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Scavenger receptor-B1 and luteal function in mice

MIRANDA JIMÉNEZ, Leonor; BINELLI, Mario; BERTOLIN, Kalyne; PELLETIER, R. M; MURPHY, Bruce Daniel (New York, 2010)

During luteinization, circulating high-density lipoproteins supply cholesterol to ovarian cells via the scavenger receptor-B1 (SCARB1). In the mouse, SCARB1 is expressed in cytoplasm and periphery of theca, granulosa, and ...

Influence of SCARB1 polymorphisms on serum lipids of hypercholesterolemic individuals treated with atorvastatin

CERDA, Alvaro; GENVIGIR, Fabiana D. V.; ARAZI, Simone S.; HIRATA, Mario H.; Dorea, Egidio Lima; BERNIK, Marcia M. S.; BERTOLAMI, Marcelo C.; FALUDI, Andre A.; HIRATA, Rosario D. C. (ELSEVIER SCIENCE BV, 2010)

Background: The SR-BI is a key component on the cholesterol metabolism. Polymorphisms in the SR-BI gene (SCARB1) were related with variations on plasma lipoprotein profile and other risk factors for cardiovascular disease. ...

Estudo molecular dos genes ABCA1, ABCG1, ABCG5, ABCG8 e SCARB1 em amostra populacional brasileira assintomáticaMolecular study of ABCA1, ABCG1, ABCG5, ABCG8 and SCARB1 genes in an asymptomatic brazilian population sample

Zago, Vanessa Helena de Souza, 1984- ([s.n.], 2015)

The association study of lipid metabolism gene polymorphisms with AMD identifies a protective role for APOE-E2 allele in the wet form in a Northern Spanish population

Fernández-Vega B.; García M.; Olivares L.; Álvarez L.; González-Fernández A.; Artime E.; Fernández-Vega Cueto A.; Cobo T.; Coca-Prados M.; Vega J.A.; González-Iglesias H. (Blackwell Publishing Ltd, 2020)

Estudo de frequência de polimorfismos em genes envolvidos no risco de efeitos adversos da risperidona em uma amostra da população brasileiraFrequency of polymorphisms in genes involved in the risk of adverse effects of risperidone in a sample in the Brazilian population

Henriques, Taciane Barbosa, 1989- ([s.n.], 2016)

Farmacogenética dos efeitos adversos da risperidona em crianças e adolescentesPharmacogenetics of risperidone induced side effects in children and adolescents

Santos Júnior, Amilton dos, 1983- ([s.n.], 2015)

Unusual genetic variants associated with hypercholesterolemia in Argentina

Corral, Pablo; Geller, Andrew S.; Polisecki, Eliana Y.; Lopez, Graciela Ines; Bañares, Virginia Gabriela; Cacciagiu, Leonardo; Berg, Gabriela Alicia; Hegele, Robert A.; Schaefer, Ernst J.; Schreier, Laura Ester (Elsevier Ireland, 2018-10)

Background and aims: Marked hypercholesterolemia, defined as low density lipoprotein cholesterol (LDL-C) levels ≥ 190 mg/dL, may be due to LDLR, APOB, and PCSK9 variants. In a recent analysis, only 1.7% of cases had such ...

Hyperprolactinemia In Children And Adolescents With Use Of Risperidone: Clinical And Molecular Genetics Aspects.

Dos Santos Júnior, Amilton; Henriques, Taciane Barbosa; de Mello, Maricilda Palandi; Neto, Adriana Perez Ferreira; Paes, Lúcia Arisaka; Torre, Osmar Henrique Della; Sewaybricker, Letícia Esposito; Fontana, Thiago Salum; Celeri, Eloisa Helena Rubello Valler; Júnior, Gil Guerra; Dalgalarrondo, Paulo (2015)

Hyperprolactinemia In Children And Adolescents With Use Of Risperidone: Clinical And Molecular Genetics Aspects

dos Santos Junior; Amilton; Henriques; Taciane Barbosa; de Mello; Maricilda Palandi; Ferreira Neto; Adriana Perez; Paes; Lucia Arisaka; Della Torre; Osmar Henrique; Sewaybricker; Leticia Esposito; Fontana; Thiago Salum; Rubello Valler Celeri; Eloisa Helena; Guerra Junior; Gil; Dalgalarrondo; Paulo (MARY ANN LIEBERT, INCNEW ROCHELLE, 2015)

Identificación de variantes genómicas del gen GBA en pacientes con patologías diferentes y no diagnosticados clínicamente con enfermedad de Gaucher en el suroccidente colombiano.

Arturo Terranova, Daniela (Universidad del ValleColombiaFACULTAD DE SALUDMAESTRÍA EN CIENCIAS BIOMÉDICAS, 2021)

La Enfermedad de Gaucher (EG) es un trastorno genético autosómico recesivo, causado por la deficiencia de la enzima lisosomal B-Glucocerebrosidasa ácida (GBA). En Colombia se ha estimado una prevalencia de 1:266.441 ...