Zobrazeno 1 - 10 of 49 pro vyhledávání: '"Lowell R. Weitkamp"'
1
Equine marker genes: Polymorphism for plasminogen
Autor: S. A. Guttormsen, P. Costello‐Leary, Lowell R. Weitkamp
Publikováno v: Animal Blood Groups and Biochemical Genetics. 14:219-223
Polymorphism for two autosomal alleles of equine plasminogen, PLG1 and PLG2, was demonstrated in plasma by isoelectric focusing and immunofixation, with a goat anti-human plasminogen antibody. The frequency of PLG2 was 0.16 in 150 Standardbreds, 0.20
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45b15488ba25e3115c5f8b24c5143012
https://doi.org/10.1111/j.1365-2052.1983.tb01075.x
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2
Equine markers genes. Polymorphism for group-specific component (Gc)
Autor: Lowell R. Weitkamp
Publikováno v: Animal Blood Groups and Biochemical Genetics. 9:123-126
Polymorphism of equine Gc protein was demonstrated by immunofixation electrophoresis with a goat anti-human Gc antibody. Three different phenotypes, F, FS and S, were found. Family data supported the genetic theory of two autosomal codominant alleles
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a88e27f080857c3c581d10255df966f
https://doi.org/10.1111/j.1365-2052.1978.tb01422.x
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4
Discovery of allelic variants ofHOXA1 andHOXB1: Genetic susceptibility to autism spectrum disorders
Autor: Christopher J. Stodgell, Lowell R. Weitkamp, Jennifer L. Ingram, Susan L. Hyman, Patricia M. Rodier, Denise A. Figlewicz
Publikováno v: Teratology. 62:393-405
Background Family studies have demonstrated that the autism spectrum disorders (ASDs) have a major genetic etiologic component, but expression and penetrance of the phenotype are variable. Mice with null mutations of Hoxa1 or Hoxb1, two genes critica
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b604ae63c0a77c5f2084ba8b93e4c9a5
https://doi.org/10.1002/1096-9926(200012)62:6<393::aid-tera6>3.0.co
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6
Lean body mass in twins
Autor: Gilbert B. Forbes, Lowell R. Weitkamp, Eva Prochaska Sauer
Publikováno v: Metabolism. 44:1442-1446
A study of 49 pairs of monozygous (MZ) twins and 38 pairs of same-sexed dizygous (DZ) twins showed that lean body mass (LBM), as determined by potassium 40 counting, is under genetic influence. Intrapair variances for LBM are much smaller than those
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2981f46fc2832fbe6a0a43b45f727df5
https://doi.org/10.1016/0026-0495(95)90144-2
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7
A robust test for assortative mating
Autor: Lowell R. Weitkamp, Glenys Thomson, Carole Ober, Emmanuelle Génin
Publikováno v: European journal of human genetics : EJHG. 8(2)
Testing for random mating in human populations is difficult due to confounding factors such as ethnic preference and population stratification. With HLA, the high level of polymorphism is an additional problem since it is rare for couples to share th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36cd6ab7ebc7b07a111e848a9cbf0714
https://pubmed.ncbi.nlm.nih.gov/10757643
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9
Ancestral and recombinant 16-locus HLA haplotypes in the Hutterites
Autor: Lowell R. Weitkamp, Carole Ober
Publikováno v: Immunogenetics. 49(6)
Prior studies in the Schmiedeleut Hutterites of South Dakota have demonstrated associations between human leukocyte antigen (HLA) haplotype matching and fetal loss (Ober et al. 1992) and mate preferences (Ober et al. 1997), as well as deficiencies of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63eb98474bfc8afbf5d14ddec6cab3d3
https://pubmed.ncbi.nlm.nih.gov/10380692
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