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The Annals of Thoracic Surgery
|
February 16, 2002
Aortic wall alterations after use of gelatin-resorcinol-formalin glue
Matthias Kirsch, Maryvonne Ginat, Laure Lecerf, et al.
Biosensors & Bioelectronics
|
April 20, 2006
DNA immobilisation procedures for surface plasmon resonance imaging (SPRI) based microarray systems
Ilaria Mannelli, Laure Lecerf, Mohamed Guerrouache, et al.
European Journal of Medical Genetics
|
September 29, 2012
Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions
Narjes Guediche, Lucie Tosca, Marc Nouchy, et al.
Haematologica
|
July 18, 2012
Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region
Elyes Slim Ghedira, Laure Lecerf, Emmanuelle Faubert, et al.
European Journal of Human Genetics : EJHG
|
March 2, 2012
Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4
Nadége Bondurand, Virginie Fouquet, Viviane Baral, et al.
Gastroenterology
|
January 9, 2017
Differentiation of Mouse Enteric Nervous System Progenitor Cells Is Controlled by Endothelin 3 and Requires Regulation of Ednrb by SOX10 and ZEB2
Yuli Watanabe, Laure Stanchina, Laure Lecerf, et al.
Human Molecular Genetics
|
June 11, 2015
Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutations
Asma Chaoui, Anthula Kavo, Viviane Baral, et al.
Human Mutation
|
December 21, 2013
An impairment of long distance SOX10 regulatory elements underlies isolated Hirschsprung disease
Laure Lecerf, Anthula Kavo, Macarena Ruiz-Ferrer, et al.
The American Journal of Pathology
|
March 26, 2003
Human urinary bladder transitional cell carcinomas acquire the functional Fas ligand during tumor progression
Dominique Chopin, Reza Barei-Moniri, Pascale Maillé, et al.
Human Mutation
|
February 26, 2017
EDNRB mutations cause Waardenburg syndrome type II in the heterozygous state
Sarah Issa, Nadege Bondurand, Emmanuelle Faubert, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
The Annals of Thoracic Surgery
|
February 16, 2002
Aortic wall alterations after use of gelatin-resorcinol-formalin glue
Matthias Kirsch, Maryvonne Ginat, Laure Lecerf, et al.
Biosensors & Bioelectronics
|
April 20, 2006
DNA immobilisation procedures for surface plasmon resonance imaging (SPRI) based microarray systems
Ilaria Mannelli, Laure Lecerf, Mohamed Guerrouache, et al.
European Journal of Medical Genetics
|
September 29, 2012
Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions
Narjes Guediche, Lucie Tosca, Marc Nouchy, et al.
Haematologica
|
July 18, 2012
Estimation of the difference in HbF expression due to loss of the 5' δ-globin BCL11A binding region
Elyes Slim Ghedira, Laure Lecerf, Emmanuelle Faubert, et al.
European Journal of Human Genetics : EJHG
|
March 2, 2012
Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4
Nadége Bondurand, Virginie Fouquet, Viviane Baral, et al.
Gastroenterology
|
January 9, 2017
Differentiation of Mouse Enteric Nervous System Progenitor Cells Is Controlled by Endothelin 3 and Requires Regulation of Ednrb by SOX10 and ZEB2
Yuli Watanabe, Laure Stanchina, Laure Lecerf, et al.
Human Molecular Genetics
|
June 11, 2015
Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutations
Asma Chaoui, Anthula Kavo, Viviane Baral, et al.
Human Mutation
|
December 21, 2013
An impairment of long distance SOX10 regulatory elements underlies isolated Hirschsprung disease
Laure Lecerf, Anthula Kavo, Macarena Ruiz-Ferrer, et al.
The American Journal of Pathology
|
March 26, 2003
Human urinary bladder transitional cell carcinomas acquire the functional Fas ligand during tumor progression
Dominique Chopin, Reza Barei-Moniri, Pascale Maillé, et al.
Human Mutation
|
February 26, 2017
EDNRB mutations cause Waardenburg syndrome type II in the heterozygous state
Sarah Issa, Nadege Bondurand, Emmanuelle Faubert, et al.
Page
of 2