[PDF][PDF] DIVISIÓN DE ESTUDIOS DE POSTGRADO E INVESTIGACIÓN HOSPITAL GENERAL" DR. MANUEL GEA GONZÁLEZ
RSYRS DEL GEN - 2022 - ru.dgb.unam.mx
UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO FACULTAD DE MEDICINA DIVISIÓN DE
ESTUDIOS DE POSTGRADO E INVESTIGACIÓN HOSPITAL GENE Page 1 UNIVERSIDAD …
ESTUDIOS DE POSTGRADO E INVESTIGACIÓN HOSPITAL GENE Page 1 UNIVERSIDAD …
[HTML][HTML] Report of new haplotype for ABCC2 gene: rs17222723 and rs8187718 in cis
VM Pratt, BN Beyer, DL Koller, TC Skaar… - The Journal of Molecular …, 2015 - Elsevier
The ATP-binding cassette, subfamily C [CFTR/MRP], member 2 (ABCC2) gene is a member
of the ATP-binding cassette transporters and is involved in the transport of molecules across …
of the ATP-binding cassette transporters and is involved in the transport of molecules across …
Association of the ABCA1 gene polymorphisms with type 2 DM in a Japanese population
M Daimon, T Kido, M Baba, T Oizumi, Y Jimbu… - Biochemical and …, 2005 - Elsevier
To examine the association of the ATP-binding cassette transporter 1 (ABCA1) gene with
type 2 diabetes (DM), we studied genetic polymorphisms of the ABCA1 gene including its …
type 2 diabetes (DM), we studied genetic polymorphisms of the ABCA1 gene including its …
[HTML][HTML] Investigation Of C49620t Polymorphism In Abcc8 Gene In Patients With Type 2 Diabetes In The East Azerbaijan
S Joudi Shahabad, H Soltanzade… - Studies in Medical …, 2021 - umj.umsu.ac.ir
Background & Aims: Type 2 diabetes is a chronic disease that threatens public health. The
disease is on the rise with high complications worldwide. The C49620T variant of the …
disease is on the rise with high complications worldwide. The C49620T variant of the …
Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population
Background The association between ABCC8 gene C49620T polymorphism and type 2
diabetes (T2D) in populations of diverse ethnic backgrounds has been reported. However …
diabetes (T2D) in populations of diverse ethnic backgrounds has been reported. However …
Determinación de las frecuencias alélicas y genotípicas de 8 variantes en los genes DCK, CDA, ABCB1, GSTT1 y GSTM1 en una muestra de población colombiana …
LF Rodríguez Vallejo - repositorio.unal.edu.co
Colombia es un país multiétnico donde la población con mezcla europea (AE) predominó
después del descubrimiento de América en 1942. Sin embargo, una gran proporción de la …
después del descubrimiento de América en 1942. Sin embargo, una gran proporción de la …
A Novel Association between the 27-bp Deletion and 538G> A Mutation in the ABCC11 Gene
YS Hori, A Yamada, N Matsuda, Y Ono, D Starenki… - Human Biology, 2017 - muse.jhu.edu
A single nucleotide polymorphism in the ABCC11 gene, 538G> A (rs17822931), is known to
determine human ear wax type. The G/G and G/A genotypes correspond to the wet type …
determine human ear wax type. The G/G and G/A genotypes correspond to the wet type …
Relación de los genes HGSNAT, TTN Y ABCC8 con el fenotipo de la distrofia muscular congénita en una familia de Antioquia-Colombia.
YA García Rodríguez - 2021 - repository.ces.edu.co
NGS test: Novel ABCC8 K1411N Mutation Linked with Diabetes.
B Tokat, F Yanar, D Kanca-Demirci, N Gul… - …, 2022 - search.ebscohost.com
Objective: ATP-binding cassette transporter sub-family C member 8 (ABCC8) is involved in
the formation of the sulfonylurea receptor-1 protein, a subunit of ATP-sensitive potassium …
the formation of the sulfonylurea receptor-1 protein, a subunit of ATP-sensitive potassium …
Asociación del polimorfismo rs2231142 del gen ABCG2 con el ácido úrico sérico y con los componentes del síndrome metabólico en niños de 6 a 12 años de edad
LI Ibarra Rodríguez - 2020 - eprints.uanl.mx
El ácido úrico sérico (AUs) se ha identificado como un indicador de riesgo para el síndrome
metabólico (SM). Se ha encontrado asociación entre niveles elevados de AUs con el …
metabólico (SM). Se ha encontrado asociación entre niveles elevados de AUs con el …