Associated Papers
Investigating the Structural and Functional Consequences of Pathogenic SNPs on Human VEGFA Dimer: Insights from Molecular Dynamics Study.
Islam R et al.
Acs Omega, 2025
41244458 (PubMed )
Supplement: ao5c07106_si_001.pdf
Common and rare variants in patients with early onset drusen maculopathy.
de Breuk A et al.
Clinical Genetics, 2022
36053979 (PubMed )
Supplement: CGE-102-414-s006.xlsx › Blad_1
A transcriptional network of cell cycle dysregulation in noninvasive papillary urothelial carcinoma.
Warrick JI et al.
Scientific Reports, 2022
36192513 (PubMed )
Supplement: 41598_2022_20927_MOESM14_ESM.xlsx › mutations
Case Report: A Novel Mutation Identified in CHST14 Gene in a Fetus With Structural Abnormalities.
Zhou YY et al.
Frontiers in Genetics, 2022
35464846 (PubMed )
Supplement: Table1.xlsx › DX1515_20D2319547R
Mutation analysis of the SDHD gene in four kindreds with familial paraganglioma: description of one novel germline mutation.
Velasco A et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B, 2005
p53 alterations and their relationship to SDHD mutations in parasympathetic paragangliomas.
van Nederveen FH et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc, 2003
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