Zobrazeno 1 - 10
of 235
pro vyhledávání: '"B. Carritt"'
Publikováno v:
Vox Sanguinis. 77:159-163
This study provides a unique method for identifying individuals carrying the Rh haplotype cDe, and supports a model for the evolution of Rh haplotypes in which cDe is the progenitor.DNA from 212 unrelated donors of known Rh serological phenotype was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39fdbc4fc84764e2d045609856787619
https://doi.org/10.1046/j.1423-0410.1999.7730159.x
https://doi.org/10.1046/j.1423-0410.1999.7730159.x
Autor:
Fiona K. Gould, B. Carritt, Lorie A. Stuart, Susan A. McDowell, Susan E. Waltz, Sandra J. Friezner Degen
Publikováno v:
DNA Sequence. 8:409-413
The human chromosome 3 locus coding for hepatocyte growth factor-like protein/macrophage stimulating protein (HGFL/MSP) is homologous to two sets of amplified loci on human chromosome 1 at lp36. One copy of one of the amplified loci (D1F15S1 A) has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46118ed6ac7f96edec56e7be25109e37
https://doi.org/10.3109/10425179809020903
https://doi.org/10.3109/10425179809020903
Evolution of the Human RH (Rhesus) Blood Group Genes: A 50 Year Old Prediction (Partially) Fulfilled
Publikováno v:
Human Molecular Genetics. 6:843-850
Almost exactly 50 years ago, R. A. Fisher and R. Race proposed a model for the evolution of the RH (rhesus) genes in which the less common haplotypes were derived from the commoner ones by recombination, and in which the gene order was D-C-E. No dire
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a22ffdddae56c9d35b84f6ed75fad4a
https://doi.org/10.1093/hmg/6.6.843
https://doi.org/10.1093/hmg/6.6.843
Publikováno v:
British Journal of Haematology. 94:417-421
Denaturing gradient gel electrophoresis (DGGE) was carried out on PCR products amplified from exons 2 and 5 of RHD and RHCE. Exon 2 of RHD and exon 2 of the C allele of RHCE have an identical sequence, which differs from that of the c allele of RHCE.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a33c7e568f4901f1fbb2e111f6a9d652
https://doi.org/10.1046/j.1365-2141.1996.d01-1808.x
https://doi.org/10.1046/j.1365-2141.1996.d01-1808.x
Publikováno v:
Immunohematology. 12:154-159
Initial Rh phenotyping of a man with hemolytic anemia, his wife, and son appeared to exclude paternity. No exclusion was found in other blood groups or in the human leukocyte antigen (HLA) system; excluding Rh, the paternity index was 98.58 percent.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82978c4661407fb77ccfedf5bb9939a4
https://doi.org/10.21307/immunohematology-2019-770
https://doi.org/10.21307/immunohematology-2019-770
Publikováno v:
Vox Sanguinis. 67:397-401
We have studied the RH genes in donors with the RhD-negative haplotype dCes. In contrast to the usual arrangement of genes in RhD-negative individuals, where the lack of antigen expression is due to deletion of the entire RHD gene, we find that the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2b143c1269943e042e5e59399b74b5d
https://doi.org/10.1111/j.1423-0410.1994.tb01280.x
https://doi.org/10.1111/j.1423-0410.1994.tb01280.x
Autor:
G. Gimelli, N.D. Avent, M. Pecorara, L. Ferrara, K. Inoue, R.L. Eddy, M. Acquila, D. Caprino, Y. Itoh, T. Hori, C. Panarello, B. Dutrillaux, C. MacGeoch, D. Patterson, P.J. Taylor, M.J.A. Tanner, T. Rangel-Figueiredo, M.J. Higgins, N.K. Spurr, M.A. Roberts, V. Natarajan, E. Takahashi, V. Hansson, P.G. Mori, S. Wood, E. Viegas-Péquignot, C.M. Baker, X. Zhu, J.M. Dunn, M. Salminen, L. Galleni, J.S. Simard, L. Iannuzzi, K. Hielscher, J.L. Longmire, D. Bérubé, T. Jahnsen, T. Abe, A. Shiels, C.S. Griffin, R. Stanyon, C.J. Mitchell, H. Adachi, N. Lemieux, D. Ayusawa, A. Becker, F.A. van der Hoeven, K. Ridgwell, G.P. Di Meo, L. Santini, S.K. Mahadevaiah, J.A. Meester, H. Nakazato, N.S-F. Ma, G. Giordano, K. Lundström, T.B. Shows, B.U. Zabel, H. Drabkin, K. Willan, R. Samjaa, K. Zernahle, B.L. Gallie, S. Misawa, P. de Boer, M. Hirsch-Kauffmann, H. Nakagawa, S.F. Lockwood, R. Winqvist, R. Gagné, K. Kashima, L.L. Deaven, R.A. Phillips, J.M.G.M. Schöller, S. Ørstavik, R. Schneider, S.K. Kaneda, M. Laatikainen, A. Tellini, I. Ulmanen, B. Carritt, D. Kieninger, A. Stubbe, T. Seno, E. Schneider-Scherzer, M. Schweiger, U. Mittwoch, G. Contrafatto, U. Walter, A.D. Goddard, J.A. Squire, J.N. Derr, M. Sandberg, J. Inazawa, M. Schertzer
Publikováno v:
Cytogenetic and Genome Research. 59:I-VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d054284e9d171d8caebeb68131715644
https://doi.org/10.1159/000133258
https://doi.org/10.1159/000133258
Autor:
J. Peters, A. Schinzel, Christopher J. Rawlings, J.L. Mandel, M. Tolley, S. Mercer, B. Byth, M.V. Bell, S. Povey, D. Goudie, N.C. Dracopoli, A. Geurts van Kessel, B.J.B. Keats, I.W. Craig, J. Schmidtke, T. Gedde-Dahl, P. Williamson, C. Junien, E. Solomon, C.J. Rawlings, F. Ricciuti, M. Farrall, S.T. Reeders, M.T Davisson, N.E. Simpson, S.L. Sherman, J. Weissenbach, S. Trumper, D.P. Doolittle, V. Reed, S. Malcolm, D.J. Cockburn, A. Hare, N.K. Spurr, Veronica van Heyningen, D.C. Wallace, R.H.Y. Lam, G.B. van Ommen, A.L. Hillyard, J. Ott, R.L. Nussbaum, J.M. Shoffner, H. Donis-Keller, C.E. Hildebrand, S. Malik, G. Gillett, R. Daniels, F. Mitelman, K.E. Davies, B. Maidak, A.M. Bowcock, J.A. Marshall Graves, P. Pearson, J. Walters, B. Carritt, B.S. Emanuel, T. Doyle, R.E. Lucier, S. Riley, R. Williamson, D. Lindenbaum, Y. Nakamura, J. Borrow, J.M. Trent, T.A. Donlon, C. Jones, A.G. Searle, G.R. Sutherland, L.-C. Tsui, L.C. Stranc, Steve Laval, R.T. Taggart, Sir Walter F. Bodmer, M.T Lott, P. Goodfellow, N. Shimizu, E. Keirnan, Baule, D.T. Bishop, S. Renfrey, M. Leppert, S. Ruddy, M. Barnett, P.J. McAlpine, J.C. Murray, K. Kidd, Y. Kaneko, H.F. Willard, A.P. Monaco, J. Hewitt, Y. Boyd, Z. Chen, H.H. Ropers, H. Cann, C. Boucheix, F. Lewitter, H.S. Chan, S. Ghosh, D.N. Cooper, S.L. Naylor, A. Torroni, C. Porter, G.M. Hampton, C. Westbrook, V. Buckle, M. Chipperfield, T. Morris, M.A. Pericak-Vance, K.H. Grzeschik, J. Frézal, L.L. Field, L. Sefton, W.O. McBride, P.A. Lalley, S.P. Craig, A. Bowcock, R.R. Ali, A. Ziegler, M. Quitt, S.J. O'Brien, D.W. Cox, K. Cooper, M.H. Skolnick, D.R. Cox, M M Le Beau, T.B. Shows, A. Walley, D.H. Ledbetter, K. Gulati, B.R. Seizinger, R. Track, T. Ward, G.A. Bruns, A.Y. Sakaguchi
Publikováno v:
Cytogenetic and Genome Research. 55:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61bbbb93956558230d04586577e5a4a0
https://doi.org/10.1159/000132996
https://doi.org/10.1159/000132996
Publikováno v:
American journal of human genetics. 59(5)
We have studied the arrangement of Rh (rhesus) genes in donors who are completely null for the products of one of them, RHCE. We show that five of six homozygous individuals with the so-called Rh D-- phenotype, who express no red-cell antigens of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9452067dd2126246cbbc0a9ec0770b48
https://pubmed.ncbi.nlm.nih.gov/8900235
https://pubmed.ncbi.nlm.nih.gov/8900235
Publikováno v:
Immunohematology. 12(4)
Initial Rh phenotyping of a man with hemolytic anemia, his wife, and son appeared to exclude paternity. No exclusion was found in other blood groups or in the human leukocyte antigen (HLA) system; excluding Rh, the paternity index was 98.58 percent.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9cb0cc5c6304b2c998c33adca092312
https://pubmed.ncbi.nlm.nih.gov/15387727
https://pubmed.ncbi.nlm.nih.gov/15387727