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 P Carter

Showing results (41-50 of 103) with videos related to

Pageof 11
Sort By:
Transplantation Proceedings|February 1, 1989
The diagnosis of renal allograft rejection: an improved assessment of graft infiltration using image analysisR A Foot, S V Fuggle, D L McWhinnie, et al.
The New England Journal of Medicine|May 6, 1982
Role of T-cell-subset monitoring in renal-allograft recipientsP J Morris, N P Carter, P R Cullen, et al.
Cytometry|January 1, 1993
Chromatid contamination can impair the purity of flow-sorted metaphase chromosomesH Telenius, D de Vos, E Blennow, et al.
Cytometry|January 1, 1990
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blotsN P Carter, M E Ferguson-Smith, N A Affara, et al.
Cancer Genetics and Cytogenetics|May 29, 1999
Elucidation of the mechanism of homozygous deletion of 3p12-13 in the U2020 cell line reveals the unexpected involvement of other chromosomesA C Heppell-Parton, E Nacheva, N P Carter, et al.
Transplantation Proceedings|February 1, 1989
Immunohistology or conventional histology for the diagnosis of renal allograft rejection?D L McWhinnie, D Hughes, S V Fuggle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
Characterization of the mouse beta-prime adaptin gene; cDNA sequence, genomic structure, and chromosomal localizationC Guilbaud, M Peyrard, I Fransson, et al.
Atherosclerosis|January 25, 1993
Flow cytometric measurement of ceroid accumulation in macrophagesJ V Hunt, K L Carpenter, M A Bottoms, et al.
Genomics|December 1, 1991
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22D M Whitcombe, N P Carter, D G Albertson, et al.
American Journal of Medical Genetics|January 2, 1995
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridizationE Blennow, K B Nielsen, H Telenius, et al.
Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:
Pageof 11
Transplantation Proceedings|February 1, 1989
The diagnosis of renal allograft rejection: an improved assessment of graft infiltration using image analysisR A Foot, S V Fuggle, D L McWhinnie, et al.
The New England Journal of Medicine|May 6, 1982
Role of T-cell-subset monitoring in renal-allograft recipientsP J Morris, N P Carter, P R Cullen, et al.
Cytometry|January 1, 1993
Chromatid contamination can impair the purity of flow-sorted metaphase chromosomesH Telenius, D de Vos, E Blennow, et al.
Cytometry|January 1, 1990
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blotsN P Carter, M E Ferguson-Smith, N A Affara, et al.
Cancer Genetics and Cytogenetics|May 29, 1999
Elucidation of the mechanism of homozygous deletion of 3p12-13 in the U2020 cell line reveals the unexpected involvement of other chromosomesA C Heppell-Parton, E Nacheva, N P Carter, et al.
Transplantation Proceedings|February 1, 1989
Immunohistology or conventional histology for the diagnosis of renal allograft rejection?D L McWhinnie, D Hughes, S V Fuggle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
Characterization of the mouse beta-prime adaptin gene; cDNA sequence, genomic structure, and chromosomal localizationC Guilbaud, M Peyrard, I Fransson, et al.
Atherosclerosis|January 25, 1993
Flow cytometric measurement of ceroid accumulation in macrophagesJ V Hunt, K L Carpenter, M A Bottoms, et al.
Genomics|December 1, 1991
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22D M Whitcombe, N P Carter, D G Albertson, et al.
American Journal of Medical Genetics|January 2, 1995
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridizationE Blennow, K B Nielsen, H Telenius, et al.
Pageof 11