Zobrazeno 1 - 10
of 16
pro vyhledávání: '"E. A. Rebollar"'
Autor:
S. Ramírez-Barahona, F. M. González-Serrano, E. Martínez-Ugalde, A. Soto-Pozos, G. Parra-Olea, E. A. Rebollar
Publikováno v:
Animal Microbiome, Vol 5, Iss 1, Pp 1-13 (2023)
Abstract The composition and diversity of animal-associated microbial communities are shaped by multiple ecological and evolutionary processes acting at different spatial and temporal scales. Skin microbiomes are thought to be strongly influenced by
Externí odkaz:
https://doaj.org/article/afbe3aea01d54e9aa64df4bc09977528
Autor:
A. Martínez-Hernández, D. Martínez-Anaya, C. Durán-McKinster, V. Del Castillo-Ruiz, P. Navarrete-Meneses, E. J. Córdova, B. E. Villegas-Torres, A. Ruiz-Herrera, R. Juárez-Velázquez, E. Yokoyama-Rebollar, D. Cervantes-Barragán, A. Pedraza-Meléndez, L. Orozco, P. Pérez-Vera, C. Salas-Labadía
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-11 (2022)
Abstract Background To date, only twenty-one cases diagnosed postnatally with mosaic trisomy 12 have been reported. The most frequent phenotypic manifestations are developmental delay, dysmorphic facial features, congenital heart defects, digital alt
Externí odkaz:
https://doaj.org/article/0c4863867a0d412793d8ded32d6ea797
Autor:
C. Salas-Labadía, S. Gómez-Carmona, R. Cruz-Alcívar, D. Martínez-Anaya, V. Del Castillo-Ruiz, C. Durán-McKinster, V. Ulloa-Avilés, E. Yokoyama-Rebollar, A. Ruiz-Herrera, P. Navarrete-Meneses, E. Lieberman-Hernández, A. González-Del Angel, D. Cervantes-Barragán, C. Villarroel-Cortés, A. Reyes-León, D. Suárez-Pérez, A. Pedraza-Meléndez, A. González-Orsuna, P. Pérez-Vera
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Abstract Background Pigmentary mosaicism constitutes a heterogeneous group of skin pigmentation alterations associated with multisystem involvement. The aim of this study was to establish a complete cytogenetic and molecular characterization of PM pa
Externí odkaz:
https://doaj.org/article/3f654e9d49a44d4795a0f54cee82e329
Publikováno v:
Acta Pediátrica de México, Vol 37, Iss 5, Pp 289-296 (2016)
El síndrome de Down es la cromosomopatía más común del ser humano, con una frecuencia de 1 en 650 recién nacidos vivos. Las manifestaciones clínicas son muy variables y dependen, en gran parte, de la presencia de diversos factores genéticos co
Externí odkaz:
https://doaj.org/article/8f0e2be620cd4b7f931b22e499553186
Autor:
AR Vázquez del Campo, L Torres Maldonado, S Sánchez-Sandoval, S Frías Vázquez, E Lieberman Hernández, V del Castillo Ruiz, E Yokoyama Rebollar
Publikováno v:
Acta Pediátrica de México, Vol 37, Iss 5, Pp 271-281 (2016)
La duplicación de la región 5q34q35.3 se ha asociado a un fenotipo inverso de síndrome de Sotos, por contener el gen NSD1 en doble dosis. Se presenta a una paciente con retraso global del desarrollo, peso y talla bajos y dismorfias. Cuenta con ant
Externí odkaz:
https://doaj.org/article/87ffc3615feb4b6da309ac225b815485
Autor:
M A Cevallos, M D Basanta, E Bello-López, A S Escobedo-Muñoz, F M González-Serrano, A Nemec, Y J Romero-Contreras, M Serrano, E A Rebollar
Publikováno v:
FEMS Microbiology Ecology. 98
Chytridiomycosis, a lethal fungal disease caused by Batrachochytrium dendrobatidis (Bd), is responsible for population declines and extinctions of amphibians worldwide. However, not all amphibian species are equally susceptible to the disease; some s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::734f1b8b2b4dab2eaba72c9575cf14a8
https://doi.org/10.1093/femsec/fiac126
https://doi.org/10.1093/femsec/fiac126
Autor:
M. D. Basanta, S. L. Anaya‐Morales, E. Martínez‐Ugalde, T. M. González Martínez, V. D. Ávila‐Akerberg, M. V. Trejo, E. A. Rebollar
Publikováno v:
Animal Conservation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::430dd3c9aa2c2a255556a7290afb22f4
https://doi.org/10.1111/acv.12824
https://doi.org/10.1111/acv.12824
Autor:
C. Salas-Labadía, S. Gómez-Carmona, R. Cruz-Alcívar, D. Martínez-Anaya, V. Castillo-Ruiz, C. Durán-McKinster, V. Ulloa-Avilés, E. Yokoyama-Rebollar, A. Ruiz-Herrera, P. Navarrete-Meneses, E. Lieberman-Hernández, A. González-Del Angel, D. Cervantes-Barragán, C. Villarroel-Cortés, A. Reyes-León, D. Suárez-Pérez, A. Pedraza-Meléndez, A. González-Orsuna, P. Pérez-Vera
Additional file 1. “Cytogenetic alterations and molecular analysis detailed description”. The detailed descriptions of the abnormal karyotypes and molecular analysis in association with phenotype in 24 patients with chromosomal abnormalities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aae7b9ec22fdca2e539f81b055c4fc05
Clinal variation in Pinus hartwegii populations and its application for adaptation to climate change
Autor:
E. Loya-Rebollar, Roberto Lindig-Cisneros, J. A. Villegas-Moreno, N. M. Sánchez-Vargas, Cuauhtémoc Sáenz-Romero, Philippe Lobit
Publikováno v:
Silvae Genetica. 62:86-95
In order to determine the genetic variation among populations of Pinus hartwegii along altitudinal gradients, and the possible adaptive decoupling due to climatic change, a common garden test was set up with 13 provenances collected along an altitudi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce8b3dab79987648362837dbcd2125ec
https://doi.org/10.1515/sg-2013-0011
https://doi.org/10.1515/sg-2013-0011
Autor:
E Lieberman Hernández, L Torres Maldonado, E Yokoyama Rebollar, AR Vázquez del Campo, S Frías Vázquez, S Sánchez-Sandoval, V del Castillo Ruiz
Publikováno v:
Acta Pediátrica de México, Vol 37, Iss 5, Pp 271-281 (2016)
La duplicación de la región 5q34q35.3 se ha asociado a un fenotipo inverso de síndrome de Sotos, por contener el gen NSD1 en doble dosis. Se presenta a una paciente con retraso global del desarrollo, peso y talla bajos y dismorfias. Cuenta con ant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e86c2715eae5325092602e37a2deb476
https://doi.org/10.18233/apm37no5pp271-281
https://doi.org/10.18233/apm37no5pp271-281