Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kalaskar VK"'
Autor:
Boobalan E; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Thompson AH; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Alur RP; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., McGaughey DM; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Dong L; Mouse Genetic Engineering Core, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Shih G; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Vieta-Ferrer ER; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Onojafe IF; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Kalaskar VK; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Arno G; University College London Institute of Ophthalmology, London, United Kingdom.; Moorfields Eye Hospital, London, United Kingdom., Lotery AJ; Faculty of Medicine, University of Southampton, Southampton, United Kingdom., Guan B; Ophthalmic Genetics Laboratory, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Bender C; Ophthalmic Genetics Laboratory, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Memon O; Ocular and Stem Cell Translational Research Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Brinster L; Division of Veterinary Resources, Office of Research Services, National Institutes of Health, Bethesda, Maryland, United States., Soleilhavoup C; MRC Toxicology Unit, University of Cambridge, Leicester, United Kingdom., Panman L; MRC Toxicology Unit, University of Cambridge, Leicester, United Kingdom., Badea TC; Retinal Circuit Development and Genetics Unit, Neurobiology, Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States.; Research and Development Institute, Transilvania University of Brașov, Brașov, Romania.; National Center for Brain Research, ICIA, Romanian Academy, Bucharest, România., Minella A; Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, California, United States., Lopez AJ; Department of Ophthalmology and Vision Science, School of Medicine, University of California-Davis, Davis, California, United States., Thomasy SM; Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, California, United States.; Department of Ophthalmology and Vision Science, School of Medicine, University of California-Davis, Davis, California, United States., Moshiri A; Department of Ophthalmology and Vision Science, School of Medicine, University of California-Davis, Davis, California, United States., Blain D; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Hufnagel RB; Ophthalmic Genetics Laboratory, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Cogliati T; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Bharti K; Ocular and Stem Cell Translational Research Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States., Brooks BP; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics & Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, United States.
Publikováno v:
Investigative ophthalmology & visual science [Invest Ophthalmol Vis Sci] 2022 Nov 01; Vol. 63 (12), pp. 5.
Autor:
Kalaskar VK; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics and Visual Function Branch (OGVFB), National Eye Institute (NEI), National Institutes of Health (NIH), Bethesda, Maryland., Alur RP; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics and Visual Function Branch (OGVFB), National Eye Institute (NEI), National Institutes of Health (NIH), Bethesda, Maryland., Li LK; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics and Visual Function Branch (OGVFB), National Eye Institute (NEI), National Institutes of Health (NIH), Bethesda, Maryland., Thomas JW; National Institutes of Health Intramural Sequencing Center, National Human Genome Research Institute, NIH, Bethesda, Maryland., Sergeev YV; Protein Biochemistry and Molecular Modeling Group, OGVFB, NEI, NIH, Bethesda, Maryland., Blain D; Ophthalmic Clinical Genetics Section, OGVFB, NEI, NIH, Bethesda, Maryland., Hufnagel RB; Medical Genetics and Ophthalmic Genomics Unit, OGVFB, NEI, NIH, Bethesda, Maryland., Cogliati T; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics and Visual Function Branch (OGVFB), National Eye Institute (NEI), National Institutes of Health (NIH), Bethesda, Maryland., Brooks BP; Pediatric, Developmental & Genetic Ophthalmology Section, Ophthalmic Genetics and Visual Function Branch (OGVFB), National Eye Institute (NEI), National Institutes of Health (NIH), Bethesda, Maryland.; Ophthalmic Clinical Genetics Section, OGVFB, NEI, NIH, Bethesda, Maryland.
Publikováno v:
Human mutation [Hum Mutat] 2020 Mar; Vol. 41 (3), pp. 678-695. Date of Electronic Publication: 2019 Dec 09.
Autor:
Kalaskar VK; Neuroscience Division of the Biomedical & Health Sciences Institute, University of Georgia., Lauderdale JD; Neuroscience Division of the Biomedical & Health Sciences Institute, University of Georgia; Department of Cellular Biology, University of Georgia; jdlauder@uga.edu.
Publikováno v:
Journal of visualized experiments : JoVE [J Vis Exp] 2014 Mar 01 (85). Date of Electronic Publication: 2014 Mar 01.
Autor:
DeYoung, Charles1 (AUTHOR), Guan, Bin1 (AUTHOR), Ullah, Ehsan1 (AUTHOR), Blain, Delphine1 (AUTHOR), Hufnagel, Robert B.1 (AUTHOR), Brooks, Brian P.1 (AUTHOR) brooksb@nei.nih.gov
Publikováno v:
Ophthalmic Genetics. Aug2022, Vol. 43 Issue 4, p513-517. 5p.
Autor:
Xue Dong, Landford, Wilmina N., Hart, James, Risolino, Maurizio, Kaymakcalan, Omer, Jin, Julia, Toyoda, Yoshiko, Ferretti, Elisabetta, Selleri, Licia, Spector, Jason A.
Publikováno v:
Plastic & Reconstructive Surgery; Jul2017, Vol. 140 Issue 1, p75-85, 11p
Autor:
Barry, David M., Yeon Koo, Norden, Pieter R., Wylie, Lyndsay A., Ke Xu, Wichaidit, Chonlarat, Azizoglu, D. Berfin, Yi Zheng, Cobb, Melanie H., Davis, George E., Cleaver, Ondine
Publikováno v:
Circulation Research; 9/16/2016, Vol. 119 Issue 7, p810-826, 17p
Autor:
Aubert-Mucca M; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France., Pernin-Grandjean J; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France., Marchasson S; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France., Gaston V; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France., Habib C; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France., Meunier I; Centre de Référence des Maladies Sensorielles Génétiques, Hôpital Gui de Chauliac, Institut de Neurosciences de Montpellier, INSERM U1051, Université de Montpellier, Montpellier, France., Sigaudy S; Département de Génétique Médicale, AP-HM, CHU Timone Enfants, Marseille, France., Kaplan J; Laboratoire de Génétique Ophtalmologique, INSERM U1163 Institut Imagine, Paris, France., Roche O; Département d'Ophtalmologie, IHU Necker-Enfants-Malades, Université Paris-Descartes, Paris, France., Denis D; Institut de Neurosciences de la Timone (INT), Centre National de la Recherche Scientifique (CNRS), Aix-Marseille Université (AMU), Marseille, France., Bitoun P; Département d'Ophtalmologie, SIDVA 91, Juvisy-sur-Orge, France., Haye D; Département de Génétique, Hôpital Robert Debré, Paris, France., Verloes A; Département de Génétique, Hôpital Robert Debré, Paris, France., Calvas P; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.; INSERM U1056, UDEAR, Equipe 4, Université Toulouse III, Toulouse, France.; Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, CHU Toulouse, Toulouse, France., Chassaing N; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.; INSERM U1056, UDEAR, Equipe 4, Université Toulouse III, Toulouse, France.; Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, CHU Toulouse, Toulouse, France., Plaisancié J; Service de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France. plaisancie.j@chu-toulouse.fr.; INSERM U1056, UDEAR, Equipe 4, Université Toulouse III, Toulouse, France. plaisancie.j@chu-toulouse.fr.; Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, CHU Toulouse, Toulouse, France. plaisancie.j@chu-toulouse.fr.
Publikováno v:
European journal of human genetics : EJHG [Eur J Hum Genet] 2021 Jan; Vol. 29 (1), pp. 131-140. Date of Electronic Publication: 2020 Jul 31.
For decades, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics has served as the ultimate resource for clinicians integrating genetics and genomics into medical practice. With detailed coverage in contributions from more tha
