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Investigative Ophthalmology & Visual Science|June 7, 2011
Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genesJianjun Chen, Nizar Smaoui, Monia Ben Hamed Hammer, et al.
Zoological Research|January 6, 2026
<i>ARR3</i> variant-induced cone mosaicism alters cone subtype composition and disrupts phototransductionJiamin Ouyang, Zhen Yi, Yi Jiang, et al.
The Journal of Physical Chemistry. B|May 14, 2019
Photochemical Spin Dynamics of the Vitamin B<sub>12</sub> Derivative, MethylcobalaminValentina Lukinović, Jonathan R Woodward, Teresa C Marrafa, et al.
Human Genetics|July 11, 2002
Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophyZhaoxia Ren, Pei-Yu Lin, Gordon K Klintworth, et al.
American Journal of Preventive Medicine|May 12, 2000
Methods for systematic reviews of economic evaluations for the Guide to Community Preventive Services. Task Force on Community Preventive ServicesV G Carande-Kulis, M V Maciosek, P A Briss, et al.
American Journal of Human Genetics|August 28, 2010
A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosaLin Li, Naoki Nakaya, Venkata R M Chavali, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 2026
DAPL1 restrains RPE PANoptosis in experimental AMD by inhibiting GRP75-mediated mitochondria-associated endoplasmic reticulum membranesYan Li, Meiyu Jing, Wanxiao Wang, et al.
Human Genome Variation|May 16, 2020
Mutations in <i>CERKL</i> and <i>RP1</i> cause retinitis pigmentosa in Pakistani familiesRaheela Nadeem, Firoz Kabir, Jiali Li, et al.
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