about
If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism.Deletion of the basement membrane heparan sulfate proteoglycan type XVIII collagen causes hypertriglyceridemia in mice and humansNovel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome.Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations.Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells.Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders.Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello SyndromeWnt/β-catenin signaling and Msx1 promote outgrowth of the maxillary prominences.FGFR2 mutation confers a less drastic gain of function in mesenchymal stem cells than in fibroblasts.Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment.Effect of polymorphisms of the MTHFR and APOE genes on susceptibility to diabetes and severity of diabetic retinopathy in Brazilian patients.Functional Vascular Endothelial Growth Factor -634G>C SNP Is Associated With Proliferative Diabetic Retinopathy: A case-control study in a Brazilian population of European ancestry
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Erika Yeh
@ast
Erika Yeh
@en
Erika Yeh
@es
Erika Yeh
@nl
Erika Yeh
@sl
type
label
Erika Yeh
@ast
Erika Yeh
@en
Erika Yeh
@es
Erika Yeh
@nl
Erika Yeh
@sl
prefLabel
Erika Yeh
@ast
Erika Yeh
@en
Erika Yeh
@es
Erika Yeh
@nl
Erika Yeh
@sl
P106
P1153
15838348300
P21
P31
P496
0000-0002-2374-1528