Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Thiago Donizete da Silva José"'
Autor:
Bárbara Amélia Santana-Lemos, Ana Paula Alencar de Lima Lange, Mariana Tereza de Lira Benício, Thiago Donizete da Silva José, Antônio Roberto Lucena-Araújo, Alexandre Krause, Carolina Hassibe Thomé, Eduardo Magalhães Rego
Publikováno v:
Haematologica, Vol 96, Iss 4 (2011)
Impairment of CCAAT Enhancer Binding Protein alpha (CEBPA) function is a common finding in acute myeloid leukemia; nevertheless, its relevance for acute promyelocytic leukemia pathogenesis is unclear. We analyzed the expression and assessed the methy
Externí odkaz:
https://doaj.org/article/b116c05e3e2649c8af0fd7abdb2b7819
Autor:
Sandra del Carmen Mendoza-Ruvalcaba, Aniel Jessica Leticia Brambila-Tapia, Jesús Alejandro Juárez-Osuna, Thiago Donizete Da Silva-José, José Elías García-Ortiz
Publikováno v:
Genetics and Molecular Biology, Vol 43, Iss 1 (2020)
Abstract Mucopolysaccharidoses (MPS) are a group of genetic disorders, each resulting from the deficiency of one of the lysosomal enzymes that catabolizes mucopolysaccharides. For the accurate diagnosis of the disease, the quantification of a specifi
Externí odkaz:
https://doaj.org/article/9164480da07b4466a4a9a202ec2c4754
Publikováno v:
Revista Biomédica. 32:147-160
Los biomarcadores son una herramienta importante en el diagnóstico, seguimiento y evaluación de la respuesta al tratamiento en pacientes con enfermedad de Gaucher (EG). El presente trabajo tiene como objetivo una revisión bibliográfica descriptiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d74810818660acfcf74ae9d3f24ca8e
https://doi.org/10.32776/revbiomed.v32i3.903
https://doi.org/10.32776/revbiomed.v32i3.903
Autor:
Thiago Donizete Da Silva-José, Jesús Alejandro Juárez-Osuna, Sandra C. Mendoza-Ruvalcaba, Angela Porras-Dorantes, José Elías García-Ortiz
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Background Metachromatic Leukodystrophy (MLD, OMIM 250100) is a neurodegenerative disease caused by mutations in the ARSA gene (OMIM 607574) that lead to deficiency in Arylsulfatase A (ASA). ASA pseudodeficiency (PD‐ASA) is a biochemical condition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c616c9a5165ceed93735f80d08d699b
https://doi.org/10.1002/mgg3.1305
https://doi.org/10.1002/mgg3.1305
Autor:
Thiago Donizete Da Silva-José, Angela Porras-Dorantes, Aniel Jessica Leticia Brambila-Tapia, José Elías García-Ortiz, Jesús Alejandro Juárez-Osuna, Alma Benita Lazcano-Castellanos
Publikováno v:
Journal of assisted reproduction and genetics. 34(10)
Recurrent spontaneous abortion (RSA) is a multifactorial condition that occurs with a frequency of 0.2-5% in women of reproductive age. Among genetic factors, the single nucleotide polymorphism (SNP) G1733A in the androgen receptor (AR) gene has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22c5e522197ae6549aba422a79777b59
https://pubmed.ncbi.nlm.nih.gov/29047007
https://pubmed.ncbi.nlm.nih.gov/29047007
Autor:
Thiago Donizete Da Silva-José, Alma Benita Lazcano-Castellanos, José Elías García-Ortiz, Aniel Jessica Leticia Brambila-Tapia, Angela Porras-Dorantes, Jesús Alejandro Juárez-Osuna
Publikováno v:
Journal of Assisted Reproduction and Genetics. 35:187-187
The original version of this article unfortunately contained two mistakes in the Abstract and the Discussion sections that the authors would like to correct.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aaa194fed7e8f93fe75073cce9f0515
https://doi.org/10.1007/s10815-017-1067-3
https://doi.org/10.1007/s10815-017-1067-3
Autor:
José Elías García-Ortiz, Sandra C. Mendoza-Ruvalcaba, Thiago Donizete Da Silva-José, Jesús Alejandro Juárez-Osuna
Publikováno v:
Molecular Genetics and Metabolism. 114:S44-S45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb90f9d7af4554fb7ce146f9a40cb5bc
https://doi.org/10.1016/j.ymgme.2014.12.085
https://doi.org/10.1016/j.ymgme.2014.12.085
Autor:
Sandra del Carmen Mendoza Ruvalcaba, Jesús Alejandro Juárez-Osuna, Thiago Donizete Da Silva-José, Angela Porras-Dorantes, José Elías García-Ortiz
Publikováno v:
Molecular Genetics and Metabolism. 117:S48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b51b66a72c89fc79c9350d648822273
https://doi.org/10.1016/j.ymgme.2015.12.263
https://doi.org/10.1016/j.ymgme.2015.12.263
Autor:
Antonio R. Lucena-Araujo, Eduardo Magalhães Rego, Carolina Hassibe Thomé, Barbara A. Santana-Lemos, Ana Paula Alencar de Lima Lange, Mariana Tereza Lira Benício, Thiago Donizete da Silva José, Alexandre Krause
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
Impairment of CCAAT Enhancer Binding Protein alpha (CEBPA) function is a common finding in acute myeloid leukemia; nevertheless, its relevance for acute promyelocytic leukemia pathogenesis is unclear. We analyzed the expression and assessed the methy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d10ee802004a5d04c4893a955ff7617
https://pubmed.ncbi.nlm.nih.gov/21134977
https://pubmed.ncbi.nlm.nih.gov/21134977