Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T Bienvenu

Showing results (51-60 of 92) with videos related to

Pageof 10
Sort By:
Hepatology (Baltimore, Md.)|December 1, 1994
FK 506 renal toxicity and lack of detectable cytochrome P-450 3A in the liver graft of a patient undergoing liver transplantationA Lemoine, D Azoulay, A Dennison, et al.
Neurology|April 25, 2008
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndromeJ Nectoux, N Bahi-Buisson, I Guellec, et al.
Vascular Pharmacology|September 27, 2005
Reduced exhaled NO is related to impaired nasal potential difference in patients with cystic fibrosisJ Texereau, I Fajac, D Hubert, et al.
Annales De Genetique|May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardationP Billuart, J Chelly, A Carrié, et al.
Human Mutation|August 29, 2001
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategyT Bienvenu, I Souville, K Poirier, et al.
Human Reproduction (Oxford, England)|January 15, 2005
Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French studyI E Aknin-Seifer, R L Touraine, H Lejeune, et al.
American Journal of Human Genetics|April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.
Clinical Genetics|April 30, 2017
The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C functionC T Gordon, A Tessier, Z Demir, et al.
American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2020
Penetrance is a critical parameter for assessing the disease liability of CFTR variantsA Boussaroque, M-P Audrézet, C Raynal, et al.
Pageof 10

Showing results (51-60 of 92) with videos related to

Sort By:
Pageof 10
Hepatology (Baltimore, Md.)|December 1, 1994
FK 506 renal toxicity and lack of detectable cytochrome P-450 3A in the liver graft of a patient undergoing liver transplantationA Lemoine, D Azoulay, A Dennison, et al.
Neurology|April 25, 2008
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndromeJ Nectoux, N Bahi-Buisson, I Guellec, et al.
Vascular Pharmacology|September 27, 2005
Reduced exhaled NO is related to impaired nasal potential difference in patients with cystic fibrosisJ Texereau, I Fajac, D Hubert, et al.
Annales De Genetique|May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardationP Billuart, J Chelly, A Carrié, et al.
Human Mutation|August 29, 2001
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategyT Bienvenu, I Souville, K Poirier, et al.
Human Reproduction (Oxford, England)|January 15, 2005
Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French studyI E Aknin-Seifer, R L Touraine, H Lejeune, et al.
American Journal of Human Genetics|April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.
Clinical Genetics|April 30, 2017
The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C functionC T Gordon, A Tessier, Z Demir, et al.
American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2020
Penetrance is a critical parameter for assessing the disease liability of CFTR variantsA Boussaroque, M-P Audrézet, C Raynal, et al.
Pageof 10