Zobrazeno 1 - 10
of 106
pro vyhledávání: '"I, Roisenberg"'
Polymorphisms in genes MTHFR, MTR and MTRR are not risk factors for cleft lip/palate in South Brazil
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 40, Iss 6, Pp 787-791 (2007)
Non-syndromic cleft lip and palate (CL/P) occurs due to interaction between genetic and environmental factors. Abnormalities in homocysteine metabolism may play a role in its etiology due to polymorphisms in genes involved in this pathway. Because of
Externí odkaz:
https://doaj.org/article/708930560ff247278747d3fa1a04b423
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 38, Iss 2, Pp 221-225 (2005)
Diabetic retinopathy (DR) is a sight-threatening chronic complication of diabetes mellitus and is the leading cause of acquired blindness in adults. In this cross-sectional study, we investigated the prevalence of and the factors associated with DR i
Externí odkaz:
https://doaj.org/article/3625d7eb0da34301b9dc1ac86db9d884
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 36, Iss 6, Pp 709-714 (2003)
High levels of von Willebrand factor (vWF) have been associated with cardiovascular disease. The A allele of the -1185A/G polymorphism in the 5'-regulatory region of the vWF gene was associated with the highest plasma vWF levels in a normal populatio
Externí odkaz:
https://doaj.org/article/b821c7dac0e440f1933b7632a5b1f737
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 34, Iss 9, Pp 1125-1129 (2001)
von Willebrand factor (vWF) is a protein that mediates platelet adherence to the subendothelium during primary hemostasis. High plasma vWF concentrations have been reported in patients with various types of cancer, such as head and neck, laryngeal an
Externí odkaz:
https://doaj.org/article/4096d97393af41c49847bd287cc1bb8d
Publikováno v:
Clinical endocrinology. 57(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9869d8da993b4bb64cc2b327f8e3fbd
https://pubmed.ncbi.nlm.nih.gov/12100083
https://pubmed.ncbi.nlm.nih.gov/12100083
Publikováno v:
Human biology. 72(6)
Von Willebrand factor gene polymorphisms were studied in three Brazilian ethnic groups: Euro-Brazilians, Afro-Brazilians, and Amerindians. Six polymorphic sites were analyzed: RsaI (exon 18), NlaIV (exon 20), HphI, KpnI, D1472H, and V1565L (all four
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5cbfcaae1491adfbe8fa18b3fb1ee827
https://pubmed.ncbi.nlm.nih.gov/11236861
https://pubmed.ncbi.nlm.nih.gov/11236861
Publikováno v:
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas. 29(12)
A simple method for the preparation of rabbit antiserum against human von Willebrand factor (vWF) from commercial lyophilized factor VIII concentrate is described. vWF antigen (vWFAg)-like protein was obtained by gel filtration of the concentrate on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::589c4cf89013d5f5bda81637457533bf
https://pubmed.ncbi.nlm.nih.gov/9222425
https://pubmed.ncbi.nlm.nih.gov/9222425
Publikováno v:
Annals of Human Genetics. :060721082338043
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79b0d71f3677d960a5e3df8805fcc9c0
https://doi.org/10.1111/j.1529-8817.2005.00249.x
https://doi.org/10.1111/j.1529-8817.2005.00249.x
Publikováno v:
The American Journal of Medicine. 40:628-633
A Brazilian family is described in which three members were found to have Rotor's syndrome, as indicated by history, laboratory studies and liver biopsy. The disease in this family, from which relevant information was obtained from seventy-two relati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::475c905963592601f1208fdb977844c8
https://doi.org/10.1016/0002-9343(66)90124-0
https://doi.org/10.1016/0002-9343(66)90124-0
Publikováno v:
Acta geneticae medicae et gemellologiae. 11:55-70
SUMMARYA description is made of a large Brazilian family of white ancestry in which some individuals presented polydactyly, other spherocytosis, and some both anomalies together. The information obtained involves five generations totaling 117 related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d509abe7e6ce1a80cce7dc16be355932
https://doi.org/10.1017/s112096230002045x
https://doi.org/10.1017/s112096230002045x