Cloning and functional expression of human retinal kir2.4, a pH-sensitive inwardly rectifying K(+) channel.

Genomic structure, expression, and chromosomal localization of the human glycine N-methyltransferase gene.

Structure, function, and genomic organization of human Na(+)-dependent high-affinity dicarboxylate transporter.

Expression profile and chromosomal location of cDNA clones, identified from an enriched adult retina library.

Human placental Na+-dependent multivitamin transporter. Cloning, functional expression, gene structure, and chromosomal localization.

Exon-intron structure, analysis of promoter region, and chromosomal localization of the human type 1 sigma receptor gene.

Familial dup(5)(q15q21) associated with normal and abnormal phenotypes.

Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YY.

A thyroid hormone receptor coactivator negatively regulated by the retinoblastoma protein.

Cytogenetic and molecular studies of a familial paracentric inversion of Y chromosome present in a patient with ambiguous genitalia.

A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization.

Characterization of the human type 2 neuropeptide Y receptor gene (NPY2R) and localization to the chromosome 4q region containing the type 1 neuropeptide Y receptor gene.

Cloning of the sodium-dependent, broad-scope, neutral amino acid transporter Bo from a human placental choriocarcinoma cell line.

Prenatal detection of two different monosomic cell lines by chorionic villus sampling.

Frequent spontaneous deletions at a shuttle vector locus in transgenic mice.

Genetic analysis of benign, low-grade, and high-grade ovarian tumors.

A polymorphic trinucleotide repeat at DXS8170 in the critical region of X-linked retinitis pigmentosa locus RP3 at Xp21.1.

Allelic deletion mapping of putative tumor suppressor genes on 17q in sporadic ovarian cancer.

Proton/peptide cotransporter (PEPT 2) from human kidney: functional characterization and chromosomal localization.

A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.