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C Eng

Showing results (301-310 of 385) with videos related to

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European Journal of Human Genetics : EJHG|July 1, 1997
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung diseaseC Bidaud, R Salomon, G Van Camp, et al.
Oncogene|June 10, 1998
PTEN mutations in gliomas and glioneuronal tumorsE M Duerr, B Rollbrocker, Y Hayashi, et al.
Journal of Medical Genetics|December 1, 1995
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomasC Eng, P A Crossey, L M Mulligan, et al.
Nature|June 3, 1993
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2AL M Mulligan, J B Kwok, C S Healey, et al.
Human Molecular Genetics|February 1, 1994
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumoursC Eng, D P Smith, L M Mulligan, et al.
Oncogene|December 26, 2001
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumoursD Astuti, A Agathanggelou, S Honorio, et al.
The American Journal of Pathology|October 9, 1999
Immunohistochemical evidence of loss of PTEN expression in primary ductal adenocarcinomas of the breastA Perren, L P Weng, A H Boag, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 10, 2011
Systemic chemotherapy and surgical cytoreduction for poorly differentiated and signet ring cell adenocarcinomas of the appendixC H Lieu, L A Lambert, R A Wolff, et al.
Journal of Medical Genetics|April 5, 2005
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutationsM G Butler, M J Dasouki, X-P Zhou, et al.
Journal of Medical Genetics|August 3, 2001
VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortalityB U Bender, C Eng, M Olschewski, et al.
Pageof 39

Showing results (301-310 of 385) with videos related to

Sort By:
Pageof 39
European Journal of Human Genetics : EJHG|July 1, 1997
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung diseaseC Bidaud, R Salomon, G Van Camp, et al.
Oncogene|June 10, 1998
PTEN mutations in gliomas and glioneuronal tumorsE M Duerr, B Rollbrocker, Y Hayashi, et al.
Journal of Medical Genetics|December 1, 1995
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomasC Eng, P A Crossey, L M Mulligan, et al.
Nature|June 3, 1993
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2AL M Mulligan, J B Kwok, C S Healey, et al.
Human Molecular Genetics|February 1, 1994
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumoursC Eng, D P Smith, L M Mulligan, et al.
Oncogene|December 26, 2001
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumoursD Astuti, A Agathanggelou, S Honorio, et al.
The American Journal of Pathology|October 9, 1999
Immunohistochemical evidence of loss of PTEN expression in primary ductal adenocarcinomas of the breastA Perren, L P Weng, A H Boag, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 10, 2011
Systemic chemotherapy and surgical cytoreduction for poorly differentiated and signet ring cell adenocarcinomas of the appendixC H Lieu, L A Lambert, R A Wolff, et al.
Journal of Medical Genetics|April 5, 2005
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutationsM G Butler, M J Dasouki, X-P Zhou, et al.
Journal of Medical Genetics|August 3, 2001
VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortalityB U Bender, C Eng, M Olschewski, et al.
Pageof 39