J
John W. Belmont
Researcher at Baylor College of Medicine
Publications - 284
Citations - 42331
John W. Belmont is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Population & Gene. The author has an hindex of 76, co-authored 273 publications receiving 39393 citations. Previous affiliations of John W. Belmont include Boston Children's Hospital & University of Texas MD Anderson Cancer Center.
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Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects.
Jason R. Cowan,Jason R. Cowan,Muhammad Tariq,Muhammad Tariq,Chad A. Shaw,Mitchell Rao,John W. Belmont,Seema R. Lalani,Teresa A. Smolarek,Stephanie M. Ware +9 more
TL;DR: The results confirm a high CNV yield for array-based testing in patients with heterotaxy, and support use of CNV analysis for identification of novel biological processes relevant to human laterality.
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Protection of Primary Human T Cells from HIV Infection by Trev: A Transdominant Fusion Gene
TL;DR: This work showed that Trev was able to inhibit HIV replication in primary CD4+ T cells, and, therefore, the trev gene could be a candidate for gene therapy against HIV.
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Characterization of the interactions of human ZIC3 mutants with GLI3.
TL;DR: In vitro interactions of ZIC3 with GLI3 and the effect of Zic3 mutations identified in patients with either heterotaxy or isolated cardiovascular malformations are investigated.
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Basal ganglia calcifications in a case of biotinidase deficiency.
TL;DR: This report reports the first case of biotinidase deficiency with basal ganglia calcifications in patients with biotin-deficient state, with no symptoms referable to basalganglia dysfunction.
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Identification and cloning of differentially expressed genes by long-distance differential display.
TL;DR: Coupled with high-throughput cDNA sequencing and multiplex hybridization of cDNA microarrays for confirmation of differential expression, LDD-PCR could prove to be useful for simultaneous scanning of transcripts from multiple cDNA samples and faster selection of differentially expressed transcripts of interest.