Search Results - "MCALPINE, P. J"

Guidelines for human gene nomenclature (1997) by WHITE, J. A, MCALPINE, P. J, PETERS, J, SCOTT, A, SCOTT, H, SPURR, N, TALBOT, C. JR, POVEY, S, ANTONARAKIS, S, CANN, H, EPPIG, J. T, FRAZER, K, FREZAL, J, LANCET, D, NAHMIAS, J, PEARSON, P

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The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26 by Allderdice, P W, Gardner, H A, Galutira, D, Lockridge, O, LaDu, B N, McAlpine, P J

“…Human tissues have two distinct cholinesterase activities: acetylcholinesterase and butyrylcholinesterase. Acetylcholinesterase functions in the transmission…”
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Genetic diversity among Canadienne, Brown Swiss, Holstein, and Jersey cattle of Canada based on 15 bovine microsatellite markers by Hansen, C, Shrestha, J N B, Parker, R J, Crow, G H, McAlpine, P J, Derr, J N

“…The genetic diversity among Canadienne, Brown Swiss, Holstein, and Jersey cattle was estimated from relationships determined by genotyping 20 distantly related…”
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Identification of an E689K substitution as the molecular basis of the human acid alpha-glucosidase type 4 allozyme (GAA4) by Huie, M L, Menaker, M, McAlpine, P J, Hirschhorn, R

“…We have identified the molecular basis of the GAA*4 allozyme as a G to A transition at nt2065 which predicts the substitution of glutamic acid by lysine at…”
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Assignment of the gene(s) governing Froese and Swann blood group polymorphism to chromosome 17q by Zelinski, T, McKeown, I, McAlpine, P J, Philipps, S, Coghlan, G

“…The red cell antigens Fra and Swa were first described in 1978 and 1959, respectively. Despite the fact that these antigens are well defined serologically,…”
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Polymorphism detected by multiple RENS in the human coagulation factor II (F2) gene by MCALPINE, P. J, DICKSON, M, GUY, C, WIENS, A, IRWIN, D. M, MACGILLIVRAY, R. T. A

“…Clone pIIH13 has a 2.0 kb insert of F2 cDNA. PstI identifies alleles of 8.3 kb (A1) and 9.1 kb (A2) with constant bands of 1.8, 1.4 and 1.2 kb. The RFLP…”
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Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9 by ALLDERDICE, P. W, KAITA, H, LEWIS, M, MCALPINE, P. J, WONG, P, ANDERSON, J, GIBLETT, E. R

“…Cytogenetic, enzyme dosage, serological, and electrophoretic analyses of blood samples from members of three Newfoundland kindreds in which one specific…”
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The low-incidence red cell antigen Wra: genetic studies by Lewis, M, Kaita, H, Philipps, S, McAlpine, P J

“…Studies of 91 individuals in three families allowed a genetic-linkage analysis of the gene governing the production of the low-incidence red cell antigen Wra…”
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Evidence that SE is distal to LU on chromosome 19q by Zelinski, T, Coghlan, G, Greenberg, C R, McAlpine, P J, Lewis, M

“…Analysis of a family informative for chromosome 19 loci establishes that the Lutheran blood group locus (LU) lies between the third component of human…”
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The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPs by MCALPINE, P. J, DIXON, M, ALLDERDICE, P. W, LOCKRIDGE, O, LA DU, B. N

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The Colton blood group locus. A linkage analysis by Zelinski, T, Kaita, H, Lewis, M, Coghlan, G, Philipps, S, Belcher, E, McAlpine, P J, Coopland, G, Wong, P

“…Accumulated family information was compiled in an attempt to verify the chromosomal location of the Colton blood group locus (CO). Two-point linkage analysis…”
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An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosa by Hughes, H E, McAlpine, P J, Cox, D W, Philipps, S

“…A previously undescribed autosomal dominant syndrome has been observed in a large kindred with affected relatives spanning at least five generations. The…”
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Exclusion of unassigned blood group system loci from the regulator of complement activation gene cluster on chromosome 1q32 by Lewis, M, Kaita, H, Philipps, S, McAlpine, P J, Wong, P

“…Genetic linkage analyses of the blood group system loci CO, DI, DO, KEL and YT in relation to F13B indicate that these loci are not members of the RCA gene…”
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The 1990 catalog of mapped genes and report of the nomenclature committee by McAlpine, P J, Stranc, L C, Boucheix, C, Shows, T B

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Identification of an uncommon haptoglobin type using DNA and protein analysis by MARLES, S. L, MCALPINE, P. J, ZELINSKI, T, PHILLIPS, S, MAEDA, N, GREENBERG, C. R

“…The inherited variations in haptoglobin phenotypes are attributed to the homozygous and heterozygous combinations of three common autosomal alleles: HP*1F,…”
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The chromosome 19 linkage group LDLR, C3, LW, APOC2, LU, SE in man by Lewis, M, Kaita, H, Coghlan, G, Philipps, S, Belcher, E, McAlpine, P J, Coopland, G R, Woods, R A

“…The data establish linkage in both sexes for LDLR:LW (zeta = 8.43 at theta = 0.00) and in the male for LDLR:LU (zeta = 3.31 at theta = 0.00) and for LW:APOC2…”
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A New low incidence red cell antigen, NFLD by LEWIS, M, KAITA, H, ALLDERDICE, P. W, BERGREN, M, MCALPINE, P. J

“…A "new" low incidence red cell antigen, NFLD, is described. It was found in a Caucasian family and is inherited as an autosomal dominant. The antigen is not…”
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Coagulation factor XIII B subunit is encoded by a gene linked to the regulator of complement activation (RCA) gene cluster in man by RODRIGUEZ DE CORDOBA, S, REY-CAMPOS, J, DYKES, D. D, MCALPINE, P. J, WONG, P, RUBINSTEIN, P

“…The authors have performed linkage analysis to determine the genetic relationship between the loci coding for coagulation factor XIII B (F13B ) and the…”
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The 1985 Catalog of Mapped Genes and report of the Nomenclature Committee by McAlpine, P J, Shows, T B, Miller, R L, Pakstis, A J

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Cystic fibrosis: analysis of linkage of the disease locus to red cell and plasma protein markers by Tsui, L C, Cox, D W, McAlpine, P J, Buchwald, M

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