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 Tayebi

Showing results (11-20 of 31) with videos related to

Pageof 4
Sort By:
Genome Research|October 23, 1997
Identification of three additional genes contiguous to the glucocerebrosidase locus on chromosome 1q21: implications for Gaucher diseaseS L Winfield, N Tayebi, B M Martin, et al.
Clinical Genetics|May 23, 2009
Glucocerebrosidase mutation H255Q appears to be exclusively in cis with D409H: structural implicationsJ Vithayathil, G Gibney, A D Baxevanis, et al.
Clinical Genetics|April 16, 2003
Glucocerebrosidase mutation T369M appears to be another polymorphismJ M Walker, A Lwin, N Tayebi, et al.
The Journal of Biological Chemistry|November 15, 1996
cDNA cloning and characterization of the human interleukin 13 receptor alpha chainM J Aman, N Tayebi, N I Obiri, et al.
American Journal of Medical Genetics|March 10, 2001
Glucocerebrosidase mutations among African-American patients with type 1 Gaucher diseaseJ K Park, V Koprivica, D Q Andrews, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|February 24, 2000
Type 2 Gaucher disease: the collodion baby phenotype revisitedD L Stone, W F Carey, J Christodoulou, et al.
Molecular Genetics and Metabolism|August 18, 2001
Gaucher disease and parkinsonism: a phenotypic and genotypic characterizationN Tayebi, M Callahan, V Madike, et al.
Pediatric Research|May 19, 1998
Genotypic heterogeneity and phenotypic variation among patients with type 2 Gaucher's diseaseN Tayebi, K J Reissner, E K Lau, et al.
American Journal of Human Genetics|May 5, 2000
Analysis and classification of 304 mutant alleles in patients with type 1 and type 3 Gaucher diseaseV Koprivica, D L Stone, J K Park, et al.
Clinical Genetics|March 21, 2002
The E326K mutation and Gaucher disease: mutation or polymorphism?J K Park, N Tayebi, B K Stubblefield, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Genome Research|October 23, 1997
Identification of three additional genes contiguous to the glucocerebrosidase locus on chromosome 1q21: implications for Gaucher diseaseS L Winfield, N Tayebi, B M Martin, et al.
Clinical Genetics|May 23, 2009
Glucocerebrosidase mutation H255Q appears to be exclusively in cis with D409H: structural implicationsJ Vithayathil, G Gibney, A D Baxevanis, et al.
Clinical Genetics|April 16, 2003
Glucocerebrosidase mutation T369M appears to be another polymorphismJ M Walker, A Lwin, N Tayebi, et al.
The Journal of Biological Chemistry|November 15, 1996
cDNA cloning and characterization of the human interleukin 13 receptor alpha chainM J Aman, N Tayebi, N I Obiri, et al.
American Journal of Medical Genetics|March 10, 2001
Glucocerebrosidase mutations among African-American patients with type 1 Gaucher diseaseJ K Park, V Koprivica, D Q Andrews, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|February 24, 2000
Type 2 Gaucher disease: the collodion baby phenotype revisitedD L Stone, W F Carey, J Christodoulou, et al.
Molecular Genetics and Metabolism|August 18, 2001
Gaucher disease and parkinsonism: a phenotypic and genotypic characterizationN Tayebi, M Callahan, V Madike, et al.
Pediatric Research|May 19, 1998
Genotypic heterogeneity and phenotypic variation among patients with type 2 Gaucher's diseaseN Tayebi, K J Reissner, E K Lau, et al.
American Journal of Human Genetics|May 5, 2000
Analysis and classification of 304 mutant alleles in patients with type 1 and type 3 Gaucher diseaseV Koprivica, D L Stone, J K Park, et al.
Clinical Genetics|March 21, 2002
The E326K mutation and Gaucher disease: mutation or polymorphism?J K Park, N Tayebi, B K Stubblefield, et al.
Pageof 4