Torthaí cuardaigh - Bassuk, Alexander G
- 1 - 20 toradh as 117 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Response to Sandford et al.: PRICKLE2 Variants in Epilepsy: A Call for Precision Medicine de réir Mahajan, Vinit B., Bassuk, Alexander G.
Foilsithe / Cruthaithe 2016Téacs -
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A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyria de réir Bassuk, Alexander G., Sherr, Elliott H.
Foilsithe / Cruthaithe 2016Téacs -
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Prickle1 stunts limb growth through alteration of cell polarity and gene expression de réir Yang, Tian, Bassuk, Alexander G., Fritzsch, Bernd
Foilsithe / Cruthaithe 2013Téacs -
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Mechanisms of prickle1a function in zebrafish epilepsy and retinal neurogenesis de réir Mei, Xue, Wu, Shu, Bassuk, Alexander G., Slusarski, Diane C.
Foilsithe / Cruthaithe 2013Téacs -
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A Novel RPGR Mutation Masquerading as Stargardt Disease de réir Bassuk, Alexander G., Sujirakul, Tharikarn, Tsang, Stephen H., Mahajan, Vinit B.
Foilsithe / Cruthaithe 2014Téacs -
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Prickle1 regulates neurite outgrowth of apical spiral ganglion neurons but not hair cell polarity in the murine cochlea de réir Yang, Tian, Kersigo, Jennifer, Wu, Shu, Fritzsch, Bernd, Bassuk, Alexander G.
Foilsithe / Cruthaithe 2017Téacs -
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VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site de réir Tang, Peter H., Velez, Gabriel, Tsang, Stephen H., Bassuk, Alexander G., Mahajan, Vinit B.
Foilsithe / Cruthaithe 2019Téacs -
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Optical Coherence Tomography Angiography of RPGR-Associated Retinitis Pigmentosa Suggests Foveal Avascular Zone is a Biomarker for Vision Loss de réir Tang, Peter H., Jauregui, Ruben, Tsang, Stephen H., Bassuk, Alexander G., Mahajan, Vinit B.
Foilsithe / Cruthaithe 2019Téacs -
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Exome Sequencing Reveals RAG1 Mutations in a Child with Autoimmunity and Sterile Chronic Multifocal Osteomyelitis Evolving into Disseminated Granulomatous Disease de réir Reiff, Andreas, Bassuk, Alexander G., Church, Joseph A., Campbell, Elizabeth, Bing, Xinyu, Ferguson, Polly J.
Foilsithe / Cruthaithe 2013Téacs -
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BESTROPHIN1 mutations cause defective chloride conductance in patient stem cell-derived RPE de réir Moshfegh, Yasmin, Velez, Gabriel, Li, Yao, Bassuk, Alexander G., Mahajan, Vinit B., Tsang, Stephen H.
Foilsithe / Cruthaithe 2016Téacs