Search research articles
Contact Us
Filters
Showing results (1-10 of 26) with videos related to
Page
of 3
Sort By:
Fertility and Sterility
|
April 17, 2007
Mutations of SYCP3 are rare in infertile Spanish men with meiotic arrest
Juanjo Martínez, Sandra Bonache, Alejandro Carvajal, et al.
International Journal of Andrology
|
February 15, 2007
Single nucleotide polymorphisms in succinate dehydrogenase subunits and citrate synthase genes: association results for impaired spermatogenesis
Sandra Bonache, Juanjo Martínez, Marlin Fernández, et al.
Human Reproduction (Oxford, England)
|
March 27, 2012
Sperm gene expression profile is related to pregnancy rate after insemination and is predictive of low fecundity in normozoospermic men
Sandra Bonache, Ana Mata, María Dolores Ramos, et al.
Gynecologic Oncology
|
August 6, 2013
Mutation analysis of the BCCIP gene for breast cancer susceptibility in breast/ovarian cancer families
Sandra Bonache, Sara Gutierrez-Enriquez, Anna Tenés, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 30, 2005
Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations
Satu Kinnunen, Sandra Bonache, Teresa Casals, et al.
Journal of Andrology
|
January 16, 2010
Changes in the expression profile of the meiosis-involved mismatch repair genes in impaired human spermatogenesis
Ernest Terribas, Sandra Bonache, Marta García-Arévalo, et al.
Journal of Cancer Research and Clinical Oncology
|
February 2, 2013
Mutation analysis of the SHFM1 gene in breast/ovarian cancer families
Sandra Bonache, Miguel de la Hoya, Sara Gutierrez-Enriquez, et al.
Plos One
|
November 1, 2012
Epigenetic disruption of the PIWI pathway in human spermatogenic disorders
Holger Heyn, Humberto J Ferreira, Lluís Bassas, et al.
Breast Cancer Research and Treatment
|
August 4, 2014
RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families
Ana Blanco, Sara Gutiérrez-Enríquez, Marta Santamariña, et al.
Molecular Therapy. Nucleic Acids
|
November 24, 2022
Antisense oligonucleotides targeting exon 11 are able to partially rescue the NF2-related schwannomatosis phenotype <i>in vitro</i>
Núria Catasús, Inma Rosas, Sandra Bonache, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 26) with videos related to
Sort By:
Page
of 3
Fertility and Sterility
|
April 17, 2007
Mutations of SYCP3 are rare in infertile Spanish men with meiotic arrest
Juanjo Martínez, Sandra Bonache, Alejandro Carvajal, et al.
International Journal of Andrology
|
February 15, 2007
Single nucleotide polymorphisms in succinate dehydrogenase subunits and citrate synthase genes: association results for impaired spermatogenesis
Sandra Bonache, Juanjo Martínez, Marlin Fernández, et al.
Human Reproduction (Oxford, England)
|
March 27, 2012
Sperm gene expression profile is related to pregnancy rate after insemination and is predictive of low fecundity in normozoospermic men
Sandra Bonache, Ana Mata, María Dolores Ramos, et al.
Gynecologic Oncology
|
August 6, 2013
Mutation analysis of the BCCIP gene for breast cancer susceptibility in breast/ovarian cancer families
Sandra Bonache, Sara Gutierrez-Enriquez, Anna Tenés, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 30, 2005
Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations
Satu Kinnunen, Sandra Bonache, Teresa Casals, et al.
Journal of Andrology
|
January 16, 2010
Changes in the expression profile of the meiosis-involved mismatch repair genes in impaired human spermatogenesis
Ernest Terribas, Sandra Bonache, Marta García-Arévalo, et al.
Journal of Cancer Research and Clinical Oncology
|
February 2, 2013
Mutation analysis of the SHFM1 gene in breast/ovarian cancer families
Sandra Bonache, Miguel de la Hoya, Sara Gutierrez-Enriquez, et al.
Plos One
|
November 1, 2012
Epigenetic disruption of the PIWI pathway in human spermatogenic disorders
Holger Heyn, Humberto J Ferreira, Lluís Bassas, et al.
Breast Cancer Research and Treatment
|
August 4, 2014
RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families
Ana Blanco, Sara Gutiérrez-Enríquez, Marta Santamariña, et al.
Molecular Therapy. Nucleic Acids
|
November 24, 2022
Antisense oligonucleotides targeting exon 11 are able to partially rescue the NF2-related schwannomatosis phenotype <i>in vitro</i>
Núria Catasús, Inma Rosas, Sandra Bonache, et al.
Page
of 3