Search Results - "Carritt, B."

Evolution of the Human RH (Rhesus) Blood Group Genes: A 50 Year Old Prediction (Partially) Fulfilled by Carritt, B., Kemp, T. J., Poulter, M.

“…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…”
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A recombination hot spot in the Rh genes revealed by analysis of unrelated donors with the rare D- phenotype by KEMP, T. J, POULTER, M, CARRITT, B

“…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…”
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Prenatal detection of fetal RhD DNA sequences in transcervical samples by Adinolfi, M, Sherlock, J, Kemp, T, Carritt, B, Soothill, P, Kingdom, J, Rodeck, C

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A Gene in the Chromosomal Region 3p21 with Greatly Reduced Expression in Lung Cancer is Similar to the Gene for Ubiquitin-Activating Enzyme by Kok, Klaas, Hofstra, Robert, Pilz, Alison, van den Berg, Anke, Terpstra, Peter, Charles H. C. M. Buys, Carritt, Ben

“…The chromosomal region 3p21 is thought to be the site of a lung tumor suppressor gene. We recently cloned a gene from this region that has greatly reduced…”
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Prenatal determination of fetal RhD type by Carritt, B, Steers, F J, Avent, N D

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Restriction fragment length polymorphisms in the D7S1 region of human chromosome 7 by CARRITT, B

“…A restriction fragment length polymorphism in the D7S1 region of chromosome 7 is detected by hybridizing the recombinant plasmid pA2H3 to HindIII- or…”
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Lack of RH C/E expression in the Rhesus D--phenotype is the result of a gene deletion by Blunt, T, Steers, F, Daniels, G, Carritt, B

“…We have investigated the arrangement of genes in the rare Rh (Rhesus) partial null condition D--. Southern blot and PCR studies under conditions which…”
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Chromosomal localization of human cellular homologues of two viral oncogenes by Heisterkamp, Nora, Groffen, John, Stephenson, John R, Spurr, N. K, Goodfellow, P. N, Solomon, E, Carritt, B, Bodmer, W. F

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Report of the committee on the genetic constitution of chromosomes 20 and 21 by Carritt, B, Litt, M

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Report of the sixth international workshop on human chromosome 3 mapping 1995 by Naylor, S L, Carritt, B, Boileau, C, Beroud, C, Alexander, C, Allderdice, P, Alimov, A, Ashworth, T, Bonifas, J, Bugert, P, Buys, C H, Chipperfield, M A, Deng, G, Drabkin, H, Gemmill, R M, Grompe, M, Joensuu, T, Jonasdottir, A, Gizatullin, R, Krols, L, Leach, R J, Lott, S T, Killary, A, Martinsson, T, Messiaen, L

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Sequences homologous to the human D1S1 locus present on human chromosome 3 by CARRITT, B, WELCH, H. M, PARRY-JONES, N. J

“…We have investigated the segregation, in somatic cell hybrids, of the human D1S1 locus, previously assigned to 1p36 by in situ hybridization. We have shown…”
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Somatic cell genetic evidence for the presence of a gene for citrullinemia on human chromosome 9 by Carritt, B

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A PCR-aided transcript titration assay revealing very low expression of a gene at band 3p21 in 33 cells lines derived from all types of lung cancer by Kok, K, van den Berg, A, Buchhagen, D L, Carritt, B, Buys, C H

“…We have developed a general PCR-based method to quantify the amount of a specific mRNA present in a given cell line or tissue. We applied this quantitative PCR…”
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An unusually proximal deletion on the short arm of chromosome 3 in a patient with small cell lung cancer by Daly, M C, Douglas, J B, Bleehen, N M, Hastleton, P, Twentyman, P R, Sundaresan, V, Carritt, B, Bergh, J, Rabbitts, P H

“…The tumors of patients with small cell lung carcinoma (SCLC) frequently exhibit the loss of alleles at polymorphic loci on the short arm of chromosome 3. We…”
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Report of the committee on the genetic constitution of chromosomes 20 and 21 by Carritt, B, Litt, M

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The SON gene encodes a conserved DNA binding protein mapping to human chromosome 21 by Khan, I M, Fisher, R A, Johnson, K J, Bailey, M E, Siciliano, M J, Kessling, A M, Farrer, M, Carritt, B, Kamalati, T, Buluwela, L

“…We report the identification and characterization of a clone for the DNA binding protein SON, which we have isolated from a human keratinocyte cDNA library…”
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The EUROGEM map of human chromosome 1 by Kumar-Singh, R, Wang, H, Carritt, B, Kruse, T A, McCarthy, T V, Vergnaud, G, Humphries, P

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Diverse Origins of Multiple Ovarian Teratomas in a Single Individual by Carritt, B., Parrington, J. M., Welch, H. M., Povey, S.

“…Centromere heteromorphisms and enzyme markers were examined in cells cultured from seven benign ovarian teratomas arising in a single patient. Three of the…”
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An α-fucosidase pseudogene on human chromosome 2 by CARRITT, B, WELCH, H. M

“…In Chinese hamster-human hybrids with overlapping translocations, the major site of hybridization of a cDNA clone for the liver form of human…”
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Report of the committee on the genetic constitution of chromosomes 20, 21, and 22 by Kaplan, J C, Carritt, B

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