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scopus(24)
The Hypothesis of the Prolonged Cell Cycle in Turner Syndrome
ReviewAbstract: Turner syndrome (TS) is a chromosomal disorder that is caused by a missing or structurally abnormalPalabras claves:cell proliferation, congenital heart disease, embryonic lethality, Folliculogenesis, neuropsychological profile, prolonged cell cycle, Short stature, Turner syndromeAutores:Francisco Álvarez-Nava, Soto-Quintana M.Fuentes:googlescopusUtility of chromosome banding with ALU I enzyme for identifying methylated areas in breast cancer
ArticleAbstract: Cancer is a group of disorders characterized by uncontrolled cell growth which is produced by two suPalabras claves:Breast Cancer, Chromosome banding, Methylation of DNA, Restriction enzymes ALU IAutores:Cañizález J., Francisco Álvarez-Nava, González R., Maribel Quintero, Quintero M., Raquel Atencio, Ricardo A.T., Rojas-Atencio A.E., Soto-Álvarez M., Urdaneta K., Yamarte L.Fuentes:googlescopusDiagnosis and management of patients with sex differentiation disorders: experience at the Unit of Medical Genetics of the University of Zulia, Maracaibo, Venezuela
ArticleAbstract: Abnormalities of sexual differentiation (ASD) represent a group of entities, heterogeneous in theirPalabras claves:Autores:Francisco Álvarez-Nava, González-Ferrer S., Soto-Quintana M.Fuentes:googlescopusDisminished zinc plasma concentrations and alterations in the number of lymphocyte subpopulations in Down's syndrome patients
ArticleAbstract: Alterations of plasma levels of zinc and in the immune system in Down's syndrome (DS) have been repoPalabras claves:Down syndrome, Lymphocyte subpopulations, ZincAutores:Fernández D., Francisco Álvarez-Nava, Fulcado W., Granadillo V., López E., Ocando A., Rojas-Atencio A.E., Soto-Quintana M.Fuentes:googlescopusGH/IGF-1 signaling and current knowledge of epigenetics; A review and considerations on possible therapeutic options
ReviewAbstract: Epigenetic mechanisms play an important role in the regulation of the Growth Hormone- Insulin-like GPalabras claves:Epigenetic drugs, Epigenetics, Gene regulation, Growth hormone, Insulin-like growth factor I, Intrauterine growth retardation, metabolism, Postnatal growthAutores:Francisco Álvarez-Nava, Lanes R.Fuentes:googlescopusGHR and VDR genes do not contribute to the growth hormone (GH) response in GH deficient and turner syndrome patients
ArticleAbstract: We have prospectively assessed the influence of GHR and VDR gene polymorphisms on the response to rhPalabras claves:GHR and VDR polymorphisms, Growth hormone deficiency, Growth hormone therapy, Turner syndromeAutores:Francisco Álvarez-Nava, Gunczler P., Lanes R., Marcano H., Paoli M., Pardo T., Soto-Quintana M., Villalobos J.Fuentes:googlescopusElevated second-trimester maternal serum β-human chorionic gonadotropin and amniotic fluid alpha-fetoprotein as indicators of adverse obstetric outcomes in fetal Turner syndrome
ArticleAbstract: Aim The objective of this study was to determine the ability of biochemical analytes to identify advPalabras claves:adverse pregnancy outcome, biochemical screening, Prenatal diagnosis, Turner syndromeAutores:Bracho A., Francisco Álvarez-Nava, Lanes R., Morales-Machin A., Pons H., Soto M.Fuentes:googlescopusEpigenetics in Turner syndrome
ReviewAbstract: Background: Monosomy of the X chromosome is the most frequent genetic abnormality in human as it isPalabras claves:Aneuploidy, Chromatin, DNA methylation, Embryonic stem cells, Epigenetics, gene expression, Mouse models, Turner syndromeAutores:Francisco Álvarez-Nava, Lanes R.Fuentes:googlescopusClonal chromosome abnormalities in malignant hematological diseases using fluorescence in situ hybridization
ArticleAbstract: Fluorescent in situ hybridization (FISH) is a rapid, sensitive and reliable method for the identificPalabras claves:Autores:Chirino H., Francisco Álvarez-Nava, González R., González-Ferrer S., Pineda-Del Villar L., Rojas-Atencio A.E., Soto-Quintana M., Urdaneta K.Fuentes:googlescopusComplete androgen insensitivity syndrome: Clinical and anatomopathological findings in 23 patients
ArticleAbstract: Complete Androgen Insensitivity Syndrome (CAIS) is a type of Male Pseudohermaphroditism due to a defPalabras claves:androgen receptor, Male pseudohermaphroditism, primary amenorrhea, Testicular feminization, Testicular tissueAutores:Francisco Álvarez-Nava, González S., Martinez C., Prieto-Carrasquero M., Soto-Quintana M.Fuentes:googlescopus