Zobrazeno 1 - 10
of 19
pro vyhledávání: '"K W Klinger"'
Autor:
K W Klinger, Gregory M. Landes, Timothy D. Connors, Timothy C. Burn, William R. Dackowski, T J Van Raay, J. M. Millholland
Publikováno v:
Genome Research. 6:525-537
A 700-kb region of DNA in human chromosome 16p13.3 has been shown to contain the polycystic kidney disease 1 (PKD1) and the tuberous sclerosis type 2 (TSC2) disease genes. An estimated 20 genes are present in this region of chromosome 16. We have ini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36cbb2f7257ab65125da375aca71f67b
https://doi.org/10.1101/gr.6.6.525
https://doi.org/10.1101/gr.6.6.525
Autor:
Linda R. Petry, G.G. Germino, T J Van Raay, Timothy D. Connors, K W Klinger, Timothy C. Burn, Gregory M. Landes
Publikováno v:
Genome Science and Technology. 1:317-327
A pyrimidine-rich element (PyRE), present in the 21st intron of the PKD1 gene, posed a significant obstacle in determining the primary structure of the gene. Only cycle sequencing of nested, single-stranded phage templates of the CT-rich strand enabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4933bd30cb697faf03cf23b4881dd54f
https://doi.org/10.1089/mcg.1996.1.317
https://doi.org/10.1089/mcg.1996.1.317
Autor:
J. D. Valentich, M. J. Welsh, M. C. Iannuzzi, Shelley A. Grubman, Douglas M. Jefferson, K. W. Klinger, Ming Li, F. C. Marini, Henry L. Dorkin
Publikováno v:
American Journal of Physiology-Lung Cellular and Molecular Physiology. 259:L496-L505
Continuous epithelial cell lines from individuals with cystic fibrosis (CF) and normal controls are required to understand the genetic and cellular defects in CF. We used retroviruses to transduce SV40 large T antigen into nasal epithelial cells. Tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8416c10df854fa5ef6f14336ec46305d
https://doi.org/10.1152/ajplung.1990.259.6.l496
https://doi.org/10.1152/ajplung.1990.259.6.l496
Autor:
D W, Bianchi, J L, Simpson, L G, Jackson, S, Elias, W, Holzgreve, M I, Evans, K A, Dukes, L M, Sullivan, K W, Klinger, F Z, Bischoff, S, Hahn, K L, Johnson, D, Lewis, R J, Wapner, F, de la Cruz
Publikováno v:
Prenatal diagnosis. 22(7)
The National Institute of Child Health and Human Development Fetal Cell Isolation Study (NIFTY) is a prospective, multicenter clinical project to develop non-invasive methods of prenatal diagnosis. The initial objective was to assess the utility of f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f661683f84253cc72c95a5d29013bbc3
https://pubmed.ncbi.nlm.nih.gov/12124698
https://pubmed.ncbi.nlm.nih.gov/12124698
Autor:
Greg Landes, Tom I. Bonner, Heather W. Pinkett, Christiane M. Robbins, K W Klinger, Tim D. Connors, Andreas D. Baxevanis, Mezbah U. Faruque, Dietrich A. Stephan, John D. Carpten, Raman Sood, Jeffrey M. Trent, Izabela Makalowska, Christopher L. Graham, Kui Su, Sharon D. Morgenbesser
The aim of this study was to develop a saturated transcript map of the region encompassing the HPC1 locus to identify the susceptibility genes involved in hereditary prostate cancer (OMIM 176807) and hyperparathyroidism-jaw tumor syndrome (OMIM 14500
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a910bf402cca2fe6a6f6a5e4c9c655c4
https://zenodo.org/record/1229806
https://zenodo.org/record/1229806
Evaluation of DNA sequencing ambiguities using tetramethylammonium chloride hybridization conditions
Autor:
Timothy D. Connors, G.G. Germino, T. J. VanRaay, Timothy C. Burn, Gregory M. Landes, K W Klinger
Publikováno v:
BioTechniques. 22(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::457cbb7f4f8ed007d66b8c419168cbd7
https://pubmed.ncbi.nlm.nih.gov/9187758
https://pubmed.ncbi.nlm.nih.gov/9187758
Two isoforms of the human growth hormone receptor (hGHR), which differ in the presence (hGHRwt) or absence (hGHRd3) of exon 3, are expressed in the placenta. Specifically, three expression patterns are observed: only hGHRwt, only hGHRd3, or an approx
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3dee7328f9bfbee254e2097f890cdd2
https://europepmc.org/articles/PMC38002/
https://europepmc.org/articles/PMC38002/
Autor:
T, Bryndorf, B, Christensen, M, Vad, J, Parner, M P, Carelli, B E, Ward, K W, Klinger, J, Bang, J, Philip
Publikováno v:
American journal of human genetics. 59(4)
We developed a 1-d FISH assay for detection of numerical chromosome abnormalities in uncultured chorionic villus samples (CVS). Probes specific for chromosomes 13, 18, 21, X, and Y were used to determine ploidy by analysis of signal number in hybridi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec7cb4235098506662f8deab4deca5a2
https://pubmed.ncbi.nlm.nih.gov/8808609
https://pubmed.ncbi.nlm.nih.gov/8808609
Autor:
D W, Bianchi, K W, Klinger, T J, Vadnais, M A, Demaria, A P, Shuber, J, Skoletsky, P, Midura, M, Diriso, C, Pelletier, M, Genova, M S, Erikson, J M, Williams
Publikováno v:
Prenatal diagnosis. 16(4)
Three major methods have been described for the isolation of fetal cells from maternal blood: fluorescence-activated cell sorting (FACS), immunomagnetic beads, and magnetic-activated cell sorting (MACS). To date, no study has directly compared fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6484d9bddfdcb73bae05be902239f249
https://pubmed.ncbi.nlm.nih.gov/8734801
https://pubmed.ncbi.nlm.nih.gov/8734801