Zobrazeno 1 - 8
of 8
pro vyhledávání: '"I B, Larripa"'
Autor:
I. Szurkalo, L. C. Rossetti, Miguel Martin Abelleyro, Raúl Pérez Bianco, L. Primiani, C. P. Radic, M. de Tezanos Pinto, D. Neme, M. Candela, I. B. Larripa, C. D. De Brasi
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 19(4)
Inhibitor development against exogenous factor VIII is a severe impairment of replacement therapy affecting 18% of Argentine patients with severe haemophilia A (HA). To study the molecular predisposition for inhibitor development, we genotyped 260 HA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c3daf13ecd950a5567d813fb2e38aa1
https://pubmed.ncbi.nlm.nih.gov/23534532
https://pubmed.ncbi.nlm.nih.gov/23534532
Publikováno v:
British journal of haematology. 107(3)
A rapid, non-radioactive, PCR-based method to genotype the XbaI restriction fragment length polymorphism of the human factor VIII gene is described. The method uses long-distance PCR followed by XbaI restriction digestion and agarose gel electrophore
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::82636137de450b724d522023a2ae9116
https://pubmed.ncbi.nlm.nih.gov/10583260
https://pubmed.ncbi.nlm.nih.gov/10583260
Autor:
A F, Fundia, I B, Larripa
Publikováno v:
Acta physiologica, pharmacologica et therapeutica latinoamericana : organo de la Asociacion Latinoamericana de Ciencias Fisiologicas y [de] la Asociacion Latinoamericana de Farmacologia. 41(3)
Many human malignancies are thought to be caused in large part by environmental agents. Studies indicate that ionizing radiation and many chemical mutagens/carcinogens appear to induce chromosomal mutations. Recently, it was suggested that chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3afdda5bc89660fa200ffd54947b642
https://pubmed.ncbi.nlm.nih.gov/1843869
https://pubmed.ncbi.nlm.nih.gov/1843869
Publikováno v:
Sangre. 35(1)
Fragile sites are specific chromosomal sites prone to breakage and rearrangements and they are probably related with cancer development. Fragile sites expression induced by 5-fluorodeoxyuridine (FudR) or 5-bromodeoxyuridine (BrdU) was analyzed in 4 h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c0b256be6966276dabcd2905194da196
https://pubmed.ncbi.nlm.nih.gov/2139745
https://pubmed.ncbi.nlm.nih.gov/2139745
Autor:
I B, Larripa, S, Brieux de Salum
Publikováno v:
Sangre. 24(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d892614b48d1e6bcfc812e7f8455834d
https://pubmed.ncbi.nlm.nih.gov/314678
https://pubmed.ncbi.nlm.nih.gov/314678
Publikováno v:
Medicina. 48(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::99a425406636ed450f6f68614c81b722
https://pubmed.ncbi.nlm.nih.gov/3255038
https://pubmed.ncbi.nlm.nih.gov/3255038
Publikováno v:
Sangre. 34(6)
Bloom's syndrome (BS) is a rare autosomal recessive hereditary disorder associated with pre- and postnatal growth deficiency, a characteristic facial configuration, an increased risk of chromosome instability, and an increased risk of neoplasia. BS i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::95eef6d746f2b9d3ae4459203ac798c6
https://pubmed.ncbi.nlm.nih.gov/2629124
https://pubmed.ncbi.nlm.nih.gov/2629124
Autor:
S B, de Salum, I B, Larripa
Publikováno v:
Medicina. 38(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26e841843b26ad89fd06e901117c5115
https://pubmed.ncbi.nlm.nih.gov/362117
https://pubmed.ncbi.nlm.nih.gov/362117