Výsledky vyhledávání - "Aurora Ibarra‐Arce"

Akademický článek

Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis

Autor: Aurora Ibarra‐Arce, Manuel Almaraz‐Salinas, Víctor Martínez‐Rosas, Gabriela Ortiz de Zárate‐Alarcón, Laura Flores‐Peña, Mirza Romero‐Valdovinos, Angélica Olivo‐Díaz

Publikováno v: Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)

Abstract Background Craniosynostosis is one of the major genetic disorders affecting 1 in 2,100–2,500 live newborn children. Environmental and genetic factors are involved in the manifestation of this disease. The suggested genetic causes of cranio

Externí odkaz: https://doaj.org/article/5201203379754ede87ee8603862f2ae3

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Association between cycle threshold ( C t ) values and clinical and laboratory data in inpatients with COVID‐19 and asymptomatic health workers

Publikováno v: Journal of Medical Virology. 93:5969-5976

In-house assays for the diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by quantitative reverse-transcription polymerase chain reaction (qRT-PCR), are feasible alternatives, particularly in developing countries. Cycle thresh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d33420add0b7a709135e23c06d84d5c6
https://doi.org/10.1002/jmv.27170

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Association between cycle threshold (C

Publikováno v: Journal of Medical Virology

In‐house assays for the diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) by quantitative reverse‐transcription polymerase chain reaction (qRT‐PCR), are feasible alternatives, particularly in developing countries. Cy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::708dd1bc212c040d8b49bfa4c55471b7
https://pubmed.ncbi.nlm.nih.gov/34196423

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Cervical lymph node tuberculosis and TNF, IL8, IL10, IL12B and IFNG polymorphisms

Autor: Olga, Plowes-Hernández, Héctor, Prado-Calleros, Sara, Arroyo-Escalante, Beatriz, Zavaleta-Villa, Javier, Flores-Osorio, Aurora, Ibarra Arce, Mirza, Romero-Valdovinos, Angélica, Olivo-Díaz

Publikováno v: The new microbiologica. 44(1)

Cervical lymph node tuberculosis (LNTB) is the most common manifestation of extrapulmonary tuberculosis, resulting from the interaction of environmental and genetic factors. The immune response against TB is regulated by several cytokines, which have

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a748f2f19f1f7379db1e3172c8cc25c2
https://pubmed.ncbi.nlm.nih.gov/33582825

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SARS-CoV-2 Identification in Saliva: Are We Interpreting the Results Correctly?

Autor: Ana Flisser, Mirza Romero-Valdovinos, Héctor Manuel Prado-Calleros, Angel Kaleb Romero-Gonzalez, Luz Elena Espinosa de los Monteros-Perez, Yunuen Rodriguez-Sanchez, Lourdes Suarez-Roa, Aurora Ibarra-Arce, Juan Pablo Ramirez-Hinojosa, Marisol Chavez-Gutierrez, Nelly Raquel Gonzalez-Arenas, Angélica Olivo-Díaz, Guillermina Avila-Ramirez, Rigoberto Hernández-Castro, Pablo Maravilla, Sara Arroyo-Escalante, Octavio Sierra-Martinez, Beatriz Zavaleta-Villa

BackgroundIn the present study, we obtained cycle threshold (Ct) values by qRT-PCR and compared them with clinical and laboratory data from saliva specimens of inpatients with COVID-19 and asymptomatic health workers (AHW).MethodsSaliva specimens fro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::13742733bf72f3af33cc347090c3a01d
https://doi.org/10.21203/rs.3.rs-96189/v1

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Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis

Autor: Angélica Olivo-Díaz, Mirza Romero-Valdovinos, Manuel Almaraz-Salinas, Laura Flores-Peña, Víctor Martínez-Rosas, Aurora Ibarra-Arce, Gabriela Ortiz de Zarate-Alarcón

Publikováno v: Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)

Background Craniosynostosis is one of the major genetic disorders affecting 1 in 2,100–2,500 live newborn children. Environmental and genetic factors are involved in the manifestation of this disease. The suggested genetic causes of craniosynostosi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c6ffd390dfda34f5312bf1244532c41
http://europepmc.org/articles/PMC7434736

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IRF6 polymorphisms in Mexican patients with non-syndromic cleft lip

Autor: Mirza Romero-Valdovinos, Martín García-Álvarez, Daniel Cortés-González, Sandra Sánchez-Camacho, Aurora Ibarra-Arce, Angélica Olivo-Díaz, Laura Flores-Peña, Gabriela Ortiz de Zarate-Alarcón, Silvia Arenas-Díaz

Publikováno v: Meta Gene

Cleft lip with or without cleft palate (CL/P) is one of the most common birth defects; it is a multifactorial disease affecting > 1/1,000 live births in Europe, and its etiology is largely unknown, although it is very likely genetic and environmental

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5c7db4321aa831c1e352b5c118934a3

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Mutations in the FGFR2 gene in Mexican patients with Apert syndrome

Autor: Laura Flores-Peña, Aurora Ibarra-Arce, Mirza Romero-Valdovinos, Angélica Olivo-Díaz, G. Ortiz de Zárate-Alarcón, F. Martínez-Hernández

Publikováno v: Genetics and molecular research : GMR. 14(1)

Apert syndrome (AS) is a frequent acrocephalosyndactyly, with autosomal dominant inheritance. AS has been associated with mutations in fibroblast growth factor receptor 2 (FGFR2), and approximately 99% of cases show 2 of the frequent mutations locate

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::974cd1aa27fda116901c1053ca233d24
https://pubmed.ncbi.nlm.nih.gov/25867380

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