-
1دورية أكاديمية
المؤلفون: Gjervan SC; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada., Ozgoren OK; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada., Gow A; Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI, United States., Stockler-Ipsiroglu S; Department of Pediatrics, The University of British Columbia and BC Children's Hospital, Vancouver, BC, Canada.; Division of Biochemical Genetics, The University of British Columbia and BC Children's Hospital, Vancouver, BC, Canada., Pouladi MA; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada.
المصدر: Frontiers in cellular neuroscience [Front Cell Neurosci] 2024 Jan 17; Vol. 17, pp. 1344090. Date of Electronic Publication: 2024 Jan 17 (Print Publication: 2023).
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101477935 Publication Model: eCollection Cited Medium: Print ISSN: 1662-5102 (Print) Linking ISSN: 16625102 NLM ISO Abbreviation: Front Cell Neurosci Subsets: PubMed not MEDLINE
-
2دورية أكاديمية
المؤلفون: Ozgoren OK; Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver V5Z 4H4, Canada; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada., Sequiera GL; Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver V5Z 4H4, Canada; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada., Ferrari Bardile C; Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver V5Z 4H4, Canada; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada., Gjervan SC; Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver V5Z 4H4, Canada; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada., Salman A; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada., Lehman A; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada., Turvey SE; Department of Pediatrics, The University of British Columbia and BC Children's Hospital, Vancouver, British Columbia, Canada., Ross CJD; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada., Stockler S; Department of Pediatrics, The University of British Columbia and BC Children's Hospital, Vancouver, British Columbia, Canada., Pouladi MA; Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver V5Z 4H4, Canada; Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada. Electronic address: map@pouladilab.org.
المصدر: Stem cell research [Stem Cell Res] 2023 Sep; Vol. 71, pp. 103174. Date of Electronic Publication: 2023 Jul 28.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Elsevier Country of Publication: England NLM ID: 101316957 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1876-7753 (Electronic) Linking ISSN: 18735061 NLM ISO Abbreviation: Stem Cell Res Subsets: MEDLINE
مواضيع طبية MeSH: Hereditary Central Nervous System Demyelinating Diseases*/genetics , Hereditary Central Nervous System Demyelinating Diseases*/pathology , Pluripotent Stem Cells*/pathology , Cell Line*, Humans ; Male ; Child ; Fibroblasts/pathology
SCR Disease Name: Leukodystrophy, Hypomyelinating, 2