Zobrazeno 1 - 6
of 6
pro vyhledávání: '"D. N. Stivers"'
Publikováno v:
Arthritis and rheumatism. 43(5)
Abnormalities of transforming growth factor beta (TGFbeta) and platelet-derived growth factor (PDGF) alpha and beta and/or their receptors have been demonstrated in systemic sclerosis (SSc). This study aimed to determine whether genetic polymorphisms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89c01c04b61b0d588724a2ca5506f56f
https://pubmed.ncbi.nlm.nih.gov/10817561
https://pubmed.ncbi.nlm.nih.gov/10817561
Publikováno v:
Tissue antigens. 53(1)
Choctaw Native Americans in southeastern Oklahoma have the highest prevalence of scleroderma or systemic sclerosis yet found (469/100,000). An Amerindian HLA DR2 haplotype (DRB1*1602) was significantly associated with scleroderma in this population i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2cbcdaaba1457e871ca7ffffae9d285
https://pubmed.ncbi.nlm.nih.gov/10082433
https://pubmed.ncbi.nlm.nih.gov/10082433
Publikováno v:
Arthritis and rheumatism. 41(10)
To localize disease genes for scleroderma, or systemic sclerosis (SSc), in a population of Choctaw Native Americans with a high prevalence of SSc, in which there is evidence of a possible founder effect.A candidate gene approach was used in which mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e4571a77f466665c60c3d3636246979
https://pubmed.ncbi.nlm.nih.gov/9778214
https://pubmed.ncbi.nlm.nih.gov/9778214
Publikováno v:
American journal of human genetics. 59(1)
Myotonic dystrophy (DM), an autosomal dominant neuromuscular disease, is caused by a CTG-repeat expansion, with affected individuals having > or = 50 repeats of this trinucleotide, at the DMPK locus of human chromosome 19q13.3. Severely affected indi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1298ca5fd1d76329603649ff8e789c07
https://pubmed.ncbi.nlm.nih.gov/8659513
https://pubmed.ncbi.nlm.nih.gov/8659513
Autor:
R, Chakraborty, D N, Stivers
Publikováno v:
Journal of forensic sciences. 41(4)
In parentage testing when one parent is excluded, the distribution of the number of loci showing exclusion due to mutations of the transmitting alleles is derived, and it is contrasted with the expected distribution when the exclusion is caused by no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a168de04a41f503a88607d78da4d5038
https://pubmed.ncbi.nlm.nih.gov/8754581
https://pubmed.ncbi.nlm.nih.gov/8754581
Autor:
Cristina Albarrán, Antonio Alonso, Ranjan Deka, D. N. Stivers, P. Martín, O. García, Ranajit Chakraborty, M. Sancho
Publikováno v:
16th Congress of the International Society for Forensic Haemogenetics (Internationale Gesellschaft für forensische Hämogenetik e.V.), Santiago de Compostela, 12–16 September 1995 ISBN: 9783540604921
Variable number of tandem repeats (VNTR) loci are highly informative markers for linkage analysis and identity testing. In addition to the variation in the number of repeats, some VNTR loci display variabilty of the repeat sequence so that an additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24453eb31427b03cd811d4c7cbad99c6
https://doi.org/10.1007/978-3-642-80029-0_39
https://doi.org/10.1007/978-3-642-80029-0_39
