Nurgulsim, Kaster;
Abbas Raza, Sayed Haidar;
Khan, Rajwali;
Ali Shah, Mujahid;
Jahejo Ali, Raza;
Batool, Uzma;
Hongbao, Wang;
Nurlybai Zhigerbayevich, Kazhgaliev;
Schreurs, Nicola;
Zan, Linsen.
BACKGROUND: This study aimed to explore genetic polymorphisms of the CCKAR gene and their relationship with the growth and development of Qinchuan cattle which could be used as molecular markers for the improvement of the breeding of Qinchuan cattle. RESULTS: Here, we have identified seven single nucleot...
Bovinos/genética,
Productos de la Carne,
Ganado,
Polimorfismo de Nucleótido Simple,
Receptor de Colecistoquinina A/genética,
Variación Genética,
Sistema Digestivo,
Reacción en Cadena de la Polimerasa/métodos,
Técnicas de Genotipaje,
Frecuencia de los Genes,
Desequilibrio de Ligamiento
Guo, Xian;
Zhang, Sihuan;
Yang, Han;
Pei, Jie;
Wu, Xiaoyun;
Bao, Pengjia;
Liang, Chunnian;
Xiong, Lin;
Chu, Min;
Lan, Xianyong;
Yan, Ping.
BACKGROUND: Transmembrane protein 95 (TMEM95) plays a role in male fertility. Previous studies showed that genes with a significant impact on reproductive traits can also affect the growth traits of livestock. Thus, we speculated that the genetic variation of TMEM95 gene may have effects on growth traits...
Pacheco-Romero, José;
Acosta, Oscar;
Huerta, Doris;
Cabrera, Santiago;
Vargas, Marlene;
Mascaro, Pedro;
Huamán, Moisés;
Sandoval, José;
López, Rudy;
Mateus, Julio;
Gil, Enrique;
Guevara, Enrique;
Butrica, Nitza;
Catari, Diana;
Bellido, David;
Custodio, Gina;
Naranjo, Andrea.
Abstract Background: Preeclampsia is a multiorgan disorder associated with maternal and perinatal morbi-mortality. In Peru, incidence is 10% and accounts for 22% of maternal deaths. Genome and genetic epidemiological studies have found an association between preeclampsia and genetic polymorphisms. Obj...
Preeclampsia,
Estudios de Casos y Controles,
Frecuencia de los Genes,
Marcadores Genéticos,
Predisposición Genética a la Enfermedad,
Genotipo,
Perú/epidemiología,
Polimorfismo de Nucleótido Simple,
Preeclampsia/epidemiología,
Preeclampsia/genética,
Factor A de Crecimiento Endotelial Vascular/genética
Abstract The aim of this study was to estimate allelic and genotypic frequencies of markers in the leptin (LEP), pituitary transcription factor (PIT-1) and luteinizing hormone receptor (LHR) genes and evaluate their effects on reproductive traits and milk yield of Holstein cattle. Data from 147 cows from...
ABSTRACT Objective: We aimed to investigate the role of DIO2 polymorphisms rs225014 and rs12885300 in Graves' disease patients, mainly for controlling body weight following treatment. Subjects and methods: We genotyped 280 GD patients by the time of diagnosis and 297 healthy control individuals using a...
RESUMEN: El objetivo de este estudio fue describir la frecuencia genotípica y alélica del ACTN3 R577X y ECA I/D en atletas ciegos de fútbol 5. Se incluyó una metodología descriptiva con una muestra de 63 deportistas ciegos (28,0±5,8 años), todos varones, de equipos de fútbol 5 de alto rendimiento...
SUMMARY OBJECTIVE: The relationship between the clinicopathological and sociodemographics characteristics of acral melanomas diagnosed at BACKGROUND: This study aimed to investigate the frequency of VEGF gene insertion (I) / deletion (D) polymorphism (rs35569394) in patients with Polycystic Ovarian Synd...
The frequencies of the Human leukocyte antigen (HLA) alleles in the Puyanawa indigenous reserve population and their association with the NDO-LID and ELISA PGL-1 rapid serological test was assessed. This was a cross-sectional study with an epidemiological clinical design conducted in two indigenous commu...
Abstract Background: Alopecia areata is an autoimmune disease that produces non-scarring hair loss around the body. Gene variants of the cytotoxic T-lymphocyte antigen 4 (CTLA4) gene, a negative regulator of T-cell response, have been associated with a predisposition to autoimmune diseases in different ...
Alopecia Areata/genética,
Antígeno CTLA-4/genética,
Estudios de Casos y Controles,
Frecuencia de los Genes,
Estudios de Asociación Genética,
Predisposición Genética a la Enfermedad,
Variación Genética/genética,
Técnicas de Genotipaje,
México,
Persona de Mediana Edad,
Polimorfismo de Nucleótido Simple,
Factores de Riesgo
ABSTRACT Objective Type 1 diabetes mellitus (T1DM) is an autoimmune disorder caused by a complex interaction between environmental and genetic risk factors. BTB domain and CNC homolog 2 (BACH2) gene encodes a transcription factor that acts on the differentiation and formation of B and T lymphocytes. BA...
Factores de Transcripción con Cremalleras de Leucina de Carácter Básico/genética,
Brasil,
Estudios de Casos y Controles,
Diabetes Mellitus Tipo 1/genética,
Frecuencia de los Genes,
Predisposición Genética a la Enfermedad,
Genotipo,
Persona de Mediana Edad,
Reacción en Cadena de la Polimerasa,
Polimorfismo de Nucleótido Simple/genética,
Factores de Riesgo
