Sheng-Jia Lin
Oklahoma Medical Research Foundation
22 papers found
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A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
UploadFront Cover, Volume 43, Issue 10
UploadWARS1 and SARS1 : Two tRNA synthetases implicated in autosomal recessive microcephaly
UploadRGS2 Suppresses Melanoma GrowthviaInhibiting MAPK and AKT Signaling Pathways
Download from doi.orgCnr2 Is Important for Ribbon Synapse Maturation and Function in Hair Cells and Photoreceptors
Download from doi.orgA biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
UploadBiallelic mutation of CLRN2 causes non-syndromic hearing loss in humans
UploadEpigenetic regulation of NOTCH1 and NOTCH3 by KMT2A inhibits glioma proliferation
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