Pathology & Cell Biology, Columbia University, New York, NY 10027, USA.
Zernant J; Department of Ophthalmology, Columbia University, New York, NY 10027, USA.
Lee W; Department of Ophthalmology, Columbia University, New York, NY 10027, USA.
Podhajcer OL; Laboratorio de Terapia Molecular y Celular (Genocan), Fundación Instituto Leloir, CONICET, Buenos Aires 1405, Argentina.
Fakin A; Eye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.; Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.
Sajovic J; Eye Hospital, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.; Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.
AlTalbishi A; St John of Jerusalem Eye Hospital Group, East Jerusalem 91198, Palestine.
Valeina S; Department of Ophthalmology, Riga Stradins University, LV-1007 Riga, Latvia.; Children's Clinical University Hospital, LV-1004 Riga, Latvia.
Taurina G; Children's Clinical University Hospital, LV-1004 Riga, Latvia.
Vincent AL; Department of Ophthalmology, New Zealand National Eye Centre, Faculty of Medical and Health Sciences, The University of Auckland, Grafton, Auckland 1023, New Zealand.; Eye Department, Greenlane Clinical Centre, Auckland District Health Board, Auckland 1142, New Zealand.
Roberts L; University of Cape Town/MRC Precision and Genomic Medicine Research Unit, Division of Human Genetics, Department of Pathology, Institute of Infectious Disease and Molecular Medicine (IDM), Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.
Ramesar R; University of Cape Town/MRC Precision and Genomic Medicine Research Unit, Division of Human Genetics, Department of Pathology, Institute of Infectious Disease and Molecular Medicine (IDM), Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa.
Sartor G; Department of Pharmacy and Biotechnology, University of Bologna, 40127 Bologna, Italy.
Luppi E; Department of Medical and Surgical Sciences, University of Bologna, 40127 Bologna, Italy.; Unit of Medical Genetics, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Downes SM; Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, Oxford University, Oxford OX3 9DU, UK.; Oxford Eye Hospital, Oxford University NHS Foundation Trust, Oxford OX3 9DU, UK.
van den Born LI; The Rotterdam Eye Hospital, 3011 BH Rotterdam, The Netherlands.
McLaren TL; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, WA 6009, Australia.; Centre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, WA 6009, Australia.
De Roach JN; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, WA 6009, Australia.; Centre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, WA 6009, Australia.
Lamey TM; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, WA 6009, Australia.; Centre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, WA 6009, Australia.
Thompson JA; Australian Inherited Retinal Disease Registry and DNA Bank, Department of Medical Technology and Physics, Sir Charles Gairdner Hospital, Nedlands, WA 6009, Australia.
Chen FK; Centre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, WA 6009, Australia.
Tracewska AM; Datana Solutions, 54-530 Wroclaw, Poland.
Kamakari S; Ophthalmic Genetics Unit, OMMA Ophthalmological Institute of Athens, 115 25 Athens, Greece.
Sallum JMF; Department of Ophthalmology and Visual Sciences, Universidade Federal de São Paulo, São Paulo 04023-062, SP, Brazil.; Instituto de Genética Ocular, São Paulo 04552-050, SP, Brazil.
Bolz HJ; Institute of Human Genetics, University Hospital of Cologne, 50937 Cologne, Germany.
Kayserili H; Department of Medical Genetics, Koc University School of Medicine (KUSOM), 34450 Istanbul, Turkey.
Roosing S; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands.
Cremers FPM; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands.
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Źródło:
Biomolecules [Biomolecules] 2024 Mar 19; Vol. 14 (3). Date of Electronic Publication: 2024 Mar 19.
Typ publikacji:
Journal Article
MeSH Terms:
Macular Degeneration*/genetics
Humans ; Mutation ; Penetrance ; Pedigree ; Retina ; Phenotype ; ATP-Binding Cassette Transporters/genetics ; Eye Proteins ; Cadherin Related Proteins ; Nerve Tissue Proteins/genetics
Czasopismo naukowe
Tytuł:
Protocadherin Gamma C3 (PCDHGC3) Is Strongly Expressed in Glioblastoma and Its High Expression Is Associated with Longer Progression-Free Survival of Patients.
Autorzy:
Feldheim J; Section Experimental Neurosurgery, Department of Neurosurgery, University Hospital Würzburg, 97080 Würzburg, Germany.; Center for Translational Neuro- and Behavioral Sciences, University Hospital Essen, 45147 Essen, Germany.; Division of Clinical Neurooncology, Department of Neurology, University Hospital Essen, 45147 Essen, Germany.
Wend D; Section Experimental Neurosurgery, Department of Neurosurgery, University Hospital Würzburg, 97080 Würzburg, Germany.; Department of Anaesthesiology, Intensive Care, Emergency and Pain Medicine, University Hospital Würzburg, 97080 Würzburg, Germany.
Lauer MJ; Department of Anaesthesiology, Intensive Care, Emergency and Pain Medicine, University Hospital Würzburg, 97080 Würzburg, Germany.; Graduate School of Life Sciences, Julius-Maximilians-University Würzburg, 97074 Würzburg, Germany.
Monoranu CM; Department of Neuropathology, Institute of Pathology, Julius-Maximilians-University Würzburg, 97080 Würzburg, Germany.
Glas M; Center for Translational Neuro- and Behavioral Sciences, University Hospital Essen, 45147 Essen, Germany.; Division of Clinical Neurooncology, Department of Neurology, University Hospital Essen, 45147 Essen, Germany.
Kleinschnitz C; Center for Translational Neuro- and Behavioral Sciences, University Hospital Essen, 45147 Essen, Germany.; Division of Clinical Neurooncology, Department of Neurology, University Hospital Essen, 45147 Essen, Germany.
Ernestus RI; Section Experimental Neurosurgery, Department of Neurosurgery, University Hospital Würzburg, 97080 Würzburg, Germany.
Braunger BM; Institute of Anatomy and Cell Biology, Julius-Maximilians-University Würzburg, 97070 Würzburg, Germany.
Meybohm P; Department of Anaesthesiology, Intensive Care, Emergency and Pain Medicine, University Hospital Würzburg, 97080 Würzburg, Germany.
Hagemann C; Section Experimental Neurosurgery, Department of Neurosurgery, University Hospital Würzburg, 97080 Würzburg, Germany.
Burek M; Department of Anaesthesiology, Intensive Care, Emergency and Pain Medicine, University Hospital Würzburg, 97080 Würzburg, Germany.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Jul 22; Vol. 23 (15). Date of Electronic Publication: 2022 Jul 22.
Typ publikacji:
Journal Article
MeSH Terms:
Brain Neoplasms*/genetics
Cadherin Related Proteins*/genetics
Glioblastoma*/genetics
Glioma*/genetics
Cadherins/genetics ; Cadherins/metabolism ; Humans ; Progression-Free Survival ; Protocadherins ; RNA, Messenger
Czasopismo naukowe
Tytuł:
Heterophilic and homophilic cadherin interactions in intestinal intermicrovillar links are species dependent.
Autorzy:
Gray ME; Ohio State Biochemistry Program, The Ohio State University, Columbus, Ohio, United States of America.; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio, United States of America.
Johnson ZR; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio, United States of America.
Modak D; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio, United States of America.
Tamilselvan E; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio, United States of America.; Biophysics Program, The Ohio State University, Columbus, Ohio, United States of America.
Tyska MJ; Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
Sotomayor M; Ohio State Biochemistry Program, The Ohio State University, Columbus, Ohio, United States of America.; Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio, United States of America.; Biophysics Program, The Ohio State University, Columbus, Ohio, United States of America.
Pokaż więcej
Źródło:
PLoS biology [PLoS Biol] 2021 Dec 06; Vol. 19 (12), pp. e3001463. Date of Electronic Publication: 2021 Dec 06 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Cadherin Related Proteins/*ultrastructure
Microvilli/*pathology
Animals ; Caco-2 Cells ; Cadherin Related Proteins/metabolism ; Cadherins/metabolism ; Carrier Proteins/metabolism ; Cell Adhesion ; Cell Adhesion Molecules/metabolism ; Cell Communication ; Cell Line ; Enterocytes/metabolism ; Enterocytes/physiology ; Epithelial Cells/metabolism ; Humans ; Intestine, Small/pathology ; Intestine, Small/physiology ; Mice ; Microvilli/physiology ; Species Specificity
Czasopismo naukowe
Tytuł:
Panel-based next-generation sequencing identifies novel mutations in Bulgarian patients with inherited retinal dystrophies.
Autorzy:
Kamenarova K; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.; Laboratory of Genomic Diagnostics, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.
Mihova K; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.; Laboratory of Genomic Diagnostics, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.
Veleva N; Department of Ophthalmology, University Hospital 'Alexandrovska', Medical University of Sofia, Sofia, Bulgaria.
Mermeklieva E; Clinic of Ophthalmology, University Hospital 'Lozenetz', Medical Faculty, Sofia University 'St. Kliment Ohridski', Sofia, Bulgaria.
Mihaylova B; Clinic 'Vision', Sofia, Bulgaria.
Dimitrova G; Department of Ophthalmology, University Hospital 'Alexandrovska', Medical University of Sofia, Sofia, Bulgaria.
Oscar A; Department of Ophthalmology, University Hospital 'Alexandrovska', Medical University of Sofia, Sofia, Bulgaria.
Shandurkov I; Clinic 'Vision', Sofia, Bulgaria.
Cherninkova S; Department of Neurology, University hospital 'Alexandrovska', Medical University of Sofia, Sofia, Bulgaria.
Kaneva R; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.; Laboratory of Genomic Diagnostics, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2022 Aug; Vol. 10 (8), pp. e1997. Date of Electronic Publication: 2022 Jun 03.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
DNA Copy Number Variations*
Retinal Dystrophies*/diagnosis
Retinal Dystrophies*/genetics
ATP-Binding Cassette Transporters/genetics ; Bestrophins/genetics ; Bulgaria ; Cadherin Related Proteins ; Cadherins/genetics ; Eye Proteins/genetics ; High-Throughput Nucleotide Sequencing ; Humans ; Mutation ; Nerve Tissue Proteins/genetics ; Pedigree
Czasopismo naukowe
Tytuł:
The Impact of Transcriptional Profiling Cadherin Family and Therapeutic Approaches of Gastric Cancer: A Translational Outlook on Multi-omics Data Analysis
Autorzy:
Wang, Huan
Zhang, BaominAff2, IDs12010024049262_cor2
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Źródło:
Applied Biochemistry and Biotechnology. :1-18
Czasopismo naukowe
Tytuł:
Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways.
Autorzy:
Zhen Y; Menzies Institute for Medical Research, University of Tasmania, Liverpool St, Hobart, 7000, Australia.
Cullen CL; Menzies Institute for Medical Research, University of Tasmania, Liverpool St, Hobart, 7000, Australia.
Ricci R; Menzies Institute for Medical Research, University of Tasmania, Liverpool St, Hobart, 7000, Australia.
Summers BS; Menzies Institute for Medical Research, University of Tasmania, Liverpool St, Hobart, 7000, Australia.
Rehman S; Department of Otorhinolaryngology Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, MD, 21201, USA.
Ahmed ZM; Department of Otorhinolaryngology Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, MD, 21201, USA.
Foster AY; Jungers Center for Neurosciences Research, Department of Neurology, Oregon Health & Science University, Portland, OR, 97239, USA.
Emery B; Jungers Center for Neurosciences Research, Department of Neurology, Oregon Health & Science University, Portland, OR, 97239, USA.
Gasperini R; Menzies Institute for Medical Research, University of Tasmania, Liverpool St, Hobart, 7000, Australia.; School of Medicine, University of Tasmania, Liverpool St, Hobart, 7000, Australia.
Young KM; Menzies Institute for Medical Research, University of Tasmania, Liverpool St, Hobart, 7000, Australia. .
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Źródło:
Communications biology [Commun Biol] 2022 May 30; Vol. 5 (1), pp. 511. Date of Electronic Publication: 2022 May 30.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:
Glioma*/genetics
Glioma*/metabolism
Oligodendrocyte Precursor Cells*
Cadherin Related Proteins ; Cell Proliferation ; Humans ; Oligodendroglia ; Protocadherins
Czasopismo naukowe
Tytuł:
Role of CDH23 as a prognostic biomarker and its relationship with immune infiltration in acute myeloid leukemia.
Autorzy:
Yang J; Department of Hematology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Lu F; Department of Hematology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Ma G; Hematology and Oncology Unit, Department of Geriatrics, Qilu Hospital of Shandong University, Jinan, China.
Pang Y; Department of Hematology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Zhao Y; Department of Hematology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Sun T; Department of Hematology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Ma D; Department of Hematology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Ye J; Department of Hematology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Ji C; Department of Hematology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China. .
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Źródło:
BMC cancer [BMC Cancer] 2022 May 21; Vol. 22 (1), pp. 568. Date of Electronic Publication: 2022 May 21.
Typ publikacji:
Journal Article
MeSH Terms:
Leukemia, Myeloid, Acute*/pathology
Biomarkers ; Cadherin Related Proteins ; Cadherins/genetics ; Gene Expression Profiling ; Humans ; Prognosis
Czasopismo naukowe
Tytuł:
Association between genetic polymorphisms of cadherin 23 and noise-induced hearing loss: a meta-analysis.
Autorzy:
Wu ZD; Guangdong Provincial Engineering Research Center of Public Health Detection and Assessment, School of Public Health, Guangdong Pharmaceutical University, Guangzhou, China.
Lu JQ; Yuexiu District Center for Disease Control and Prevention, Guangzhou, China.
Du WJ; Guangdong Provincial Engineering Research Center of Public Health Detection and Assessment, School of Public Health, Guangdong Pharmaceutical University, Guangzhou, China.
Wu S; Guangdong Provincial Engineering Research Center of Public Health Detection and Assessment, School of Public Health, Guangdong Pharmaceutical University, Guangzhou, China.
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Źródło:
Annals of human biology [Ann Hum Biol] 2022 Feb; Vol. 49 (1), pp. 41-53.
Typ publikacji:
Journal Article; Meta-Analysis
MeSH Terms:
Hearing Loss, Noise-Induced*/genetics
Asian People ; Cadherin Related Proteins ; Cadherins/genetics ; Genetic Predisposition to Disease ; Humans ; Polymorphism, Genetic
Czasopismo naukowe
Tytuł:
Leaf Extract from European Olive (Olea europaea L.) Post-Transcriptionally Suppresses the Epithelial-Mesenchymal Transition and Sensitizes Gastric Cancer Cells to Chemotherapy
Autorzy:
Tekin, Cagla
Ercelik, Melis
Dunaev, Pavel
Galembikova, Aigul
Tezcan, Gulcin
Aksoy, Secil AkAff4, Aff5
Budak, Ferah
Isık, Ozgen
Ugras, Nesrin
Boichuk, SergeiAff2, Aff9, Aff10, IDS0006297924010061_cor10
Tunca, BerrinAff1, IDS0006297924010061_cor11
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Źródło:
Biochemistry (Moscow). 89(1):97-115
Czasopismo naukowe
Tytuł:
Vascular senescence and leak are features of the early breakdown of the blood–brain barrier in Alzheimer’s disease models
Autorzy:
Ting, Ka KaAff1, Aff5, IDs1135702300927x_cor1
Coleman, PaulAff1, Aff5
Kim, Hani Jieun
Zhao, Yang
Mulangala, Jocelyne
Cheng, Ngan Ching
Li, Wan
Gunatilake, Dilini
Johnstone, Daniel M.Aff5, Aff6
Loo, Lipin
Neely, G. Gregory
Yang, Pengyi
Götz, Jürgen
Vadas, Mathew A.Aff1, Aff9
Gamble, Jennifer R.Aff1, Aff5, IDs1135702300927x_cor15
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Źródło:
GeroScience: Official Journal of the American Aging Association (AGE). 45(6):3307-3331
Czasopismo naukowe
Tytuł:
The GSDMB rs7216389 SNP is associated with chronic rhinosinusitis in a multi-institutional cohort.
Autorzy:
Zack DE; Department of Otolaryngology, University of Arizona, Tucson, Arizona, USA.
Stern DA; Asthma and Airway Disease Research Center, University of Arizona, Tucson, Arizona, USA.
Willis AL; Department of Otolaryngology, University of Arizona, Tucson, Arizona, USA.
Kim AS; Department of Otolaryngology, University of Arizona, Tucson, Arizona, USA.
Mansfield CJ; Department of Otorhinolaryngology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Reed DR; Monell Chemical Senses Center, Philadelphia, Pennsylvania, USA.
Brooks SG; Department of Otorhinolaryngology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Adappa ND; Department of Otorhinolaryngology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Palmer JN; Department of Otorhinolaryngology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Cohen NA; Department of Otorhinolaryngology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Monell Chemical Senses Center, Philadelphia, Pennsylvania, USA.
Chiu AG; Department of Otolaryngology, University of Kansas Medical Center, Kansas City, Kansas, USA.
Song BH; Department of Otolaryngology, University of Arizona, Tucson, Arizona, USA.
Le CH; Department of Otolaryngology, University of Arizona, Tucson, Arizona, USA.
Chang EH; Department of Otolaryngology, University of Arizona, Tucson, Arizona, USA.
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Źródło:
International forum of allergy & rhinology [Int Forum Allergy Rhinol] 2021 Dec; Vol. 11 (12), pp. 1647-1653. Date of Electronic Publication: 2021 Jun 02.
Typ publikacji:
Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural
MeSH Terms:
Genetic Predisposition to Disease*
Polymorphism, Single Nucleotide*
Neoplasm Proteins/*genetics
Sinusitis/*genetics
Adult ; Cadherin Related Proteins ; Cadherins/genetics ; Case-Control Studies ; Child ; Chronic Disease ; Genotype ; Humans ; Membrane Proteins/genetics ; Retrospective Studies
Czasopismo naukowe
Tytuł:
A rare case of RGR/CDHR1 haplotype identified in Bulgarian patient with cone-rod dystrophy.
Autorzy:
Mermeklieva E; Clinic of Оphthalmology, 'Lozenetz' University Hospital, Medical Faculty, Sofia University 'St. Kliment Ohridski', Sofia, Bulgaria.
Kamenarova K; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University - Sofia, Sofia, Bulgaria.
Mihova K; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University - Sofia, Sofia, Bulgaria.
Shakola F; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University - Sofia, Sofia, Bulgaria.
Kaneva R; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University - Sofia, Sofia, Bulgaria.
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Źródło:
Ophthalmic genetics [Ophthalmic Genet] 2021 Dec; Vol. 42 (6), pp. 747-752. Date of Electronic Publication: 2021 Jul 06.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cadherin Related Proteins/*genetics
Cone-Rod Dystrophies/*genetics
Eye Proteins/*genetics
Haplotypes/*genetics
Mutation/*genetics
Nerve Tissue Proteins/*genetics
Receptors, G-Protein-Coupled/*genetics
Adult ; Bulgaria/epidemiology ; Cone-Rod Dystrophies/diagnostic imaging ; Cone-Rod Dystrophies/epidemiology ; Cone-Rod Dystrophies/physiopathology ; DNA Mutational Analysis ; Electroretinography ; Female ; Fluorescein Angiography ; High-Throughput Nucleotide Sequencing ; Humans ; Pedigree ; Retina/physiopathology ; Tomography, Optical Coherence ; Visual Acuity/physiology ; Visual Field Tests ; Visual Fields/physiology
Czasopismo naukowe

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