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

C A Warner

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Medical Laboratory Sciences|July 1, 1989
Screening for cervical carcinomaC A Warner, D J McCance
The Journal of Clinical Investigation|February 1, 1995
Congenital erythropoietic porphyria: identification and expression of 10 mutations in the uroporphyrinogen III synthase geneW Xu, C A Warner, R J Desnick
Arthritis and Rheumatism|August 1, 1988
DQ beta polymorphism and genetic susceptibility to Felty's syndromeA K So, C A Warner, D Sansom, et al.
The Journal of Rheumatology|April 1, 1992
Subcutaneous pancreatic fat necrosis associated with acute arthritisK G Saag, T H Niemann, C A Warner, et al.
Genomics|January 1, 1993
Hydroxymethylbilane synthase: complete genomic sequence and amplifiable polymorphisms in the human geneH W Yoo, C A Warner, C H Chen, et al.
The Journal of Clinical Investigation|February 1, 1992
Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase geneC A Warner, H W Yoo, A G Roberts, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 30, 1998
Senescent BALB/c mice exhibit decreased expression of lambda5 surrogate light chains and reduced development within the pre-B cell compartmentE M Sherwood, B B Blomberg, W Xu, et al.
Clinical Endocrinology|June 1, 1988
Immunogenetics of Graves' ophthalmopathyA P Weetman, A K So, C A Warner, et al.
Archives of Dermatology|September 1, 1992
Congenital erythropoietic porphyria. A mild variant with low uroporphyrin I levels due to a missense mutation (A66V) encoding residual uroporphyrinogen III synthase activityC A Warner, M B Poh-Fitzpatrick, E F Zaider, et al.
Human Genetics|May 1, 1991
Regional assignment of the human uroporphyrinogen III synthase (UROS) gene to chromosome 10q25.2----q26.3K H Astrin, C A Warner, H W Yoo, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Medical Laboratory Sciences|July 1, 1989
Screening for cervical carcinomaC A Warner, D J McCance
The Journal of Clinical Investigation|February 1, 1995
Congenital erythropoietic porphyria: identification and expression of 10 mutations in the uroporphyrinogen III synthase geneW Xu, C A Warner, R J Desnick
Arthritis and Rheumatism|August 1, 1988
DQ beta polymorphism and genetic susceptibility to Felty's syndromeA K So, C A Warner, D Sansom, et al.
The Journal of Rheumatology|April 1, 1992
Subcutaneous pancreatic fat necrosis associated with acute arthritisK G Saag, T H Niemann, C A Warner, et al.
Genomics|January 1, 1993
Hydroxymethylbilane synthase: complete genomic sequence and amplifiable polymorphisms in the human geneH W Yoo, C A Warner, C H Chen, et al.
The Journal of Clinical Investigation|February 1, 1992
Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase geneC A Warner, H W Yoo, A G Roberts, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 30, 1998
Senescent BALB/c mice exhibit decreased expression of lambda5 surrogate light chains and reduced development within the pre-B cell compartmentE M Sherwood, B B Blomberg, W Xu, et al.
Clinical Endocrinology|June 1, 1988
Immunogenetics of Graves' ophthalmopathyA P Weetman, A K So, C A Warner, et al.
Archives of Dermatology|September 1, 1992
Congenital erythropoietic porphyria. A mild variant with low uroporphyrin I levels due to a missense mutation (A66V) encoding residual uroporphyrinogen III synthase activityC A Warner, M B Poh-Fitzpatrick, E F Zaider, et al.
Human Genetics|May 1, 1991
Regional assignment of the human uroporphyrinogen III synthase (UROS) gene to chromosome 10q25.2----q26.3K H Astrin, C A Warner, H W Yoo, et al.
Pageof 2