Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Leopoldo A. García-Montaño"'
Autor:
Juan C. Zenteno, Leopoldo A. García‐Montaño, Marisa Cruz‐Aguilar, Josué Ronquillo, Agustín Rodas‐Serrano, Luis Aguilar‐Castul, Rodrigo Matsui, Carlos I. Vencedor‐Meraz, Rocío Arce‐González, Federico Graue‐Wiechers, Mario Gutiérrez‐Paz, Tatiana Urrea‐Victoria, Ulises deDios Cuadras, Oscar F. Chacón‐Camacho
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 1, Pp n/a-n/a (2020)
Abstract Background Retinal dystrophies (RDs) are one of the most genetically heterogeneous monogenic disorders with ~270 associated loci identified by early 2019. The recent application of next‐generation sequencing (NGS) has greatly improved the
Externí odkaz:
https://doaj.org/article/4e36894b39154203a322ba28354f0774
Autor:
Leopoldo A. García-Montaño, Yamhilette Licón-Muñoz, Frank J. Martinez, Yasine R. Keddari, Michael K. Ziemke, Muhammad O. Chohan, Sara G.M. Piccirillo
Publikováno v:
Molecular Cancer Research. :OF1-OF13
The treatment of the most aggressive primary brain tumor in adults, glioblastoma (GBM), is challenging due to its heterogeneous nature, invasive potential, and poor response to chemo- and radiotherapy. As a result, GBM inevitably recurs and only a fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d11e2a1555191f2ed6fa6c342eb08024
https://doi.org/10.1158/1541-7786.mcr-23-0048
https://doi.org/10.1158/1541-7786.mcr-23-0048
Autor:
Leopoldo A. García-Montaño, Yamhilette Licón Muñoz, Frank Martinez, Kandee Gallegos, Huining Kang, Sara G. Piccirillo
Publikováno v:
Cancer Research. 83:544-544
Glioblastoma (GBM) is the most common malignant brain tumor in adults and is characterized by heterogeneous nature, invasive potential, and poor treatment response. Work from The Cancer Genome Atlas (TCGA) has identified the tumor suppressor gene TP5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49be805810c937ea357f9e24d5f4f7fd
https://doi.org/10.1158/1538-7445.am2023-544
https://doi.org/10.1158/1538-7445.am2023-544
Autor:
José Dalma-Weiszhausz, Oscar Chacón-Camacho, Patricia CHEVEZ-BARRIOS, Juan C. Zenteno, Valentina Franco-Cárdenas, Leopoldo A. García-Montaño, Jehieli Pérez-Bravo, Iván A. García-Montalvo, Juan M. Jiménez-Sierra, Alexander Dalma
Publikováno v:
Retina (Philadelphia, Pa.). 42(5)
Autosomal dominant Müller cell dystrophy is a rare condition we described in 1991. It is characterized by a striking sheen appearance on the retinal surface with progressive retinal changes leading to disorganization and atrophy with a decreased b-w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5c2513fbb38e249ab4ee893953331cb
https://pubmed.ncbi.nlm.nih.gov/35125479
https://pubmed.ncbi.nlm.nih.gov/35125479
Autor:
Leopoldo A García-Montaño, Mirena C Astiazarán, Humberto Matiz-Moreno, Juan Carlos Zenteno, Francisco Sánchez-Moreno
Publikováno v:
American Journal of Medical Genetics Part A. 176:2637-2645
Congenital cataract (CC) is a significant cause of childhood blindness worldwide. CC is a genetically heterogeneous disease because mutations in over 40 genes have been demonstrated to cause the disorder and up to 40% of cases arise from single-gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::543570c74b480d3c62670d6276116ba2
https://doi.org/10.1002/ajmg.a.40524
https://doi.org/10.1002/ajmg.a.40524
Autor:
Carlos I Vencedor-Meraz, Rocio Arce-Gonzalez, Oscar F. Chacon-Camacho, Josue Ronquillo, Marisa Cruz-Aguilar, Agustín Rodas-Serrano, Leopoldo A García-Montaño, Ulises de Dios Cuadras, Luis Aguilar-Castul, Federico Graue-Wiechers, Rodrigo Matsui, Juan Carlos Zenteno, Mario Gutiérrez-Paz, Tatiana Urrea-Victoria
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 1, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Retinal dystrophies (RDs) are one of the most genetically heterogeneous monogenic disorders with ~270 associated loci identified by early 2019. The recent application of next‐generation sequencing (NGS) has greatly improved the molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9edbbcb5899db09b186ce6fce66f421d
https://doi.org/10.1002/mgg3.1044
https://doi.org/10.1002/mgg3.1044
Autor:
Carolina I. Galaz-Montoya, Sofia Alcaraz-Estrada, Leopoldo A. García-Montaño, Juan C. Zenteno, Raúl Piña-Aguilar
Publikováno v:
Boletín Médico del Hospital Infantil de México (English Edition). 76
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46bdb90e37e70056e5e823807cdc7e64
https://doi.org/10.24875/bmhime.m19000053
https://doi.org/10.24875/bmhime.m19000053
Autor:
Sofia L. Alcaraz-Estrada, Raul E. Piña-Aguilar, Leopoldo A García-Montaño, Carolina I. Galaz-Montoya, Juan Carlos Zenteno
Publikováno v:
Boletín Médico del Hospital Infantil de México. 76
Introduccion: Los trastornos pediatricos del movimiento representan un reto diagnostico para pediatras y neurologos pediatras debido a su gran heterogeneidad clinica y caracteristicas comunes compartidas. Por lo tanto, los diagnosticos especificos re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad62b43c9a5cd02b6abab9797ac1731c
https://doi.org/10.24875/bmhim.18000099
https://doi.org/10.24875/bmhim.18000099
Autor:
Iván Antonio García-Montalvo, Leopoldo A García-Montaño, Tania Barragán-Arévalo, Jessica Nava-Valdez, Cristina Villanueva-Mendoza, Marisa Cruz-Aguilar, Diana Matías-Pérez, Camilo E Villarroel, Clavel Guadarrama-Vallejo, Rocío Villafuerte-de la Cruz, Oscar F. Chacon-Camacho, Juan Carlos Zenteno
Publikováno v:
Journal of human genetics. 63(11)
Severe congenital eye malformations, particularly microphthalmia and anophthalmia, are one of the main causes of visual handicap worldwide. They can arise from multifactorial, chromosomal, or monogenic factors and can be associated with extensive cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a49c3a1320c1fbb1f907f84c9553acab
https://pubmed.ncbi.nlm.nih.gov/30181649
https://pubmed.ncbi.nlm.nih.gov/30181649
Publikováno v:
Expert review of molecular diagnostics. 17(11)
Retinal dystrophies (RDs) are the most common cause of inherited blindness and one of the most genetically heterogeneous human diseases. RDs arise from mutations in genes involved in development and function of photoreceptors or other retinal cells.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5fb5550e0d8ace29f5653b0672e4b5f
https://pubmed.ncbi.nlm.nih.gov/28945154
https://pubmed.ncbi.nlm.nih.gov/28945154