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Marine Guillaud-Bataille

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European Journal of Neurology|December 20, 2024
Hereditary spastic paraplegias: When to expect bladder dysfunction a genetic and urodynamic studyPauline Lallemant-Dudek, Marine Guillaud-Bataille, Claire Hentzen, et al.
Nucleic Acids Research|October 10, 2006
Expression of C-terminal deleted p53 isoforms in neuroblastomaDavid Goldschneider, Emilie Horvilleur, Louis-François Plassa, et al.
Bioinformatics (Oxford, England)|October 17, 2019
SpliceLauncher: a tool for detection, annotation and relative quantification of alternative junctions from RNAseq dataRaphaël Leman, Valentin Harter, Alexandre Atkinson, et al.
Nucleic Acids Research|July 31, 2004
Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGHMarine Guillaud-Bataille, Alexander Valent, Pascal Soularue, et al.
International Journal of Molecular Sciences|July 29, 2023
Combined Tumor-Based <i>BRCA1/2</i> and <i>TP53</i> Mutation Testing in Ovarian CancerEdith Borcoman, Elizabeth Santana Dos Santos, Catherine Genestie, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2011
Clinical and pathophysiological implications of chromosomal alterations in adrenocortical tumors: an integrated genomic approachOlivia Barreau, Aurélien de Reynies, Hortense Wilmot-Roussel, et al.
Cancer Genetics and Cytogenetics|August 25, 2004
Alternative pathways of MYCN gene copy number increase in primary neuroblastoma tumorsAlexander Valent, Marine Guillaud-Bataille, Chantal Farra, et al.
The Journal of Clinical Endocrinology and Metabolism|March 16, 2012
TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paragangliomaNassera Abermil, Marine Guillaud-Bataille, Nelly Burnichon, et al.
European Journal of Human Genetics : EJHG|May 7, 2021
Evidence of mosaicism in SPAST variant carriers in four French familiesChloé Angelini, Cyril Goizet, Samia Ait Said, et al.
Human Mutation|April 2, 2010
Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an updateAnélia Horvath, Jérôme Bertherat, Lionel Groussin, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
European Journal of Neurology|December 20, 2024
Hereditary spastic paraplegias: When to expect bladder dysfunction a genetic and urodynamic studyPauline Lallemant-Dudek, Marine Guillaud-Bataille, Claire Hentzen, et al.
Nucleic Acids Research|October 10, 2006
Expression of C-terminal deleted p53 isoforms in neuroblastomaDavid Goldschneider, Emilie Horvilleur, Louis-François Plassa, et al.
Bioinformatics (Oxford, England)|October 17, 2019
SpliceLauncher: a tool for detection, annotation and relative quantification of alternative junctions from RNAseq dataRaphaël Leman, Valentin Harter, Alexandre Atkinson, et al.
Nucleic Acids Research|July 31, 2004
Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGHMarine Guillaud-Bataille, Alexander Valent, Pascal Soularue, et al.
International Journal of Molecular Sciences|July 29, 2023
Combined Tumor-Based <i>BRCA1/2</i> and <i>TP53</i> Mutation Testing in Ovarian CancerEdith Borcoman, Elizabeth Santana Dos Santos, Catherine Genestie, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2011
Clinical and pathophysiological implications of chromosomal alterations in adrenocortical tumors: an integrated genomic approachOlivia Barreau, Aurélien de Reynies, Hortense Wilmot-Roussel, et al.
Cancer Genetics and Cytogenetics|August 25, 2004
Alternative pathways of MYCN gene copy number increase in primary neuroblastoma tumorsAlexander Valent, Marine Guillaud-Bataille, Chantal Farra, et al.
The Journal of Clinical Endocrinology and Metabolism|March 16, 2012
TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paragangliomaNassera Abermil, Marine Guillaud-Bataille, Nelly Burnichon, et al.
European Journal of Human Genetics : EJHG|May 7, 2021
Evidence of mosaicism in SPAST variant carriers in four French familiesChloé Angelini, Cyril Goizet, Samia Ait Said, et al.
Human Mutation|April 2, 2010
Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an updateAnélia Horvath, Jérôme Bertherat, Lionel Groussin, et al.
Pageof 5