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

Eric Pasmant

Showing results (21-30 of 124) with videos related to

Pageof 13
Sort By:
Medecine Sciences : M/S|July 13, 2010
[The amazing story of ANRIL, a long non-coding RNA]Eric Pasmant, Ingrid Laurendeau, Audrey Sabbagh, et al.
Blood|August 1, 2009
SPRED1 disorder and predisposition to leukemia in childrenEric Pasmant, Paola Ballerini, Helene Lapillonne, et al.
Journal of Visualized Experiments : Jove|October 27, 2025
An Orthotopic Sciatic Nerve Xenograft for Neurofibromatosis Type 1 NeurofibromasManuela Ye, Aurélien Bore, Sophie Richon, et al.
Human Mutation|July 4, 2012
Review and update of SPRED1 mutations causing Legius syndromeHilde Brems, Eric Pasmant, Rick Van Minkelen, et al.
Genes & Development|July 11, 2015
Chaperoning 5S RNA assemblyClément Madru, Simon Lebaron, Magali Blaud, et al.
BMC Medical Genomics|March 6, 2024
Correlation between large rearrangements and patient phenotypes in NF1 deletion syndrome: an update and reviewLaurence Pacot, Milind Girish, Samantha Knight, et al.
The Journal of Investigative Dermatology|May 1, 2026
Phenotype of neurofibromatosis 1: a comparison study between NF1 mutant mice and humansLaura Fertitta, Fanny Coulpier, Layna Oubrou, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1Laurence Pacot, Albain Chansavang, Sébastien Jacques, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Characterization of a 7.6-Mb germline deletion encompassing the NF1 locus and about a hundred genes in an NF1 contiguous gene syndrome patientEric Pasmant, Aurélie de Saint-Trivier, Ingrid Laurendeau, et al.
Medicine|December 20, 2019
McCune Albright syndrome is a genetic predisposition to intraductal papillary and mucinous neoplasms of the pancreas associated pancreatic cancer in relation with GNAS somatic mutation - a case reportSébastien Gaujoux, Eric Pasmant, Caroline Silve, et al.
Pageof 13

Showing results (21-30 of 124) with videos related to

Sort By:
Pageof 13
Medecine Sciences : M/S|July 13, 2010
[The amazing story of ANRIL, a long non-coding RNA]Eric Pasmant, Ingrid Laurendeau, Audrey Sabbagh, et al.
Blood|August 1, 2009
SPRED1 disorder and predisposition to leukemia in childrenEric Pasmant, Paola Ballerini, Helene Lapillonne, et al.
Journal of Visualized Experiments : Jove|October 27, 2025
An Orthotopic Sciatic Nerve Xenograft for Neurofibromatosis Type 1 NeurofibromasManuela Ye, Aurélien Bore, Sophie Richon, et al.
Human Mutation|July 4, 2012
Review and update of SPRED1 mutations causing Legius syndromeHilde Brems, Eric Pasmant, Rick Van Minkelen, et al.
Genes & Development|July 11, 2015
Chaperoning 5S RNA assemblyClément Madru, Simon Lebaron, Magali Blaud, et al.
BMC Medical Genomics|March 6, 2024
Correlation between large rearrangements and patient phenotypes in NF1 deletion syndrome: an update and reviewLaurence Pacot, Milind Girish, Samantha Knight, et al.
The Journal of Investigative Dermatology|May 1, 2026
Phenotype of neurofibromatosis 1: a comparison study between NF1 mutant mice and humansLaura Fertitta, Fanny Coulpier, Layna Oubrou, et al.
European Journal of Human Genetics : EJHG|February 2, 2023
Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1Laurence Pacot, Albain Chansavang, Sébastien Jacques, et al.
European Journal of Human Genetics : EJHG|July 24, 2008
Characterization of a 7.6-Mb germline deletion encompassing the NF1 locus and about a hundred genes in an NF1 contiguous gene syndrome patientEric Pasmant, Aurélie de Saint-Trivier, Ingrid Laurendeau, et al.
Medicine|December 20, 2019
McCune Albright syndrome is a genetic predisposition to intraductal papillary and mucinous neoplasms of the pancreas associated pancreatic cancer in relation with GNAS somatic mutation - a case reportSébastien Gaujoux, Eric Pasmant, Caroline Silve, et al.
Pageof 13