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C C Morton

Showing results (131-140 of 185) with videos related to

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Genes, Chromosomes & Cancer|September 1, 1994
Analysis of androgen receptor DNA reveals the independent clonal origins of uterine leiomyomata and the secondary nature of cytogenetic aberrations in the development of leiomyomataR D Mashal, M L Fejzo, A J Friedman, et al.
Genomics|January 20, 1995
Homologs of Drosophila Fushi-Tarazu factor 1 map to mouse chromosome 2 and human chromosome 9q33M Taketo, K L Parker, T A Howard, et al.
The Journal of Clinical Investigation|June 1, 1995
Expression of two human skeletal calcitonin receptor isoforms cloned from a giant cell tumor of bone. The first intracellular domain modulates ligand binding and signal transductionA H Gorn, S M Rudolph, M R Flannery, et al.
Biochemical and Biophysical Research Communications|December 1, 2000
Human calcium transport protein CaT1J B Peng, X Z Chen, U V Berger, et al.
American Journal of Human Genetics|October 1, 1988
Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21M C Phelan, C C Morton, R E Stevenson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 27, 2001
Genomic structure, functional comparison, and tissue distribution of mouse Cd59a and Cd59bX Qin, T Miwa, H Aktas, et al.
Human Molecular Genetics|August 1, 1997
Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer miceK B Avraham, T Hasson, T Sobe, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1987
The gene encoding the epsilon subunit of the T3/T-cell receptor complex maps to chromosome 11 in humans and to chromosome 9 in miceD P Gold, J J van Dongen, C C Morton, et al.
The Journal of Clinical Investigation|September 7, 2000
Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complexM Casey, C J Vaughan, J He, et al.
Genomics|January 27, 1998
Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9N G Robertson, A B Skvorak, Y Yin, et al.
Pageof 19

Showing results (131-140 of 185) with videos related to

Sort By:
Pageof 19
Genes, Chromosomes & Cancer|September 1, 1994
Analysis of androgen receptor DNA reveals the independent clonal origins of uterine leiomyomata and the secondary nature of cytogenetic aberrations in the development of leiomyomataR D Mashal, M L Fejzo, A J Friedman, et al.
Genomics|January 20, 1995
Homologs of Drosophila Fushi-Tarazu factor 1 map to mouse chromosome 2 and human chromosome 9q33M Taketo, K L Parker, T A Howard, et al.
The Journal of Clinical Investigation|June 1, 1995
Expression of two human skeletal calcitonin receptor isoforms cloned from a giant cell tumor of bone. The first intracellular domain modulates ligand binding and signal transductionA H Gorn, S M Rudolph, M R Flannery, et al.
Biochemical and Biophysical Research Communications|December 1, 2000
Human calcium transport protein CaT1J B Peng, X Z Chen, U V Berger, et al.
American Journal of Human Genetics|October 1, 1988
Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21M C Phelan, C C Morton, R E Stevenson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 27, 2001
Genomic structure, functional comparison, and tissue distribution of mouse Cd59a and Cd59bX Qin, T Miwa, H Aktas, et al.
Human Molecular Genetics|August 1, 1997
Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer miceK B Avraham, T Hasson, T Sobe, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1987
The gene encoding the epsilon subunit of the T3/T-cell receptor complex maps to chromosome 11 in humans and to chromosome 9 in miceD P Gold, J J van Dongen, C C Morton, et al.
The Journal of Clinical Investigation|September 7, 2000
Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complexM Casey, C J Vaughan, J He, et al.
Genomics|January 27, 1998
Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9N G Robertson, A B Skvorak, Y Yin, et al.
Pageof 19