Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mercedes Vázquez‐Cantú"'
Autor:
Laura Prochazka, Yale S Michaels, Charles Lau, Ross D Jones, Mona Siu, Ting Yin, Diana Wu, Esther Jang, Mercedes Vázquez‐Cantú, Penney M Gilbert, Himanshu Kaul, Yaakov Benenson, Peter W Zandstra
Publikováno v:
Molecular Systems Biology, Vol 18, Iss 11, Pp 1-22 (2022)
Abstract During development, cell state transitions are coordinated through changes in the identity of molecular regulators in a cell type‐ and dose‐specific manner. The ability to rationally engineer such transitions in human pluripotent stem ce
Externí odkaz:
https://doaj.org/article/e2b62297353c4d7b84600c9edd7e25df
Autor:
Consuelo Cantú-Reyna, Roberto Galindo-Ramírez, Mercedes Vázquez-Cantú, Lorenza Haddad-Talancón, Willebaldo García-Muñoz
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-7 (2021)
Abstract Background Cystic fibrosis (CF) is an autosomal recessive disorder caused by pathogenic variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The CF variants incidence is highly variable and even undetermined in so
Externí odkaz:
https://doaj.org/article/75ccd532496d47dfac545f8b9f09c288
Autor:
Consuelo Cantú-Reyna MD, Luis Manuel Zepeda MD, René Montemayor MD, Santiago Benavides MD, Héctor Javier González MD, Mercedes Vázquez-Cantú BS, Héctor Cruz-Camino BS
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 4 (2016)
Newborn screening for the detection of inborn errors of metabolism (IEM), endocrinopathies, hemoglobinopathies, and other disorders is a public health initiative aimed at identifying specific diseases in a timely manner. Mexico initiated newborn scre
Externí odkaz:
https://doaj.org/article/0c081410126447028c7cee72bcd92468
Autor:
Lorenza Haddad-Talancón, Willebaldo García-Muñoz, Mercedes Vázquez-Cantú, Consuelo Cantú-Reyna, Roberto Galindo-Ramírez
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-7 (2021)
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-7 (2021)
Background Cystic fibrosis (CF) is an autosomal recessive disorder caused by pathogenic variants in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The CF variants incidence is highly variable and even undetermined in some countr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09564a6bdca18b6c01f16c13a50058d4
https://pubmed.ncbi.nlm.nih.gov/34740355
https://pubmed.ncbi.nlm.nih.gov/34740355
Autor:
Héctor Cruz-Camino, Santiago Benavides, Héctor Javier González, Luis Manuel Zepeda, Consuelo Cantú-Reyna, Mercedes Vázquez-Cantú, René Montemayor
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Volume: 4, Article number: e150013, Published: 30 MAY 2019
Journal of Inborn Errors of Metabolism and Screening, Vol 4 (2016)
Journal of Inborn Errors of Metabolism and Screening v.4 2016
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Journal of Inborn Errors of Metabolism and Screening, Vol 4 (2016)
Journal of Inborn Errors of Metabolism and Screening v.4 2016
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Newborn screening for the detection of inborn errors of metabolism (IEM), endocrinopathies, hemoglobinopathies, and other disorders is a public health initiative aimed at identifying specific diseases in a timely manner. Mexico initiated newborn scre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03b2a95bc5446c4ca24d6db1181e94a6
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942016000100303&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2326-45942016000100303&lng=en&tlng=en
Autor:
Héctor Cruz-Camino, Jesús Santos-Guzmán, Consuelo Cantú-Reyna, Antonio Bandala-Jacques, Mercedes Vázquez-Cantú, René Gómez-Gutiérrez, Diana Laura Vazquez-Cantu
Publikováno v:
The American Journal of Case Reports
Case series Patients: — Final Diagnosis: Hereditary spastic paraplegia type 4 Symptoms: Progressive psychomotor deterioration • mixed seizure patterns • corneal opacity • dysostotic bones • limb spasticity with extensor plantar responses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2f52e9725c3dca15e06f558da93d0f3
http://europepmc.org/articles/PMC7249741
http://europepmc.org/articles/PMC7249741