Tusié-Luna, Teresa : rechercher sur Z-Library

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1

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

Lobato, M. Natividad, Ordóñez-Sánchez, M. Luisa, Tusié-Luna, M. Teresa, Meseguer, Anna

Journal:

Année:

1999

Langue:

english

Fichier:

PDF, 452 KB

english, 1999

2

Familial hypobetalipoproteinemia in a hospital survey: genetics, metabolism and non-alcoholic fatty liver disease

Gutiérrez-Cirlos, Carlos, Luisa Ordóñez-Sánchez, María, Teresa Tusié-Luna, María, Patterson, Bruce W., Schonfeld, Gustav, Aguilar-Salinas, Carlos A.

Journal:

Annals of Hepatology

Année:

2011

Fichier:

PDF, 244 KB

2011

3

Mutations in Steroid 21-Hydroxylase (CYP21)

Perrin C. White, Maria-Teresa Tusie-Luna, Maria I. New, Phyllis W. Speiser

Journal:

Année:

1994

Langue:

english

Fichier:

PDF, 576 KB

english, 1994

4

Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer’s disease in Mexican families

Petra Yescas, Adriana Huertas-Vazquez, María Teresa Villarreal-Molina, Astrid Rasmussen, María Teresa Tusié-Luna, Marisol López, Samuel Canizales-Quinteros, María Elisa Alonso

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 121 KB

english, 2006

5

GENEHUNTER versus SimWalk2 in the context of an extended kindred and a qualitative trait locus

Sandra Romero-Hidalgo, Eliane R. Rodrigues, Eduardo Gutiérrez-Peña, Laura Riba, María Teresa Tusié-Luna

Journal:

Année:

2005

Langue:

english

Fichier:

PDF, 312 KB

english, 2005

6

Estimating Ethnic Admixture from Pedigree Data

Janet S. Sinsheimer, Christopher L. Plaisier, Adriana Huertas-Vazquez, Carlos Aguilar-Salinas, Teresa Tusie-Luna, Päivi Pajukanta, Kenneth Lange

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 184 KB

english, 2008

7

Familial Hypercholesterolemia Due to Ligand-Defective Apolipoprotein B100.: First Case Report in a Mexican Family

Ludivina Robles-Osorio, Ma.Luisa Ordoñez, Carlos A Aguilar-Salinas, Moisés Aurón-Gómez, Ma.Teresa Tusié-Luna, Francisco J Gómez-Pérez, Juan A Rull-Rodrigo

Journal:

Archives of Medical Research

Année:

2003

Langue:

english

Fichier:

PDF, 210 KB

english, 2003

8

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

Laura del Bosque-Plata, Carlos A Aguilar-Salinas, Marı́a Teresa Tusié-Luna, Salvador Ramı́rez-Jiménez, Maribel Rodrı́guez-Torres, Moisés Aurón-Gómez, Erika Ramı́rez, Marı́a Luisa Velasco-Pérez, Alfred

Journal:

Molecular Genetics and Metabolism

Année:

2004

Langue:

english

Fichier:

PDF, 100 KB

english, 2004

9

The non-synonymous Arg230Cys variant (R230C) of the ATP-binding cassette transporter A1 is associated with low HDL cholesterol concentrations in Mexican adults: A population based nation wide study

Carlos A. Aguilar-Salinas, Samuel Canizales-Quinteros, Rosalba Rojas-Martínez, Roopa Mehta, Rosario Rodriguez-Guillén, María Luisa Ordoñez-Sanchez, Laura Riba, María Teresa Tusié-Luna

Journal:

Atherosclerosis

Année:

2011

Langue:

english

Fichier:

PDF, 140 KB

english, 2011

10

1.P.225 Description of a familial hypercholasterolemia kindred protected against atherosclerosis by a genetic form of hyperalphalipoproteinemia

Carlos A. Aguilar, Eduardo Reyes, Teresa Tusie-Luna, Laura Riba-Ramirez, Salvador Remirez-Jimenez, Jorge Gonzalez-Barranco, Francisco J. Gómez-Pérez, Juan A. Rull

Journal:

Atherosclerosis

Année:

1997

Langue:

english

Fichier:

PDF, 183 KB

english, 1997

11

With the finished human genome in hand, what next?

Julio Collado-Vides, Arturo Medrano-Soto, Maria Teresa Tusié-Luna

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 60 KB

english, 2003

12

Genetic and environmental determinants of the susceptibility of Amerindian derived populations for having hypertriglyceridemia

Aguilar-Salinas, Carlos A., Tusie-Luna, Teresa, Pajukanta, Päivi

Journal:

Année:

2014

Langue:

english

Fichier:

PDF, 401 KB

english, 2014

13

Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A

Medeiros-Domingo, Argelia, Tan, Bi-Hua, Iturralde-Torres, Pedro, Tester, David J., Tusié-Luna, Teresa, Makielski, Jonathan C., Ackerman, Michael J.

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 1.52 MB

english, 2009

14

A Mutation (Pro-30 to Leu) in CYP 21 Represents a Potential Nonclassic Steroid 21-Hydroxylase Deficiency Allele

Tusie-Luna, Maria-Teresa, Speiser, Phyllis W., Dumic, Miro, New, Maria I., White, Perrin C.

Journal:

Molecular Endocrinology

Année:

1991

Langue:

english

Fichier:

PDF, 899 KB

english, 1991

15

Primary amenorrhea in two sisters: description of a Mexican family with 17α hydroxylase-17 lyase deficiency caused by arginine – stop mutation

Escamilla-Márquez, Marco Antonio, Garduño-Garcia, José de Jesús, Ordóñez-Sanchez, Maria Luisa, Reza-Albarrán, Alfredo, Tusie-Luna, María Teresa, Gómez Pérez, Francisco Javier, Aguilar-Salinas, Carlos

Journal:

Gynecological Endocrinology

Année:

2012

Langue:

english

Fichier:

PDF, 630 KB

english, 2012

16

A Systems Genetics Approach Implicates USF1, FADS3, and Other Causal Candidate Genes for Familial Combined Hyperlipidemia

Plaisier, Christopher L., Horvath, Steve, Huertas-Vazquez, Adriana, Cruz-Bautista, Ivette, Herrera, Miguel F., Tusie-Luna, Teresa, Aguilar-Salinas, Carlos, Pajukanta, Päivi, Storey, John D.

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 590 KB

english, 2009

17

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

Rasmussen, Astrid, Nava-Salazar, Sonia, Yescas, Petra, Alonso, Elisa, Revuelta, Rogelio, Ortiz, Iván, Canizales-Quinteros, Samuel, Tusié-Luna, María Teresa, López-López, Marisol

Journal:

Journal of Neurosurgery

Année:

2006

Langue:

english

Fichier:

PDF, 265 KB

english, 2006

18

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

Maria-Teresa Tusie-Luna and Perrin C. White

Journal:

Proceedings of the National Academy of Sciences

Année:

1995

Langue:

english

Fichier:

PDF, 1.14 MB

english, 1995

19

Expression of 11β-Hydroxysteroid Dehydrogenase Using Recombinant Vaccinia Virus

Agarwal, Anil K., Tusie-Luna, Maria-Teresa, Monder, Carl, White, Perrin C.

Journal:

Molecular Endocrinology

Année:

1990

Langue:

english

Fichier:

PDF, 795 KB

english, 1990

20

Hypoalphalipoproteinemia in populations of Native American ancestry: an opportunity to assess the interaction of genes and the environment

Aguilar-Salinas, Carlos A, Canizales-Quinteros, Samuel, Rojas-Martínez, Rosalba, Mehta, Roopa, Villarreal-Molina, Ma Teresa, Arellano-Campos, Olimpia, Riba, Laura, Gómez-Pérez, Francisco J, Tusié-Luna

Journal:

Current Opinion in Lipidology

Année:

2009

Langue:

english

Fichier:

PDF, 116 KB

english, 2009

21

The panorama of familial hypercholesterolemia in Latin America: a systematic review

Mehta, Roopa, Zubiran, Rafael, Martagon, Alexandro, Vazquez-Cardenas, Alejandra, Segura-Kato, Yayoi, Tusie-Luna, Maria Teresa, Aguilar-Salinas, Carlos A

Journal:

The Journal of Lipid Research

Année:

2016

Langue:

english

Fichier:

PDF, 1.53 MB

english, 2016

22

Searching for the Causal Variants of the Association Between Hypertriglyceridemia and the Genome-Wide Association Studies–Derived Signals?

Aguilar-Salinas, Carlos A., Sevilla González, Magdalena del Rocío, Tusie-Luna, María Teresa

Journal:

Circulation Cardiovascular Genetics

Année:

2017

Langue:

english

Fichier:

PDF, 301 KB

english, 2017

23

Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients

Lanata, Cristina M., Nititham, Joanne, Taylor, Kimberly E., Chung, Sharon A., Torgerson, Dara G., Seldin, Michael F., Pons-Estel, Bernardo A., Tusié-Luna, Teresa, Tsao, Betty P., Morand, Eric F., Alar

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 2.19 MB

english, 2018

24

Familial Hyperkalemic Hypertension Genotype With a Negative Phenotype: A CUL3 Mosaicism

Ostrosky-Frid, Mauricio, Chávez-Canales, María, Romo, Miriam, Grunfeld, Beatriz, Simsolo, Rosa, Segura-Kato, Yayoi, Tusié-Luna, Teresa, Gamba, Gerardo

Journal:

American Journal of Hypertension

Année:

2019

Fichier:

PDF, 817 KB

2019

25

The SLC16A11 Risk Haplotype for Type 2 Diabetes (T2D) Is Associated to Differentiated Responses in Weight Loss, and Glucose Metabolism After Treatments to Prevent T2D

Sevilla, Magdalena, Gomez-Velasco, Donaji, Cruz-Bautista, Ivette, Lazaro-Carrera, Laura, Almeda-Valdes, Paloma, Tusie-Luna, Teresa, Manning, Alisa, Aguilar-Salinas, Carlos

Journal:

Current Developments in Nutrition

Année:

2020

Fichier:

PDF, 81 KB

2020