John Belmont
www.bcm.edu
0000-0001-7409-3578
Illumina Inc
183 papers found
Refreshing results…
DNA deletion confined to the iduronate-2-sulfatase promoter abolishes IDS gene expression
Comparative sequence analysis of a gene-rich cluster at human chromosome 12p13 and its syntenic region in mouse chromosome 6
Localization of BRRN1, the Human Homologue ofDrosophila barr,to 2q11.2
Protection of Primary Human T Cells from HIV Infection by Trev: A Transdominant Fusion Gene
Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains
Differential mRNA display using anchored oligo-dT and long sequence-specific primers as arbitrary primers
Genetic control of X inactivation and processes leading to X-inactivation skewing
A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome.
In Vivo Marking of Spontaneous or Vaccine-Induced Fibrosarcomas in the Domestic House Cat, Using an Adenoviral Vector Containing a Bifunctional Fusion Protein, GAL-TEK
Sixty-nine kilobases of contiguous human genomic sequence containing the ?-galactosidase A and Bruton's tyrosine kinase loci
Disruption of the adenosine deaminase gene causes hepatocellular impairment and perinatal lethality in mice.
Mild phenotypic effects of a de novo deletion Xpter→Xp22.3 and duplication 3pter→3p23
Insights into lymphocyte development from X-linked immune deficiencies
Inhibition of HIV-1 by a double transdominant fusion gene
Identification of soluble and membrane-bound isoforms of the murine flt3 ligand generated by alternative splicing of mRNAs
The receptor tyrosine kinase-related gene (ryk) demonstrates lineage and stage-specific expression in hematopoietic cells
Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12.
Delivery of a Secretable Adenosine Deaminase Through Microcapsules — A Novel Approach to Somatic Gene Therapy
Parental origin of the extra chromosomes in polysomy X
The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia
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