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

A Corfield

Showing results (51-60 of 64) with videos related to

Pageof 7
Sort By:
Psychiatry Research|October 19, 2004
Early- versus late-onset obsessive-compulsive disorder: investigating genetic and clinical correlatesSîan M J Hemmings, Craig J Kinnear, Christine Lochner, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|March 26, 2003
Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorderSîan M J Hemmings, Craig J Kinnear, Dana J H Niehaus, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|March 12, 2004
Gender in obsessive-compulsive disorder: clinical and genetic findingsChristine Lochner, Sian M J Hemmings, Craig J Kinnear, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|October 8, 2004
Corrigendum to "gender in obsessive-compulsive disorder: clinical and genetic findings" [Eur. Neuropsychopharmacol. 14 (2004) 105-113]Christine Lochner, Sian M J Hemmings, Craig J Kinnear, et al.
Circulation. Cardiovascular Genetics|August 5, 2014
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1Carin P de Villiers, Lize van der Merwe, Lia Crotti, et al.
Comprehensive Psychiatry|February 17, 2005
Cluster analysis of obsessive-compulsive spectrum disorders in patients with obsessive-compulsive disorder: clinical and genetic correlatesChristine Lochner, Sian M J Hemmings, Craig J Kinnear, et al.
Molecular Cell|July 22, 2020
Structure of the Inhibited State of the Sec TransloconSamuel F Gérard, Belinda S Hall, Afroditi M Zaki, et al.
Glycoconjugate Journal|October 1, 1996
Colonic mucins in ulcerative colitis: evidence for loss of sulfationA P Corfield, N Myerscough, N Bradfield, et al.
Journal of Medical Genetics|December 19, 2001
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsP S Andersen, O Havndrup, H Bundgaard, et al.
The International Journal of Neuropsychopharmacology|May 10, 2001
Obsessive-compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner populationCraig J. Kinnear, Dana J. H. Niehaus, Johanna C. Moolman-Smook, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Psychiatry Research|October 19, 2004
Early- versus late-onset obsessive-compulsive disorder: investigating genetic and clinical correlatesSîan M J Hemmings, Craig J Kinnear, Christine Lochner, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|March 26, 2003
Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorderSîan M J Hemmings, Craig J Kinnear, Dana J H Niehaus, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|March 12, 2004
Gender in obsessive-compulsive disorder: clinical and genetic findingsChristine Lochner, Sian M J Hemmings, Craig J Kinnear, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|October 8, 2004
Corrigendum to "gender in obsessive-compulsive disorder: clinical and genetic findings" [Eur. Neuropsychopharmacol. 14 (2004) 105-113]Christine Lochner, Sian M J Hemmings, Craig J Kinnear, et al.
Circulation. Cardiovascular Genetics|August 5, 2014
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1Carin P de Villiers, Lize van der Merwe, Lia Crotti, et al.
Comprehensive Psychiatry|February 17, 2005
Cluster analysis of obsessive-compulsive spectrum disorders in patients with obsessive-compulsive disorder: clinical and genetic correlatesChristine Lochner, Sian M J Hemmings, Craig J Kinnear, et al.
Molecular Cell|July 22, 2020
Structure of the Inhibited State of the Sec TransloconSamuel F Gérard, Belinda S Hall, Afroditi M Zaki, et al.
Glycoconjugate Journal|October 1, 1996
Colonic mucins in ulcerative colitis: evidence for loss of sulfationA P Corfield, N Myerscough, N Bradfield, et al.
Journal of Medical Genetics|December 19, 2001
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsP S Andersen, O Havndrup, H Bundgaard, et al.
The International Journal of Neuropsychopharmacology|May 10, 2001
Obsessive-compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner populationCraig J. Kinnear, Dana J. H. Niehaus, Johanna C. Moolman-Smook, et al.
Pageof 7