Publications by authors named "Fernando Fernández-Ramírez"

15Publications

Identification of genomic copy number variations in lung benign metastasizing leiomyomatosis.

Authors:
Everardo Hernández-Plata Ana Claudia Velázquez-Wong Carmina Jiménez-Ramírez Fernando Fernández-Ramírez Luz María Galicia-Sánchez César Antonio Flores-García José Manuel Hernández-Hernández Haydeé Rosas-Vargas Juan Carlos Huicochea-Montiel Eliseo Espinosa-Poblano

Clin Respir J 2019 Feb 29;13(2):105-113. Epub 2019 Jan 29.

Servicio de Neumología, Unidad Médica de Alta Especialidad, Hospital de Especialidades del Centro Médico Nacional, Siglo XXI, IMSS, Ciudad de México, México.

View Article and Find Full Text PDF
February 2019

Trypanocidal and toxicological assessment in vitro and in silico of three sesquiterpene lactones from Asteraceae plant species.

Authors:
Omar Sepúlveda-Robles Bertha Espinoza-Gutiérrez Juan C Gomez-Verjan Silvia Laura Guzmán-Gutiérrez Marlon De Ita Mayra Silva-Miranda Clara Inés Espitia-Pinzón Fernando Fernández-Ramírez Alma Herrera-Salazar Minerva Mata-Rocha Alfredo Ortega-Hernández Ricardo Reyes-Chilpa

Food Chem Toxicol 2019 Mar 18;125:55-61. Epub 2018 Dec 18.

Instituto de Química, Universidad Nacional Autónoma de México, México. Electronic address:

View Article and Find Full Text PDF
March 2019

1799T>A Mutation Frequency in Mexican Mestizo Patients with Papillary Thyroid Cancer.

Authors:
Fernando Fernández-Ramírez Luis M Hurtado-López Mario A López Eva Martínez-Peñafiel Norma E Herrera-González Luis Kameyama Omar Sepúlveda-Robles

Biomed Res Int 2018 2;2018:2582179. Epub 2018 Apr 2.

Catedrático CONACyT, Unidad de Investigación Médica en Epidemiología Clínica, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, IMSS, Av. Cuauhtémoc 330, Cuauhtémoc, 06270 México City, Mexico.

View Article and Find Full Text PDF
October 2018

Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.

Authors:
Laura Gómez-Laguna Alejandro Martínez-Herrera Alejandra Del Pilar Reyes-de la Rosa Constanza García-Delgado Karem Nieto-Martínez Fernando Fernández-Ramírez Tania Yanet Valderrama-Atayupanqui Ariadna Berenice Morales-Jiménez Judith Villa-Morales Susana Kofman Alicia Cervantes Verónica Fabiola Morán-Barroso

Ophthalmic Genet 2018 Jan-Feb;39(1):56-62. Epub 2017 Sep 18.

c Department of Genetics , Hospital Infantil de México Federico Gómez , Mexico City , Mexico.

View Article and Find Full Text PDF
March 2018

Copy Number Alterations Associated with Acute Lymphoblastic Leukemia in Mexican Children. A report from The Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia.

Authors:
Beatriz Rosales-Rodríguez Fernando Fernández-Ramírez Juan Carlos Núñez-Enríquez Ana Claudia Velázquez-Wong Aurora Medina-Sansón Elva Jiménez-Hernández Janet Flores-Lujano José Gabriel Peñaloza-González Rosa Martha Espinosa-Elizondo María Luisa Pérez-Saldívar José Refugio Torres-Nava Jorge Alfonso Martín-Trejo Gabriela Bibiana Martínez-Morales Vilma Carolina Bekker-Méndez Juan Manuel Mejía-Aranguré Haydee Rosas-Vargas

Arch Med Res 2016 11;47(8):706-711

Unidad de Investigación Médica en Genética Humana, UMAE Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social (IMSS), Mexico City, Mexico. Electronic address:

View Article and Find Full Text PDF
November 2016

Congenital hypertrichosis universalis in Mexican female twins.

Authors:
Alicia Cervantes Constanza García-Delgado Fernando Fernández-Ramírez Adriana Valencia-Herrera Susana Kofman Verónica Morán-Barroso

Int J Dermatol 2016 Jan 30;55(1):e29-31. Epub 2015 Oct 30.

Department of Genetics, Hospital General de México Dr. Eduardo Liceaga, Mexico City, Mexico.

View Article and Find Full Text PDF
January 2016

Molecular Analysis by Gene Expression of Mitochondrial ATPase Subunits in Papillary Thyroid Cancer: Is ATP5E Transcript a Possible Early Tumor Marker?

Authors:
Luis Mauricio Hurtado-López Fernando Fernández-Ramírez Eva Martínez-Peñafiel José Damián Carrillo Ruiz Norma Estela Herrera González

Med Sci Monit 2015 Jun 16;21:1745-51. Epub 2015 Jun 16.

Molecular Oncology, Escuela Superior de Medicina, Instituto Politecnico Nacional, Mexico, Mexico.

View Article and Find Full Text PDF
June 2015

PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.

Authors:
Julián Nevado Jill A Rosenfeld Rocío Mena María Palomares-Bralo Elena Vallespín María Ángeles Mori Jair A Tenorio Karen W Gripp Elizabeth Denenberg Miguel Del Campo Alberto Plaja Rubén Martín-Arenas Fernando Santos-Simarro Lluis Armengol Gordon Gowans María Orera M Carmen Sanchez-Hombre Esther Corbacho-Fernández Alberto Fernández-Jaén Chad Haldeman-Englert Sulagna Saitta Holly Dubbs Duban B Bénédicte Xia Li Lani Devaney Mary Beth Dinulos Stephanie Vallee M Carmen Crespo Blanca Fernández Victoria E Fernández-Montaño Inmaculada Rueda-Arenas María Luisa de Torres Jay W Ellison Salmo Raskin Carlos A Venegas-Vega Fernando Fernández-Ramírez Alicia Delicado Sixto García-Miñaúr Pablo Lapunzina

Eur J Hum Genet 2015 Dec 8;23(12):1615-26. Epub 2015 Apr 8.

CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, ISCIII, Madrid, Spain.

View Article and Find Full Text PDF
December 2015

19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype.

Authors:
Carlos Venegas-Vega Karem Nieto-Martínez Alejandro Martínez-Herrera Laura Gómez-Laguna Jaime Berumen Alicia Cervantes Susana Kofman Fernando Fernández-Ramírez

Mol Cytogenet 2014 12;7(1):61. Epub 2014 Dec 12.

Unidad de Genética, Hospital General de México, Dr. Balmis 148, México, D.F 06726 México.

View Article and Find Full Text PDF
December 2014

Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.

Authors:
Alicia Cervantes Constanza García-Delgado Fernando Fernández-Ramírez Carolina Galaz-Montoya Ariadna Berenice Morales-Jiménez Karem Nieto-Martínez Laura Gómez-Laguna Judith Villa-Morales Mónica Quintana-Palma Jaime Berúmen Susana Kofman Verónica F Morán-Barroso

BMC Med Genomics 2014 Sep 15;7:55. Epub 2014 Sep 15.

Departamento de Genética, Hospital Infantil de México Federico Gómez, Calle Dr, Márquez 162, Col, Doctores, Del, Cuauhtémoc, 06720 México, D,F,, México.

View Article and Find Full Text PDF
September 2014

Diagnosis of familial Wolf-Hirschhorn syndrome due to a paternal cryptic chromosomal rearrangement by conventional and molecular cytogenetic techniques.

Authors:
Carlos A Venegas-Vega Fernando Fernández-Ramírez Luis M Zepeda Karem Nieto-Martínez Laura Gómez-Laguna Luz M Garduño-Zarazúa Jaime Berumen Susana Kofman Alicia Cervantes

Biomed Res Int 2013 3;2013:209204. Epub 2013 Feb 3.

Servicio de Genética, Hospital General de México, Dr. Balmis No. 148, Colonia Doctores, 06726 México, DF, Mexico.

View Article and Find Full Text PDF
September 2013

Overexpression of Ipe protein from the coliphage mEp021 induces pleiotropic effects involving haemolysis by HlyE-containing vesicles and cell death.

Authors:
Eva Martínez-Peñafiel Fernando Fernández-Ramírez Cecilia Ishida Ruth Reyes-Cortés Omar Sepúlveda-Robles Gabriel Guarneros-Peña Rosa María Bermúdez-Cruz Luis Kameyama

Biochimie 2012 Jun 18;94(6):1262-73. Epub 2012 Feb 18.

Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Av. Instituto Politécnico Nacional No. 2508, C.P. 07360, México D.F., Mexico.

View Article and Find Full Text PDF
June 2012

α-Enolase binds to RNA.

Authors:
Liliana Hernández-Pérez Francisco Depardón Fernando Fernández-Ramírez Alejandra Sánchez-Trujillo Rosa María Bermúdez-Crúz Lawrence Dangott Cecilia Montañez

Biochimie 2011 Sep 20;93(9):1520-8. Epub 2011 May 20.

Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del IPN., Avenida Instituto Politécnico Nacional 2508, Apartado postal 14-740, DF CP 07360, Mexico.

View Article and Find Full Text PDF
September 2011

Nucleic acid and protein factors involved in Escherichia coli polynucleotide phosphorylase function on RNA.

Authors:
Fernando Fernández-Ramírez Rosa M Bermúdez-Cruz Cecilia Montañez

Biochimie 2010 May 28;92(5):445-54. Epub 2010 Jan 28.

Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del IPN, DF, Mexico.

View Article and Find Full Text PDF
May 2010

Conserved domains in polynucleotide phosphorylase among eubacteria.

Authors:
Rosa María Bermúdez-Cruz Fernando Fernández-Ramírez Fernando Ramírez Luis Kameyama-Kawabe Cecilia Montañez

Biochimie 2005 Aug 8;87(8):737-45. Epub 2005 Apr 8.

Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del I.P.N., Apartado postal 14-740, D.F. C.P. 07360 Mexico, Mexico.

View Article and Find Full Text PDF
August 2005