Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Luciana Vasquez"'
Autor:
Ana Luiza Garcia Massaguer Millás, Juliana Lago, Luciana Vasquez-Pinto, Pedro Xavier Rodriguez Massaguer, Silvya Stuchi Maria-Engler
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
We are close to achieving the production of a biomimetic functional skin and this advance is mainly due to the demand that is not limited to the field of regenerative medicine, the need for transplantation of this organ due to the aging of the popula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::186aacf3b0fec90412ff80097fd72c2c
Autor:
Mayana Zatz, Tom Strachan, Anthea Stephenson, Luciana Vasquez, Ibrahim Mahneh, Katharine Bushby, Egbert Bakker, Sharon Keers, Eloisa de Sá Moreira, Suely Kazue Nagahashi Marie, M. Rita Passos-Bueno, Jean Weissenbach, Ramaisa Bashir, Mariz Vainzof, Paula Iughetti
Publikováno v:
Genomics. 27:192-195
The mild autosomal recessive limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of muscle diseases. The first gene to be mapped and associated with this phenotype was a locus on 15q based on linkage analysis in families from a French g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d991742d81dbe8b4f85950aa39d5dd9c
https://doi.org/10.1006/geno.1995.1024
https://doi.org/10.1006/geno.1995.1024
Autor:
Luciana Vasquez, Beny Lafer, M. Rita Passos-Bueno, Valentim Gentil, João Ricardo Mendes de Oliveira, Mayana Zatz, Paulo Alberto Otto, Homero Vallada, Helio Elkis, Valéria Lauriano
Publikováno v:
American Journal of Medical Genetics. 81:225-227
It has been suggested that the serotonin transporter (5-hydroxytryptamine-transporter or 5-HTT) may be involved in the pathogenesis of affective disorders. Recently, Collier et al. (1996) found that the frequency of the low-activity short variant (s)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e25cb22a30e0d105056b2b9cfdca936
https://doi.org/10.1002/(sici)1096-8628(19980508)81:3<225::aid-ajmg4>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19980508)81:3<225::aid-ajmg4>3.0.co
Autor:
Kate Bushby, R. Bashir, João Ricardo Mendes de Oliveira, Luciana Vasquez, Mayana Zatz, Suely Kazue Nagahashi Marie, Egbert Bakker, Eloisa de Sá Moreira, Donald R. Love, Mariz Vainzof, Maria Rita Passos-Bueno, Tom Strachan, Paula Iughetti
Publikováno v:
Scopus-Elsevier
Autosomal recessive limb-girdle muscular dystrophies (AR LGMD) represent a group of muscle diseases with a wide spectrum of clinical signs, varying from very severe to mild. Four different loci that when mutated cause the AR LGMD phenotype have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e82b5cb551626d54d484a0860c9ceba
https://pubmed.ncbi.nlm.nih.gov/8929943
https://pubmed.ncbi.nlm.nih.gov/8929943
Autor:
Raquel Ribeiro Gomes, Luciana Vasquez, Priscilla G. Otto, José Salomão Schwartzman, Mayana Zatz, Cintia Fridman, Célia Priszkulnik Koiffmann
Publikováno v:
The American Journal of Human Genetics. (6):1781-1784
The collaboration of Drs. Mariz Vainzof, Maria Rita Passos-Bueno, and Lygia V. Pereira and of Constancia Urbani is gratefully acknowledged. This research was supported with grants from the Fundacao de Amparo a Pesquisa do Estado de Sao Paulo, Program
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2c461a1669b521a6a42b5d60e8d4b56