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Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes

Diabetologia, 2009-08, Vol.52 (8), p.1528-1536

2009

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The influence of high-density lipoprotein (HDL) and HDL subfractions on insulin secretion and cholesterol efflux in pancreatic derived β-cells

Journal of endocrinological investigation, 2021-09, Vol.44 (9), p.1897-1904

2021

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R230C but not − 565C/T variant of the ABCA1 gene is associated with type 2 diabetes in Mexicans through an effect on lowering HDL-cholesterol levels

Journal of endocrinological investigation, 2020-08, Vol.43 (8), p.1061-1071

2020

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High frequency of T130I mutation of HNF4A gene in Mexican patients with early-onset type 2 diabetes

Clinical genetics, 2008-02, Vol.73 (2), p.185-187

2008

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Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus

The Journal of biological chemistry, 1990-12, Vol.265 (34), p.20916-20922

1990

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Gene Conversions and Unequal Crossovers Between CYP21 (Steroid 21- Hydroxylase Gene) and CYP21P Involve Different Mechanisms

Proceedings of the National Academy of Sciences - PNAS, 1995-11, Vol.92 (23), p.10796-10800

1995

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HNF-1α G574S is a functional variant with decreased transactivation activity

Diabetic medicine, 2006-12, Vol.23 (12), p.1295-1300

2006

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Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The Journal of clinical investigation, 1992-08, Vol.90 (2), p.584-595

1992

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The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex

Molecular endocrinology (Baltimore, Md.), 1991-10, Vol.5 (10), p.1513-1522

1991

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Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease

Journal of medical genetics, 1998-12, Vol.35 (12), p.1014-1019

1998

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Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population : identification of possible new mutations and high prevalence of apparent germ-line mutations

Human genetics, 1998-02, Vol.102 (2), p.170-177

1998

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A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

Molecular endocrinology (Baltimore, Md.), 1991-05, Vol.5 (5), p.685-692

1991

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Contribution of Chromosome 1q21‐q23 to Familial Combined Hyperlipidemia in Mexican Families

Annals of human genetics, 2004-09, Vol.68 (5), p.419-427

2004

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The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans

Journal of endocrinological investigation, 2021-03, Vol.44 (3), p.557-565

2021

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Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population

Human genetics, 1996-09, Vol.98 (3), p.376-379

1996

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R339H and P453S : CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions

Molecular endocrinology (Baltimore, Md.), 1992-08, Vol.6 (8), p.1318-1322

1992

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Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population

Molecular genetics and metabolism, 2004-02, Vol.81 (2), p.122-126

2004

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Early-onset type 2 diabetes : Metabolic and genetic characterization in the Mexican population

The journal of clinical endocrinology and metabolism, 2001, Vol.86 (1), p.220-226

2001

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Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease

Human heredity, 1999-01, Vol.49 (3), p.169-175

1999

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Mutations in Steroid 21-Hydroxylase (CYP21)

Human mutation, 1994, Vol.3 (4), p.373-378

1994

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Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma

Journal of neurosurgery, 2006-03, Vol.104 (3), p.389-394

2006

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Expression of 11 beta-hydroxysteroid dehydrogenase using recombinant vaccinia virus

Molecular endocrinology (Baltimore, Md.), 1990-12, Vol.4 (12), p.1827-1832

1990

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Strong Association of Socioeconomic Status and Genetic Ancestry in Latinos: Implications for Admixture Studies of Type 2 Diabetes

Racial Identities, Genetic Ancestry, and Health in South America, p.137-153

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Genetic Heterogeneity of Autosomal Dominant Hypercholesterolemia in Mexico

Archives of medical research, 2006, Vol.37 (1), p.102-108

2006

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Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes

The influence of high-density lipoprotein (HDL) and HDL subfractions on insulin secretion and cholesterol efflux in pancreatic derived β-cells

R230C but not − 565C/T variant of the ABCA1 gene is associated with type 2 diabetes in Mexicans through an effect on lowering HDL-cholesterol levels

High frequency of T130I mutation of HNF4A gene in Mexican patients with early-onset type 2 diabetes

Determination of functional effects of mutations in the steroid 21-hydroxylase gene (CYP21) using recombinant vaccinia virus

Gene Conversions and Unequal Crossovers Between CYP21 (Steroid 21- Hydroxylase Gene) and CYP21P Involve Different Mechanisms

HNF-1α G574S is a functional variant with decreased transactivation activity

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

The product of the CYP11B2 gene is required for aldosterone biosynthesis in the human adrenal cortex

Association of PPARG2 Pro12Ala Variant with Larger Body Mass Index in Mestizo and Amerindian Populations of Mexico

Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: evidence of different genetic mechanisms involved in the production of the disease

Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population : identification of possible new mutations and high prevalence of apparent germ-line mutations

A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

Contribution of Chromosome 1q21‐q23 to Familial Combined Hyperlipidemia in Mexican Families

The -514C>T polymorphism in the LIPC gene modifies type 2 diabetes risk through modulation of HDL-cholesterol levels in Mexicans

Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population

R339H and P453S : CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions

Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population

Early-onset type 2 diabetes : Metabolic and genetic characterization in the Mexican population

Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease

Mutations in Steroid 21-Hydroxylase (CYP21)

Von Hippel-Lindau disease germline mutations in Mexican patients with cerebellar hemangioblastoma

Expression of 11 beta-hydroxysteroid dehydrogenase using recombinant vaccinia virus

Strong Association of Socioeconomic Status and Genetic Ancestry in Latinos: Implications for Admixture Studies of Type 2 Diabetes

Genetic Heterogeneity of Autosomal Dominant Hypercholesterolemia in Mexico

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