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E R Maher

Showing results (71-80 of 171) with videos related to

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Journal of Medical Genetics|March 2, 1999
A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancerN J Froggatt, J Green, C Brassett, et al.
Human Molecular Genetics|February 1, 1994
Somatic NF2 gene mutations in familial and non-familial vestibular schwannomaR M Irving, D A Moffat, D G Hardy, et al.
Human Molecular Genetics|July 1, 1997
Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHLE R Woodward, C Eng, R McMahon, et al.
Human Molecular Genetics|December 1, 1996
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathwayK W Brown, A J Villar, W Bickmore, et al.
Oncogene|February 19, 2013
Knockdown of Slingshot 2 (SSH2) serine phosphatase induces Caspase3 activation in human carcinoma cell lines with the loss of the Birt-Hogg-Dubé tumour suppressor gene (FLCN)X Lu, U Boora, L Seabra, et al.
Journal of Medical Genetics|October 1, 1994
Mosaic uniparental disomy in Beckwith-Wiedemann syndromeR E Slatter, M Elliott, K Welham, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 1, 1993
Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuromaR M Irving, D A Moffat, D G Hardy, et al.
Human Molecular Genetics|December 17, 2013
The tumor susceptibility gene TMEM127 is mutated in renal cell carcinomas and modulates endolysosomal functionY Qin, Y Deng, C J Ricketts, et al.
Journal of Medical Genetics|October 3, 1999
Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancerL Verma, M F Kane, C Brassett, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 30, 2000
Renal cancer and malformations in relatives of patients with Bardet-Biedl syndromeP L Beales, H A Reid, M H Griffiths, et al.
Pageof 18

Showing results (71-80 of 171) with videos related to

Sort By:
Pageof 18
Journal of Medical Genetics|March 2, 1999
A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancerN J Froggatt, J Green, C Brassett, et al.
Human Molecular Genetics|February 1, 1994
Somatic NF2 gene mutations in familial and non-familial vestibular schwannomaR M Irving, D A Moffat, D G Hardy, et al.
Human Molecular Genetics|July 1, 1997
Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHLE R Woodward, C Eng, R McMahon, et al.
Human Molecular Genetics|December 1, 1996
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathwayK W Brown, A J Villar, W Bickmore, et al.
Oncogene|February 19, 2013
Knockdown of Slingshot 2 (SSH2) serine phosphatase induces Caspase3 activation in human carcinoma cell lines with the loss of the Birt-Hogg-Dubé tumour suppressor gene (FLCN)X Lu, U Boora, L Seabra, et al.
Journal of Medical Genetics|October 1, 1994
Mosaic uniparental disomy in Beckwith-Wiedemann syndromeR E Slatter, M Elliott, K Welham, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 1, 1993
Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuromaR M Irving, D A Moffat, D G Hardy, et al.
Human Molecular Genetics|December 17, 2013
The tumor susceptibility gene TMEM127 is mutated in renal cell carcinomas and modulates endolysosomal functionY Qin, Y Deng, C J Ricketts, et al.
Journal of Medical Genetics|October 3, 1999
Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancerL Verma, M F Kane, C Brassett, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 30, 2000
Renal cancer and malformations in relatives of patients with Bardet-Biedl syndromeP L Beales, H A Reid, M H Griffiths, et al.
Pageof 18