Search Results - "Rao, P.Nagesh"

Localization of the Ileal Sodium-Bile Acid Cotransporter Gene (SLC10A2) to Human Chromosome 13q33 by Wong, Melissa H., Rao, P.Nagesh, Pettenati, Mark J., Dawson, Paul A.

“…Bile acids are synthesized from cholesterol in the liver and secreted into the small intestine, where they facilitate absorption of fat-soluble vitamins and…”
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Polymorphism and Chromosomal Localization of the GI-Form of Human Glutathione Peroxidase (GPX2) on 14q24.1 byin SituHybridization by Chu, Fong-Fong, Rohan de Silva, H.A., Esworthy, R.Steven, Boteva, Kalina K., Walters, Claire E., Roses, Allen, Rao, P.Nagesh, Pettenati, Mark J.

“…We have isolated a 3.3-kb DNA containing the two exons and a 2.6-kb intron of the humanGPX2gene. This gene encodes the intestinal isoenzyme of glutathione…”
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The human NACP/α-synuclein gene: chromosome assignment to 4q21.3–q22 and TaqI RFLP analysis by Chen, Xiaohua, de Silva, H.A.Rohan, Pettenati, Mark J., Rao, P.Nagesh, George-Hyslop, Peter St, Roses, Allen D., Xia, Yu, Horsburgh, Karen, Uéda, Kenji, Saitoh, Tsunao

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Characterization of Human and Mouse Rod cGMP Phosphodiesterase δ Subunit (PDE6D) and Chromosomal Localization of the Human Gene by Li, Ning, Florio, Stephanie K., Pettenati, Mark J., Rao, P.Nagesh, Beavo, Joseph A., Baehr, Wolfgang

“…The mammalian multisubunit photoreceptor cGMP phosphodiesterase PDEαβγ2(PDE6 family) is a peripherally membrane-associated enzyme. A novel subunit, termed PDEδ…”
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The Human PECAM1 Gene Maps to 17q23 by Gumina, Richard J., Kirschbaum, Nancy E., Rao, P.Nagesh, vanTuinen, Peter, Newman, Peter J.

“…We have determined the chromosomal and regional location of the gene encoding PECAM-1 (termed PECAM1 by GBD nomenclature) using a polymerase chain reaction…”
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cDNA sequence and gene locus of the human retinal phosphoinositide-specific phospholipase-Cβ4 (PLCB4) by ALVAREZ, R. A, GHALAYINI, A. J, PING XU, HARDCASTLE, A, SHOMI BHATTACHARYA, NAGESH RAO, P, PETTENATI, M. J, ANDERSON, R. E, BAEHR, W

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Molecular cytogenetic analysis of a duplication Xp in a male : further delineation of a possible sex influencing region on the X chromosome by RAO, P. N, KLINEPETER, K, STEWART, W, HAYWORTH, R, GRUBS, R, PETTENATI, M. J

“…We describe a male infant with severe mental retardation and autism with a duplication of the short arm of the X chromosome. Chromosome painting confirmed the…”
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Localization and Physical Mapping of Genes Encoding the A+U-Rich Element RNA-Binding Protein AUF1 to Human Chromosomes 4 and X by Wagner, Belinda J., Long, Laura, Rao, P.Nagesh, Pettenati, Mark J., Brewer, Gary

“…Messenger RNAs encoding many oncoproteins and cytokines are relatively unstable. Their instability, which ensures appropriate levels and timing of expression,…”
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Study of clonality in myelodysplastic syndromes: Detection of trisomy 8 in bone marrow cell smears by fluorescence in situ hybridization by Abruzzese, Elisabetta, Buss, David, Rainer, Robert, Rao, P.Nagesh, Pettenati, Mark J.

“…The lineage involvement in myelodysplastic syndromes (MDS) is still unclear. To determine the clonality and the evolution of the disorder, a retrospective…”
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Usefulness and limitations of serum and urine lysozyme levels in the classification of acute myeloid leukemia: An analysis of 208 cases by Sexton, Carol, Buss, David, Powell, Bayard, O'Connor, Michael, Rainer, Robert, Woodruff, Ralph, Cruz, Julia, Pettenati, Mark, Rao, P.Nagesh, Case, L.Douglas

“…The revised French-American-British (FAB) classification system for acute myeloid leukemia (AML) recommends the determination of serum lysozyme (SL) or urine…”
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Human endopeptidase (THOP1) is localized on chromosome 19 within the linkage region for the late-onset Alzheimer disease AD2 locus by MECKELEIN, B, ROHAN DE SILVA, H. A, ROSES, A. D, RAO, P. N, PETTENATI, M. J, PU-TING XU, HODGE, R, GLUCKSMAN, M. J, ABRAHAM, C. R

“…A cDNA encoding the rat endopeptidase 24.15 was used to determine the chromosomal localization of the respective human gene. Hybridization to DNA from…”
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Fructose-1,6-Bisphosphatase: Genetic and Physical Mapping to Human Chromosome 9q22.3 and Evaluation in Non-Insulin-Dependent Diabetes Mellitus by Rothschild, Cynthia B., Freedman, Barry I., Hodge, Rosa, Rao, P.Nagesh, Pettenati, Mark J., Anderson, Richard A., Akots, Gita, Qadri, Asif, Roh, Bong, Fajans, S.S., Reis, Andre, Morris, Deborah J., Usala, Anton, Hayward, Caroline, Brock, David, Colle, Eleanor, Spray, Beverly J., Rich, Stephen S., Bowden, Donald W.

“…PCR primers specific to the human liver fructose-1,6-bisphosphatase (FBP) gene were designed and used to isolate a cosmid clone. Physical mapping of the FBP…”
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Expression of fragile sites in childhood acute lymphoblastic leukemia patients and normal controls by NAGESH RAO, P, HEEREMA, N. A, PALMER, C. G

“…A high concordance has been reported between fragile sites and breakpoints involved in chromosomal rearrangements in cancer. A prospective study on the role of…”
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Identification of BCR-ABL Fusion on Chromosome 9 by Fluorescence In Situ Hybridization in Two Chronic Myeloid Leukemia Cases by Abruzzese, Elizabetta, Pettenati, Mark J., Cox, Kelly, Jackle, Bethy, Watts, Robert G., Carroll, Andrew J., Steuterman, Mary C., Rao, P.Nagesh

“…We present two cases with hidden Philadelphia translocations that resulted from an insertion and a complex translocation. These cases were unusual in having…”
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Monosomy X as a recurring sole cytogenetic abnormality associated with myelodysplastic diseases by Abruzzese, Elisabetta, Rao, P.Nagesh, Slatkoff, Mark, Cruz, Julia, Powell, Bayard L., Jackle, Bethy, Pettenati, Mark J.

“…Solitary loss of the X chromosome is associated with Turner syndrome and not hematological disorders. We describe five patients with non-constitutional loss of…”
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