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

M R Eccles

Showing results (21-30 of 46) with videos related to

Pageof 5
Sort By:
Clinical Genetics|May 1, 1997
Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologiesR P Erickson, J F Stone, L A McNoe, et al.
Oncogene|July 1, 1994
Cloning of novel Wilms tumor gene (WT1) cDNAs; evidence for antisense transcription of WT1M R Eccles, G Grubb, O Ogawa, et al.
Lancet (London, England)|January 25, 1992
Trans-sensing hypothesis for origin of Beckwith-Wiedemann syndromeA E Fidler, M A Maw, M R Eccles, et al.
Human Molecular Genetics|November 1, 1995
Mutation of PAX2 in two siblings with renal-coloboma syndromeP Sanyanusin, L A McNoe, M J Sullivan, et al.
Human Molecular Genetics|December 1, 1993
Human insulin-like growth factor type I and type II receptors are not imprintedO Ogawa, L A McNoe, M R Eccles, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 1, 1994
Expression of WT1 protein in fetal kidneys and Wilms tumorsG R Grubb, K Yun, B R Williams, et al.
Nature|September 19, 1985
Expression of insulin-like growth factor-II transcripts in Wilms' tumourA E Reeve, M R Eccles, R J Wilkins, et al.
Oncogene|June 5, 1997
Differential regulation of the human Wilms tumour suppressor gene (WT1) promoter by two isoforms of PAX2M J McConnell, H E Cunliffe, L J Chua, et al.
New Zealand Veterinary Journal|October 13, 2005
Congenital polycystic kidney disease in lambsA C Johnstone, B I Davidson, A R Roe, et al.
Journal of Medical Genetics|May 23, 1998
Absence of PAX2 gene mutations in patients with primary familial vesicoureteric refluxK L Choi, L A McNoe, M C French, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Clinical Genetics|May 1, 1997
Molecular and clinical studies of three cases of female pseudohermaphroditism with caudal dysplasia suggest multiple etiologiesR P Erickson, J F Stone, L A McNoe, et al.
Oncogene|July 1, 1994
Cloning of novel Wilms tumor gene (WT1) cDNAs; evidence for antisense transcription of WT1M R Eccles, G Grubb, O Ogawa, et al.
Lancet (London, England)|January 25, 1992
Trans-sensing hypothesis for origin of Beckwith-Wiedemann syndromeA E Fidler, M A Maw, M R Eccles, et al.
Human Molecular Genetics|November 1, 1995
Mutation of PAX2 in two siblings with renal-coloboma syndromeP Sanyanusin, L A McNoe, M J Sullivan, et al.
Human Molecular Genetics|December 1, 1993
Human insulin-like growth factor type I and type II receptors are not imprintedO Ogawa, L A McNoe, M R Eccles, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 1, 1994
Expression of WT1 protein in fetal kidneys and Wilms tumorsG R Grubb, K Yun, B R Williams, et al.
Nature|September 19, 1985
Expression of insulin-like growth factor-II transcripts in Wilms' tumourA E Reeve, M R Eccles, R J Wilkins, et al.
Oncogene|June 5, 1997
Differential regulation of the human Wilms tumour suppressor gene (WT1) promoter by two isoforms of PAX2M J McConnell, H E Cunliffe, L J Chua, et al.
New Zealand Veterinary Journal|October 13, 2005
Congenital polycystic kidney disease in lambsA C Johnstone, B I Davidson, A R Roe, et al.
Journal of Medical Genetics|May 23, 1998
Absence of PAX2 gene mutations in patients with primary familial vesicoureteric refluxK L Choi, L A McNoe, M C French, et al.
Pageof 5