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pro vyhledávání: '"Santos, Manuella Maria Silva"'
Autor:
SANTOS, Manuella Maria Silva
Publikováno v:
Repositório Institucional da UFPEUniversidade Federal de PernambucoUFPE.
Submitted by Amanda Silva (amanda.osilva2@ufpe.br) on 2015-03-13T14:59:49Z No. of bitstreams: 2 DISSERTAÇÃO Manuella Maria Santos.pdf: 1230878 bytes, checksum: 21854ded68897cc54173c33b85cc9f42 (MD5) license_rdf: 1232 bytes, checksum: 66e71c371cc565
Externí odkaz:
https://repositorio.ufpe.br/handle/123456789/12493
Autor:
Santos, Manuella Maria Silva, Gatica, Damián, de Azêvedo Silva, Jaqueline, Crovella, Sergio, Klionsky, Daniel J., De Morais Jr, Marcos Antonio
Publikováno v:
In BBA - Molecular Basis of Disease 1 April 2021 1867(4)
Autor:
Xavier, Mariana Rodrigues, Santos, Manuella Maria Silva, Queiroz, Maise Gomes, de Lima Silva, Mariza S., Goes, Alexandre José S., De Morais Jr, Marcos Antonio
Publikováno v:
Molecular Biology Reports; Feb2020, Vol. 47 Issue 2, p1173-1185, 13p
Autor:
Santos, Manuella Maria Silva, De Morais, Marcos Antonio, Elsztein, Carolina, De Souza, Rafael Barros, Silva, Jaqueline Azevêdo, Crovella, Sergio, Paiva, Sérgio de Sá Leitão
Publikováno v:
Current Genetics; Aug2018, Vol. 64 Issue 4, p871-881, 11p
Autor:
Sérgio de Sá Leitão Paiva, Sergio Crovella, Carolina Elsztein, Jaqueline de Azevêdo Silva, Manuella Maria Silva Santos, Marcos Antonio de Morais, Rafael Barros de Souza
Mevalonate kinase deficiency (MKD) an orphan drug rare disease affecting humans with different clinical presentations, is still lacking information about its pathogenesis; no animal or cell model mimicking the genetic defect, mutations at MVK gene, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::648f83893276f4a4928a8a9803031512
http://hdl.handle.net/11368/2921122
http://hdl.handle.net/11368/2921122
Autor:
Jaqueline de Azevêdo Silva, Zilma Pereira Dos Anjosa, Sergio Crovella, Glaucia Alyne Nunes De Lacerda, Rafael Lima Guimarães, Manuella Maria Silva Santos, Lucas André Cavalcanti Brandão, J. Araujo, Natassia Javorski Rodrigues, N. A. C. Tavares
Ficolins are innate immune proteins able to activate the complement system by the lectin pathway. Single nucleotide polymorphisms (SNPs) of FCN1 and FCN2 genes, encoding for ficolin 1 and 2, have been related to the susceptibility to infectious and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c91c6717cf0234d79ca6a1fb7762b5fc
https://hdl.handle.net/11368/2893988
https://hdl.handle.net/11368/2893988
Autor:
Anjosa ZP; Department of Pathology, Federal University of Pernambuco, Recife, Pernambuco 50670-901 Brazil. crovelser@gmail.com., Santos MM, Rodrigues NJ, Lacerda GA, Araujo J, Silva JA, Tavares NA, Guimarães RL, Crovella S, Brandão LA
Publikováno v:
Journal of genetics [J Genet] 2016 Dec; Vol. 95 (4), pp. 1031-1034.