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

N Nouri

Showing results (21-30 of 38) with videos related to

Pageof 4
Sort By:
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1995
The deafness locus (dn) maps to mouse chromosome 19B J Keats, N Nouri, J M Huang, et al.
Human Molecular Genetics|February 1, 1996
Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations: a variant nucleotide is associated with the number of CAG repeatsP Limprasert, N Nouri, R A Heyman, et al.
Alimentary Pharmacology & Therapeutics|August 11, 2005
Lower oesophageal sphincter pressure and timed barium oesophagogram: two objective parameters in the non-invasive assessment of primary achalasiaG Montazeri, N Nouri, A Estakhri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 15, 2025
Mortality in Tuberous sclerosis Complex: Current understandingsRowan Pentz, Lauren Sham, Maria Zak, et al.
Bratislavske Lekarske Listy|February 7, 2018
Decline in peripheral blood NKG2D+CD3+CD56+ NKT cells in metastatic colorectal cancer patientsM Gharagozloo, A Rezaei, H Kalantari, et al.
Brain, Behavior, and Immunity|May 14, 2013
Imatinib methanesulfonate reduces hippocampal amyloid-β and restores cognitive function following repeated endotoxin exposureMarielle K Weintraub, Courtney M Bisson, Jessica N Nouri, et al.
Genomics|November 1, 1991
Evidence for genetic heterogeneity in malignant hyperthermia susceptibilityR C Levitt, N Nouri, A E Jedlicka, et al.
The British Journal of Dermatology|December 27, 2017
An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstructionA Humbatova, R Maroofian, M-T Romano, et al.
Trials|November 12, 2020
A live-online mindfulness-based intervention for children living with epilepsy and their families: protocol for a randomized controlled trial of Making Mindfulness Matter©Klajdi Puka, Karen Bax, Andrea Andrade, et al.
Nature Genetics|June 1, 1994
A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10R A Preston, J C Post, B J Keats, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1995
The deafness locus (dn) maps to mouse chromosome 19B J Keats, N Nouri, J M Huang, et al.
Human Molecular Genetics|February 1, 1996
Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations: a variant nucleotide is associated with the number of CAG repeatsP Limprasert, N Nouri, R A Heyman, et al.
Alimentary Pharmacology & Therapeutics|August 11, 2005
Lower oesophageal sphincter pressure and timed barium oesophagogram: two objective parameters in the non-invasive assessment of primary achalasiaG Montazeri, N Nouri, A Estakhri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 15, 2025
Mortality in Tuberous sclerosis Complex: Current understandingsRowan Pentz, Lauren Sham, Maria Zak, et al.
Bratislavske Lekarske Listy|February 7, 2018
Decline in peripheral blood NKG2D+CD3+CD56+ NKT cells in metastatic colorectal cancer patientsM Gharagozloo, A Rezaei, H Kalantari, et al.
Brain, Behavior, and Immunity|May 14, 2013
Imatinib methanesulfonate reduces hippocampal amyloid-β and restores cognitive function following repeated endotoxin exposureMarielle K Weintraub, Courtney M Bisson, Jessica N Nouri, et al.
Genomics|November 1, 1991
Evidence for genetic heterogeneity in malignant hyperthermia susceptibilityR C Levitt, N Nouri, A E Jedlicka, et al.
The British Journal of Dermatology|December 27, 2017
An insertion mutation in HOXC13 underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstructionA Humbatova, R Maroofian, M-T Romano, et al.
Trials|November 12, 2020
A live-online mindfulness-based intervention for children living with epilepsy and their families: protocol for a randomized controlled trial of Making Mindfulness Matter©Klajdi Puka, Karen Bax, Andrea Andrade, et al.
Nature Genetics|June 1, 1994
A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10R A Preston, J C Post, B J Keats, et al.
Pageof 4