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Florence Coulet

Showing results (31-40 of 114) with videos related to

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Basic and Clinical Andrology|March 18, 2015
In Vitro fertilization failure of normozoospermic men: search for a lack of testicular isozyme of angiotensin-converting enzymeSelima Fourati Ben Mustapha, Florence Coulet, Mélanie Eyries, et al.
Proteomics. Clinical Applications|December 8, 2010
Proteomic analysis of BRCA1-depleted cell line reveals a putative role for replication protein A2 up-regulation in BRCA1 breast tumor developmentJulien Bouley, Cédric Pionneau, Justine Varinot, et al.
Familial Cancer|July 20, 2010
MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversionsJérémie H Lefevre, Chrystelle Colas, Florence Coulet, et al.
European Journal of Human Genetics : EJHG|March 12, 2022
Detection of a pathogenic Alu element insertion in PALB2 gene from targeted NGS diagnostic dataMélanie Eyries, Olivier Ariste, Gaelle Legrand, et al.
Lancet (London, England)|October 7, 2004
Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathiesHanna Debiec, Jeroen Nauta, Florence Coulet, et al.
Human Mutation|March 7, 2014
The UMD-APC database, a model of nation-wide knowledge base: update with data from 3,581 variationsPhilippe Grandval, Martine Blayau, Marie-Pierre Buisine, et al.
The Prostate|June 2, 2022
DNA damage repair gene germline profiling for metastatic prostate cancer patients of different ancestriesBilal Abdi, Noemie Basset, Emmanuel Perrot, et al.
European Thyroid Journal|December 5, 2024
Performance of the AmpliSeq NGS panel in thyroid nodules with indeterminate cytologyWiame Potonnier, Erell Guillerm, Claude Bigorgne, et al.
Journal of Medical Genetics|September 16, 2022
Comprehensive RNA and protein functional assessments contribute to the clinical interpretation of <i>MSH2</i> variants causing in-frame splicing alterationsLaëtitia Meulemans, Stéphanie Baert Desurmont, Marie-Christine Waill, et al.
Oncology Reports|April 22, 2008
First genetic analysis in Tunisian familial adenomatous polyposis probandsKarim Bougatef, Raja Marrakchi, Amel Moussa, et al.
Pageof 12

Showing results (31-40 of 114) with videos related to

Sort By:
Pageof 12
Basic and Clinical Andrology|March 18, 2015
In Vitro fertilization failure of normozoospermic men: search for a lack of testicular isozyme of angiotensin-converting enzymeSelima Fourati Ben Mustapha, Florence Coulet, Mélanie Eyries, et al.
Proteomics. Clinical Applications|December 8, 2010
Proteomic analysis of BRCA1-depleted cell line reveals a putative role for replication protein A2 up-regulation in BRCA1 breast tumor developmentJulien Bouley, Cédric Pionneau, Justine Varinot, et al.
Familial Cancer|July 20, 2010
MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversionsJérémie H Lefevre, Chrystelle Colas, Florence Coulet, et al.
European Journal of Human Genetics : EJHG|March 12, 2022
Detection of a pathogenic Alu element insertion in PALB2 gene from targeted NGS diagnostic dataMélanie Eyries, Olivier Ariste, Gaelle Legrand, et al.
Lancet (London, England)|October 7, 2004
Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathiesHanna Debiec, Jeroen Nauta, Florence Coulet, et al.
Human Mutation|March 7, 2014
The UMD-APC database, a model of nation-wide knowledge base: update with data from 3,581 variationsPhilippe Grandval, Martine Blayau, Marie-Pierre Buisine, et al.
The Prostate|June 2, 2022
DNA damage repair gene germline profiling for metastatic prostate cancer patients of different ancestriesBilal Abdi, Noemie Basset, Emmanuel Perrot, et al.
European Thyroid Journal|December 5, 2024
Performance of the AmpliSeq NGS panel in thyroid nodules with indeterminate cytologyWiame Potonnier, Erell Guillerm, Claude Bigorgne, et al.
Journal of Medical Genetics|September 16, 2022
Comprehensive RNA and protein functional assessments contribute to the clinical interpretation of <i>MSH2</i> variants causing in-frame splicing alterationsLaëtitia Meulemans, Stéphanie Baert Desurmont, Marie-Christine Waill, et al.
Oncology Reports|April 22, 2008
First genetic analysis in Tunisian familial adenomatous polyposis probandsKarim Bougatef, Raja Marrakchi, Amel Moussa, et al.
Pageof 12