Paper Review Records
All Paper Review Records
15 valid samples · Newest publication first
Review days = acceptance date − received date. PDF, DOI, and publisher-page sources are retained.
39
days
Establishment of a human induced pluripotent stem cell line, KMUGMCi011-A, from a patient bearing a frameshift mutation in the KMT2D gene leading Kabuki syndrome 1
Authors
Hiroki Ura; Takako Hiyoshi; Yo NiidaShow moreShow less
Affiliations
Center for Clinical Genomics, Kanazawa Medical University Hospital, 1-1 Daigaku, Uchinada, Kahoku, Ishikawa 920-0923, Japan; Division of Genomic Medicine, Department of Advanced Medicine, Medical Research Institute, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Kahoku, Ishikawa 920-0923, JapanShow moreShow less
44
days
Generation of high-quality reference control panels of human induced pluripotent stem cell clones from fibroblasts
Authors
Ellen Mosca; Elisabeth Stein; Jiss John; Manuela Kinzer; Maria Novatchkova; Harald Scheuch; Chukwuma Agu; Georg Stary; Josef M. Penninger; Arabella Meixner; Jennifer Volz-GlaserShow moreShow less
Affiliations
Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna BioCenter (VBC), Vienna, Austria; ABS Biotechnologies GmbH, Tulln, Austria; Department of Dermatology, Medical University of Vienna, Austria; Department of Laboratory Medicine, Medical University of Vienna, Austria; Helmholtz Centre for Infection Research, Braunschweig, Germany; Department of Medical Genetics, Life Science Institute, University of British Columbia, Vancouver, CanadaShow moreShow less
44
days
Generation of high-quality reference control panels of human induced pluripotent stem cell clones from PBMCs
Authors
Elisabeth Stein; Ellen Mosca; Jiss John; Manuela Kinzer; Maria Novatchkova; Harald Scheuch; Chukwuma Agu; Georg Stary; Josef M. Penninger; Arabella Meixner; Jennifer Volz-GlaserShow moreShow less
Affiliations
Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna BioCenter (VBC), Vienna, Austria; ABS Biotechnologies GmbH, Tulln, Austria; Department of Dermatology, Medical University of Vienna, Austria; Department of Laboratory Medicine, Medical University of Vienna, Austria; Helmholtz Centre for Infection Research, Braunschweig, Germany; Department of Medical Genetics, Life Science Institute, University of British Columbia, Vancouver, CanadaShow moreShow less
43
days
Two iPSC lines with frameshift mutations in FTSJ1 as models for X-linked non-syndromic intellectual disability
Authors
S. Edwards; J. Rhode; L. Hagenau; M.F. Hossain; T. Sura; A. Tzvetkova; B. Nowack; L.R. Jensen; A.W. KussShow moreShow less
Affiliations
Human Molecular Genetics Group, Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany; Institute of Bioinformatics, University Medicine Greifswald, Greifswald, Germany; SensID GmbH, Rostock, GermanyShow moreShow less
95
days
Generation of isogenic gene-corrected cell lines from a USH2A-RP patient-derived iPS cell line
Authors
Verónica Del Buey Furió; Belén García-Bohórquez; Gema García-García; M. Esther Gallardo; María José Gamundi; Zdenka Ellederova; Carmen Ayuso; José M. Millán; Slaven Erceg; Dunja LukovicShow moreShow less
Affiliations
Retinal Degeneration Lab, FCV Research Center Principe Felipe, Valencia, Spain; Molecular, Cellular, and Genomic Biomedicine Group, Health Research Institute La Fe, Valencia, Spain; Center for Biomedical Network Research On Rare Diseases (CIBERER), ISCIII, Madrid, Spain; Translational Research with iPS cells Group, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Madrid, Spain; Unitat de Genètica Molecular, Consorci Sanitari de Terrassa, Terrassa, Spain; Institute of Animal Physiology and Genetics, Czech Academy of Sciences, Libechov, Czech Republic; Department of Genetics, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain; Stem Cell Therapies in Neurodegenerative Diseases, Centro de Investigación Principe Felipe, Valencia, Spain; Retinal Degeneration Lab, Departamento Producción y Sanidad Animal, Salud Pública Veterinaria y Ciencia y Tecnología de los Alimentos, Facultad de Veterinaria, Universidad Cardenal Herrera-CEU, CEU Universities, Valencia, SpainShow moreShow less
55
days
Establishment of human induced pluripotent stem cell lines and isogenic gene-corrected controls from three patients with prolidase deficiency
Authors
Reecha Suri; Kevin Emmerich; Sahana Manohar-Sindhu; Elyse MacCall; Rebecca L Harper; Robin Schwartzbeck; Rebecca Huffstutler; Elisa Ferrante; Xuming Tang; Dan Yang; Natalia I Dmitrieva; Yongshun Lin; Jizhong Zou; Carlos R Ferreira; Ivona Aksentijevich; Alexandra F Freeman; Alessandra Brofferio; Cornelia Cudrici; Manfred BoehmShow moreShow less
Affiliations
Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA; College of Medicine, University of Kentucky, Lexington, KY 40536, USA; Cardiac Cellular Systems, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia; Centre for Cardiovascular Biology and Disease Research, La Trobe University, Victoria, Australia; Baker Department of Cardiometabolic Health, University of Melbourne, Victoria, Australia; Monash Alfred Baker Centre for Cardiovascular Research, Monash University, Victoria, Australia; Induced Pluripotent Stem Cells (iPSC) Core, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA; Unit on Skeletal Genomics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA; Inflammatory Disease Section, National Human Genome Research Institute, Bethesda, MD, USA; Laboratory of Clinical Immunology and Microbiology, NIAID, NIH, Bethesda, MD, USAShow moreShow less
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