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Lluís Bassas

Research Profile

Chemicals & Drugs

Disorders

Anatomy

Physiology

Concepts & Ideas

Meiosis

Genes & Molecular Sequences

Single Nucleotide Polymorphism

Procedures

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Publications

TOP 3
Sandra Bonache; Ana Mata; Maria Dolors Ramos; Lluís Bassas; Sara Larriba
Sperm gene expression profile is related to pregnancy rate after insemination and is predictive of low fecundity in normozoospermic men.
Holger Heyn; Juan Sandoval; Sergi Sayols; Lluís Bassas; Sandra Bonache; Manel Esteller; Humberto J Ferreira; Sara Larriba
Epigenetic disruption of the PIWI pathway in human spermatogenic disorders.
Ernest Terribas; Sandra Bonache; Marta García-Arévalo; Josvany Sánchez; Eladio Franco; Lluís Bassas; Sara Larriba
Changes in the expression profile of the meiosis-involved mismatch repair genes in impaired human spermatogenesis.

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All Publications

2012: Sandra Bonache; Ana Mata; Maria Dolors Ramos; Lluís Bassas; Sara Larriba
Sperm gene expression profile is related to pregnancy rate after insemination and is predictive of low fecundity in normozoospermic men.
Human reproduction (Oxford, England) 2012;27(6):1556-67.
2012: Holger Heyn; Juan Sandoval; Sergi Sayols; Lluís Bassas; Sandra Bonache; Manel Esteller; Humberto J Ferreira; Sara Larriba
Epigenetic disruption of the PIWI pathway in human spermatogenic disorders.
PloS one 2012;7(10):e47892.
2010: Ernest Terribas; Sandra Bonache; Marta García-Arévalo; Josvany Sánchez; Eladio Franco; Lluís Bassas; Sara Larriba
Changes in the expression profile of the meiosis-involved mismatch repair genes in impaired human spermatogenesis.
Journal of andrology 2010;31(4):346-57.
2009: Laia Masvidal; Javier Giménez; María D Ramos; Christian Domingo; Antoni Farré; Lluís Bassas; Teresa Casals
The p.Arg258Gly mutation in intracellular loop 2 of CFTR is associated with CFTR-related disorders.
Genetic testing and molecular biomarkers 2009;13(6):765-8.
2007: Juanjo Martínez; Sandra Bonache; Alejandro Carvajal; Lluís Bassas; Sara Larriba
Mutations of SYCP3 are rare in infertile Spanish men with meiotic arrest.
Fertility and sterility 2007;88(4):988-9.
2007: Sandra Bonache; Juanjo Martínez; Marlin Fernández; Lluís Bassas; Sara Larriba
Single nucleotide polymorphisms in succinate dehydrogenase subunits and citrate synthase genes: association results for impaired spermatogenesis.
International journal of andrology 2007;30(3):144-52.
2005: Sara Larriba; Sandra Bonache; J Sarquella; Maria Dolors Ramos; Javier Giménez; Lluís Bassas; Teresa Casals
Molecular evaluation of CFTR sequence variants in male infertility of testicular origin.
International journal of andrology 2005;28(5):284-90.
2004: Joshua D Groman; Timothy W Hefferon; Teresa Casals; Lluís Bassas; Xavier Estivill; Marie Des Georges; Caroline Guittard; Monika Koudova; MARGARET D FALLIN; Krisztina Nemeth; Gyorgy Fekete; Ludovit Kadasi; Kenneth Friedman; Martin Schwarz; Cristina Bombieri; Pier Franco Pignatti; Emmanuel Kanavakis; Maria Tzetis; Marianne Schwartz; Giuseppe Novelli; Maria Rosaria D'Apice; Agnieszka Sobczynska-Tomaszewska; Jerzy Bal; Manfred Stuhrmann; Milan Macek Jr.; Mireille Claustres; Garry R Cutting
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign.
American journal of human genetics 2004;74(1):176-9.
2001: Sara Larriba; Lluís Bassas; S Egozcue; Javier Giménez; Maria Dolors Ramos; O Briceño; Xavier Estivill; Teresa Casals
Adenosine triphosphate-binding cassette superfamily transporter gene expression in severe male infertility.
Biology of reproduction 2001;65(2):394-400.
2000: Teresa Casals; Lluís Bassas; S Egozcue; Maria Dolors Ramos; Javier Giménez; A Segura; F Garcia; M Carrera; Sara Larriba; J Sarquella; Xavier Estivill
Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens.
Human reproduction (Oxford, England) 2000;15(7):1476-83.
1998: Sara Larriba; Lluís Bassas; J Gimenez; Maria Dolors Ramos; A Segura; Virginia Nunes; Xavier Estivill; Teresa Casals
Testicular CFTR splice variants in patients with congenital absence of the vas deferens.
Human molecular genetics 1998;7(11):1739-43.