Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Emiy Yokoyama-Rebollar"'
Autor:
Daniel Adrian Landero-Huerta, Rosa María Vigueras-Villaseñor, Emiy Yokoyama-Rebollar, Fabiola García-Andrade, Julio César Rojas-Castañeda, Luis Alonso Herrera-Montalvo, José Díaz-Chávez, Isidro Xavier Pérez-Añorve, Elena Aréchaga-Ocampo, Margarita Dolores Chávez-Saldaña
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Allelic variants in genes implicated in the development of testicular germ cell tumor (TGCT) could be present in patients with cryptorchidism (CO). Currently; the mechanisms explaining this relationship are still unknown. In this study the common cli
Externí odkaz:
https://doaj.org/article/09297e19c01b47c88341378f69000897
Publikováno v:
Acta Pediátrica de México, Vol 38, Iss 6, Pp 433-441 (2017)
La discapacidad intelectual (DI) o retraso mental tiene una prevalencia del 2-3% en la población general y se define como una alteración del neurodesarrollo que inicia antes de los 18 años. Se caracteriza por limitación importante en el funcionam
Externí odkaz:
https://doaj.org/article/57feefeb5a434ec8b238558f382d534c
Autor:
Jorge Román Corona-Rivera, Juan Carlos Zenteno, Leopoldo Gildardo López-Pérez, Emiy Yokoyama-Rebollar, Camilo E. Villarroel, Tania Barragán-Arévalo, Luis Ángel Montes-Almanza, Luz Consuelo Zepeda-Romero, Guadalupe Elena Morales-Domínguez, Christian Peña-Padilla, Lucina Bobadilla-Morales, Alfredo Corona-Rivera
Publikováno v:
Molecular Syndromology. 14:143-151
Introduction: PACS1-related neurodevelopmental disorder (PACS1-related NDD) is caused by pathogenic variants in the PACS1 gene and is characterized by a distinctive facial appearance, intellectual disability, speech delay, seizures, feeding difficult
Autor:
Eduardo Carrillo-Tapia, Sara E. Espinosa-Padilla, Daniela Perez-Perez, Maria E. Gonzalez-Serrano, Laura Berron-Ruiz, Francisco J. Espinosa-Rosales, Juan C. Rodriguez-Alba, Fabiola Mújica-Guzman, Emiy Yokoyama-Rebollar, Jose R. García-Flores, Norma E. Herrera-González, Selma Scheffler-Mendoza, Marco A. Yamazaki-Nakashimada, A. Tamara Staines-Boone, Gabriela Lopez-Herrera
Publikováno v:
Genetic testing and molecular biomarkers. 26(4)
Autor:
Roberto Cruz-Alcívar, P. Navarrete-Meneses, A. Reyes-León, A. González-Del Angel, V. Ulloa-Avilés, Patricia Pérez-Vera, A. I. Pedraza-Meléndez, A. González-Orsuna, S. Gómez-Carmona, Consuelo Salas-Labadía, David E. Cervantes-Barragán, Emiy Yokoyama-Rebollar, Esther Lieberman-Hernández, Adriana Ruiz-Herrera, Carola Durán-McKinster, D. Martínez-Anaya, V. Del Castillo-Ruiz, D. Suárez-Pérez, C. Villarroel-Cortés
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
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 patients, e
Autor:
Daniel Adrian Landero-Huerta, José Díaz-Chávez, Margarita Chávez-Saldaña, Luis A. Herrera, Emiy Yokoyama-Rebollar, Lucia Taja-Chayeb, Elena Aréchaga-Ocampo, Fabiola García-Andrade, Rosa María Vigueras-Villaseñor
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 34(7)
Objectives Cryptorchidism is the most common genitourinary birth defect in live newborn males and is considered as an important risk factor for testicular germ cell tumors and infertility. The Androgen Receptor gene is important in this pathology due
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
Autor:
Rosa María Vigueras-Villaseñor, Julio César Rojas-Castañeda, Elena Aréchaga-Ocampo, Margarita Chávez-Saldaña, Francisco Jimenez-Trejo, Emiy Yokoyama-Rebollar, Daniel Adrian Landero-Huerta
Publikováno v:
Frontiers in bioscience (Landmark edition). 22(7)
Testicular germ cell cancer (TGCT) is the most common malignancy among young adult males, which has become important due to its increased incidence and mortality in the population worldwide. The etiology is multifactorial. Recent studies have shown s
Publikováno v:
Acta Pediátrica de México. 40:44
El término artrogriposis (arthro = articulación; gryp = curva), también conocido como artrogriposis múltiple congénita o contracturas articulares congénitas múltiples, lo describió por primera vez (1841) Otto, como una miodistrofia.1 Se carac
Autor:
Silvia Sánchez-Sandoval, Emiy Yokoyama-Rebollar, Victoria Del Castillo-Ruiz, José Luis Castrillo, Silvia M Ávila-Flores, Adriana Ruiz-Herrera, Esther Lieberman-Hernández
Publikováno v:
Molecular Cytogenetics
Background The 15q11q13 region is subject to imprinting and is involved in various structural rearrangements. Less than 1% of Angelman Syndrome patients are due to translocations involving 15q11q13. These translocations can arise de novo or result fr