Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Payam Mahboubi"'
Restriction Enzyme–Mediated Enhanced Detection of Circulating Cell-Free Fetal DNA in Maternal Plasma
Publikováno v:
The Journal of Molecular Diagnostics. 13:382-389
A universal method confirming the presence of circulating cell-free fetal (ccff) DNA in maternal plasma is important in the field of noninvasive prenatal diagnostics. Restriction endonuclease digestion of one allele of a single-nucleotide polymorphis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38e79928e9ad3dbe5634cfa4ca0f18c3
https://doi.org/10.1016/j.jmoldx.2011.02.001
https://doi.org/10.1016/j.jmoldx.2011.02.001
Autor:
Daniel T. O'Connor, Geert W. Schmid-Schönbein, Sushil K. Mahata, Nicholas J. Schork, Ryan S. Friese, Nitish R. Mahapatra, Payam Mahboubi
Publikováno v:
American Journal of Hypertension. 18:633-652
Genetic studies of essential hypertension, a complex, polygenic, and age-dependent disorder, have not been able to completely elucidate the genes responsible for development of the trait. We used a novel strategy to compare gene expression in the adr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8aafcf6fae63e1d6d4f62a2871e3dc9
https://doi.org/10.1016/j.amjhyper.2004.11.037
https://doi.org/10.1016/j.amjhyper.2004.11.037
Autor:
Nicholas J. Schork, Sushil K. Mahata, Ryan S. Fries, Daniel T. O'Connor, Geert W. Schmid-Schoenbein, Nitish R. Mahapatra, Payam Mahboubi
Publikováno v:
Hypertension. 43:1301-1311
The genetic basis of hypertension in the genetically/hereditary hypertensive (BPH/2) mouse strain is incompletely understood, although a recent genome scan uncovered evidence for several susceptibility loci. To probe the neuroendocrine transcriptome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b90b28f518f585f4eae3b1faeb90c15c
https://doi.org/10.1161/01.hyp.0000127708.96195.e6
https://doi.org/10.1161/01.hyp.0000127708.96195.e6
Autor:
Bruce A. Hamilton, Manjula Mahata, Daniel T. O'Connor, Mats Stridsberg, Gen Wen, Fangwen Rao, Peter E. Cadman, Nicholas J. Schork, Nitish R. Mahapatra, Sajalendu Ghosh, Payam Mahboubi, Douglas W. Smith, Sushil K. Mahata
Publikováno v:
The American Journal of Human Genetics. 74(2):197-207
The chromogranin/secretogranin proteins are costored and coreleased with catecholamines from secretory vesicles in chromaffin cells and noradrenergic neurons. Chromogranin A (CHGA) regulates catecholamine storage and release through intracellular (ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d2d873565956d82101d324c5e15d8eb
Autor:
Daniel T. O'Connor, Payam Mahboubi, Sushil K. Mahata, Nitish R. Mahapatra, Clifford Wong, Manjula Mahata, Surin Chitbangonsyn
Publikováno v:
Physiological Genomics. 14:83-93
Hypertension is a complex trait with multiple genetic determinants. A previous genome-wide linkage study of systolic blood pressure in a mouse genetic backcross implicated a region of chromosome 13 (LOD = 3.3 at 16.0 cM) as a determinant of blood pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd898f00da0fbb2d242c62a4afc38bab
https://doi.org/10.1152/physiolgenomics.00162.2002
https://doi.org/10.1152/physiolgenomics.00162.2002
Autor:
David S. Timberlake, D Walker, S W Chitbangonsyn, Payam Mahboubi, K L Diggle, Robert J. Parmer, Brinda K. Rana, Daniel T. O'Connor
Publikováno v:
Journal of Human Hypertension. 17:319-324
Allelic variation at multiple genetic loci may contribute to hypertension. Since autonomic/sympathetic dysfunction may play an early, pathogenic, heritable role in hypertension, we evaluated candidate loci likely to contribute to such dysfunction, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2050319cae0bce0d4fc3c1ea6d4107
https://doi.org/10.1038/sj.jhh.1001550
https://doi.org/10.1038/sj.jhh.1001550
Publikováno v:
Genomics. 53(1)
We have developed a rapid screening method for cross-species amplification of homologous microsatellite loci and studied some of the characteristics of those loci in the species of origin (human) and the test species (baboon). We tested a matrix of 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e62c488d3a8fce589b9dd615f8e588ed
https://pubmed.ncbi.nlm.nih.gov/9787073
https://pubmed.ncbi.nlm.nih.gov/9787073