Результати пошуку - Minzhong Yu
- Показ 1 - 10 результатів із 10
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The Role of Visual Electrophysiology in Systemic Hereditary Syndromes за авторством Minzhong Yu, Emile R. Vieta-Ferrer, Anas Bakdalieh, T. H. Tsai
Опубліковано 2025Revisão -
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A Novel Role of Complement in Retinal Degeneration за авторством Minzhong Yu, Weilin Zou, Neal S. Peachey, Thomas M. McIntyre, Jinbo Liu
Опубліковано 2012Artigo -
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Genetic loss of function of Ptbp1 does not induce glia-to-neuron conversion in retina за авторством Thanh Hoang, Dong Won Kim, Haley Appel, Nicole Pannullo, Patrick J. Leavey, Manabu Ozawa, Sika Zheng, Minzhong Yu, Neal S. Peachey, Seth Blackshaw
Опубліковано 2022Artigo -
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Mouse models of human ocular disease for translational research за авторством Mark P. Krebs, Gayle B. Collin, Wanda L. Hicks, Minzhong Yu, Jeremy R. Charette, Lan Ying Shi, Jieping Wang, Jürgen Κ. Naggert, Neal S. Peachey, Patsy M. Nishina
Опубліковано 2017Artigo -
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Disruption of murine<i>Adamtsl4</i>results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation за авторством Gayle B. Collin, Dirk Hubmacher, Jeremy R. Charette, Wanda L. Hicks, Lisa Stone, Minzhong Yu, Jürgen Κ. Naggert, Mark P. Krebs, Neal S. Peachey, Suneel Apte, Patsy M. Nishina
Опубліковано 2015Artigo -
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Glucose uptake by <scp>GLUT1</scp> in photoreceptors is essential for outer segment renewal and rod photoreceptor survival за авторством Lauren L. Daniele, John Y.S. Han, Ivy S. Samuels, Ravikiran Komirisetty, Nikhil Mehta, Jessica L. McCord, Minzhong Yu, Yekai Wang, Kathleen Boesze‐Battaglia, Brent A. Bell, Jianhai Du, Neal S. Peachey, Nancy J. Philp
Опубліковано 2022Artigo -
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Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity за авторством Nicole T.M. Saksens, Mark P. Krebs, Frederieke E. Schoenmaker-Koller, Wanda L. Hicks, Minzhong Yu, Lan-Ying Shi, Lucy B. Rowe, Gayle B. Collin, Jeremy R. Charette, Stef J.F. Letteboer, Kornelia Neveling, Tamara W van Moorsel, Sleiman Abu-Ltaif, Elfride De Baere, Sophie Walraedt, Sandro Banfi, Francesca Simonelli, Frans P.M. Cremers, Camiel J.F. Boon, Ronald Roepman, Bart P. Leroy, Neal S. Peachey, Carel B. Hoyng, Patsy M. Nishina, Anneke I. den Hollander
Опубліковано 2015Artigo
Інструменти для пошуку:
Пов'язані теми
Biology
Cell biology
Gene
Neuroscience
Biochemistry
Genetics
Retina
Medicine
Retinal
Phenotype
Retinal degeneration
Retinal pigment epithelium
Disease
Electroretinography
Ophthalmology
Pathology
Apoptosis
Paleontology
Photoreceptor cell
Programmed cell death
Retinitis pigmentosa
ADAMTS
Achromatopsia
Allele
Alternative complement pathway
Angiogenesis
Antioxidant
Artificial intelligence
Ataxia
Bardet–Biedl syndrome