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E L Duncan

Showing results (11-20 of 24) with videos related to

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Molecular Biotechnology|November 20, 1998
Differential display of mRNAJ S Zhang, E L Duncan, A C Chang, et al.
Oncogene|October 21, 1998
Malignant transformation of NIH3T3 cells by overexpression of mot-2 proteinS C Kaul, E L Duncan, A Englezou, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Suggestive linkage of the parathyroid receptor type 1 to osteoporosisE L Duncan, M A Brown, J Sinsheimer, et al.
The Journal of Biological Chemistry|May 18, 1999
Cloning and characterization of a novel gene, striamin, that interacts with the tumor suppressor protein p53R Wadhwa, T Sugihara, A Yoshida, et al.
Human Molecular Genetics|November 5, 1997
Isolation of a candidate human telomerase catalytic subunit gene, which reveals complex splicing patterns in different cell typesA Kilian, D D Bowtell, H E Abud, et al.
Clinical Genetics|June 4, 2014
COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?A M McInerney-Leo, E L Duncan, P J Leo, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|July 9, 2011
Risedronate in adults with osteogenesis imperfecta type I: increased bone mineral density and decreased bone turnover, but high fracture rate persistsL A Bradbury, S Barlow, F Geoghegan, et al.
International Journal of Cancer|April 10, 1995
SV40-induced immortalization and ras-transformation of human bronchial epithelial cellsR R Reddel, R De Silva, E L Duncan, et al.
Pediatric Diabetes|February 9, 2018
Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinismS R Johnson, P J Leo, A M McInerney-Leo, et al.
The British Journal of Dermatology|December 27, 2017
Point mutation in p14<sup>ARF</sup> -specific exon 1β of CDKN2A causing familial melanoma and astrocytomaA M McInerney-Leo, L Wheeler, R A Sturm, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Molecular Biotechnology|November 20, 1998
Differential display of mRNAJ S Zhang, E L Duncan, A C Chang, et al.
Oncogene|October 21, 1998
Malignant transformation of NIH3T3 cells by overexpression of mot-2 proteinS C Kaul, E L Duncan, A Englezou, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Suggestive linkage of the parathyroid receptor type 1 to osteoporosisE L Duncan, M A Brown, J Sinsheimer, et al.
The Journal of Biological Chemistry|May 18, 1999
Cloning and characterization of a novel gene, striamin, that interacts with the tumor suppressor protein p53R Wadhwa, T Sugihara, A Yoshida, et al.
Human Molecular Genetics|November 5, 1997
Isolation of a candidate human telomerase catalytic subunit gene, which reveals complex splicing patterns in different cell typesA Kilian, D D Bowtell, H E Abud, et al.
Clinical Genetics|June 4, 2014
COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?A M McInerney-Leo, E L Duncan, P J Leo, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|July 9, 2011
Risedronate in adults with osteogenesis imperfecta type I: increased bone mineral density and decreased bone turnover, but high fracture rate persistsL A Bradbury, S Barlow, F Geoghegan, et al.
International Journal of Cancer|April 10, 1995
SV40-induced immortalization and ras-transformation of human bronchial epithelial cellsR R Reddel, R De Silva, E L Duncan, et al.
Pediatric Diabetes|February 9, 2018
Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinismS R Johnson, P J Leo, A M McInerney-Leo, et al.
The British Journal of Dermatology|December 27, 2017
Point mutation in p14<sup>ARF</sup> -specific exon 1β of CDKN2A causing familial melanoma and astrocytomaA M McInerney-Leo, L Wheeler, R A Sturm, et al.
Pageof 3