Publication Venue For
Genome-wide analysis of genetic alterations in testicular primary seminoma using high resolution single nucleotide polymorphism arrays.
Redefining regulation of DNA methylation by RNA interference.
Single nucleotide polymorphisms affect both cis- and trans-eQTLs.
Comparative genomic and phylogenetic analysis of short-chain dehydrogenases/reductases with dual retinol/sterol substrate specificity.
Genome-wide detection of LOH in prostate cancer using human SNP microarray technology.
Identification of FOXC1 as a TGF-β1 responsive gene and its involvement in negative regulation of cell growth.
Structural conservation of the genes encoding CaT1, CaT2, and related cation channels.
Mutations in Cdh23 Cause Nonsyndromic Hearing Loss in waltzer Mice.
Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES.
Isolation and preliminary characterization of the human and mouse homologues of the bacterial cell cycle gene Era.
Erratum: The uroguanylin gene (Guca1b) is linked to guanylin (Guca2) on mouse chromosome 4 (Genomics (1997) 45:2 (348-354)).
Closing in on the BPES gene on 3q23: Mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) Breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and β'-COP, distal to the breakpoint.
Assembly of a BAC contig of the complementation group B cell senescence gene candidate region at 4q33-q34.1 and identification of expressed sequences.
Genetic analysis of susceptibility to dextran sulfate sodium-induced colitis in mice.
Genomic cloning, molecular characterization, and functional analysis of human CLCA1, the first human member of the family of Ca2+-activated Cl- channel proteins.
Chromosome localization and genomic structure of the KiSS-1 metastasis suppressor gene (KISS1).
Genomic structure and chromosomal mapping of the nuclear orphan receptor RORγ (RORC) gene.
The human angiotensinase C gene (HUMPCP) maps to 11q14 within 700 kb of D11S901: A candidate gene for essential hypertension.
Identification and characterization of the human homologue of SH3BP2, an SH3 binding domain protein within a common region of deletion at 4p16.3 Involved in bladder cancer.
cDNA cloning, genomic structure, and chromosome mapping of the human epithelial membrane protein CL-20 gene (EMP1), a member of the PMP22 family.
The uroguanylin gene (Guca1b) is linked to guanylin (Guca2) on mouse chromosome 4.
Gene structure and chromosome localization to 7q21.3 of the human rod photoreceptor transducin γ-subunit gene (GNGT1).
The mouse BP-1 gene: Stucture, chromosomal localization, and regulation of expression by type I interferons and interleukin-7.
cDNA, gene structure, and chromosomal localization of human GAR1 (CNCG3L), a homolog of the third subunit of bovine photoreceptor cGMP-gated channel.
A novel creb family gene telomeric of HLA-DRA in the HLA complex.
Feature mapping of the HLA class I region: Localization of the POU5F1 and TCF19 genes.
Mapping of guanylin to murine chromosome 4 and human chromosome 1p34-p35.
Localization of the α2-Macroglobulin Receptor-Associated Protein 1 Gene (LRPAP1) and Other Gene Fragments to Human Chromosome 4p16.3 by Direct cDNA Selection.
A yac contig of approximately 3 mb from human chromosome 5q31 → q33.
Genomic sequence of the murine guanylin gene.
Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1.
Chromosomal Localization of Five Murine HSP70 Gene Family Members: Hsp70.1, Hsp70-2, Hsp70-3, Hsc70t, and Grp78.
Highly informative typing of the human TNF locus using six adjacent polymorphic markers.
Mapping of the glycoprotein 330 (gp330) gene to mouse chromosome 2.
Mitochondrial dna variants observed in alzheimer disease and parkinson disease patients.
Rapid identification of VNTR alleles of the human thyroid peroxidase gene by PCR: A study in a population sample from south Italy.
A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus.
Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase β-subunit gene in mouse and human: Tight linkage to the Huntington disease region (4p16.3).
Exclusion of linkage between hypokalemic periodic paralysis (HOKPP) and three candidate loci.
Mapping of the mouse Rxr loci encoding nuclear retinoid X receptors RXRα, RXRβ, and RXRγ.
Syntenic assignments of visual transduction genes in cattle.
A map of the distal region of the long arm of human chromosome 21 constructed by radiation hybrid mapping and pulsed-field gel electrophoresis.
Characterization of the 3′ half of the human type IV collagen α5 gene that is affected in the Alport syndrome.
Localization of the expressed human p58 protein kinase chromosomal gene to chromosome 1p36 and a highly related sequence to chromosome 15.
Molecular linkage of the HLA-DR, HLA-DQ, and HLA-DO genes in yeast artificial chromosomes.
Physical mapping of yeast artificial chromosomes containing sequences from the human β-globin gene region.
Genetic linkage of the human apolipoprotein AI-CIII-AIV gene cluster and the neural cell adhesion molecule (NCAM) gene.
Molecular characterization of human and bovine rod photoreceptor cGMP phosphodiesterase α-subunit and chromosomal localization of the human gene.
Molecular cloning of the t complex responder genetic locus.
Huntington disease: No evidence for locus heterogeneity.
Isolation and field-inversion gel electrophoresis analysis of DNA markers located close to the Huntington disease gene.
Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid.
Nucleotide sequence and expression of the human skeletal α-actin gene: Evolution of functional regulatory domains.
Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17.