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Shirley Hodgson

Showing results (21-30 of 73) with videos related to

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Molecular Endocrinology (Baltimore, Md.)|February 14, 2006
A novel activating mutation in the RET tyrosine kinase domain mediates neoplastic transformationAaron Cranston, Cristiana Carniti, Sam Martin, et al.
International Journal of Radiation Biology|March 16, 2007
Is chromosome radiosensitivity and apoptotic response to irradiation correlated with cancer susceptibility?Zoe Docherty, Anne Georgiou, Caroline Langman, et al.
Journal of Molecular Endocrinology|October 20, 2010
No evidence of RET germline mutations in familial pituitary adenomaElina Heliövaara, Sari Tuupanen, Manuel Ahlsten, et al.
Human Mutation|September 4, 2013
UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor geneNaomi C Wake, Christopher J Ricketts, Mark R Morris, et al.
BMC Genomics|March 19, 2005
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndromeNicholas C M Hearle, Ian Tomlinson, Wendy Lim, et al.
Cancer Research|October 19, 2006
RET is constitutively activated by novel tandem mutations that alter the active site resulting in multiple endocrine neoplasia type 2BAaron N Cranston, Cristiana Carniti, Kim Oakhill, et al.
Cancer Research|February 3, 2006
Mammographic density and breast cancer risk in BRCA1 and BRCA2 mutation carriersGillian Mitchell, Antonis C Antoniou, Ruth Warren, et al.
The Journal of Clinical Endocrinology and Metabolism|July 17, 2008
Large genomic deletions in AIP in pituitary adenoma predispositionMarianthi Georgitsi, Elina Heliövaara, Ralf Paschke, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new casesSahar Mansour, Fiona Connell, Colin Steward, et al.
Oncogene|April 11, 2003
Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial casesPäivi Laiho, Tuija Hienonen, Auli Karhu, et al.
Pageof 8

Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
Molecular Endocrinology (Baltimore, Md.)|February 14, 2006
A novel activating mutation in the RET tyrosine kinase domain mediates neoplastic transformationAaron Cranston, Cristiana Carniti, Sam Martin, et al.
International Journal of Radiation Biology|March 16, 2007
Is chromosome radiosensitivity and apoptotic response to irradiation correlated with cancer susceptibility?Zoe Docherty, Anne Georgiou, Caroline Langman, et al.
Journal of Molecular Endocrinology|October 20, 2010
No evidence of RET germline mutations in familial pituitary adenomaElina Heliövaara, Sari Tuupanen, Manuel Ahlsten, et al.
Human Mutation|September 4, 2013
UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor geneNaomi C Wake, Christopher J Ricketts, Mark R Morris, et al.
BMC Genomics|March 19, 2005
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndromeNicholas C M Hearle, Ian Tomlinson, Wendy Lim, et al.
Cancer Research|October 19, 2006
RET is constitutively activated by novel tandem mutations that alter the active site resulting in multiple endocrine neoplasia type 2BAaron N Cranston, Cristiana Carniti, Kim Oakhill, et al.
Cancer Research|February 3, 2006
Mammographic density and breast cancer risk in BRCA1 and BRCA2 mutation carriersGillian Mitchell, Antonis C Antoniou, Ruth Warren, et al.
The Journal of Clinical Endocrinology and Metabolism|July 17, 2008
Large genomic deletions in AIP in pituitary adenoma predispositionMarianthi Georgitsi, Elina Heliövaara, Ralf Paschke, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new casesSahar Mansour, Fiona Connell, Colin Steward, et al.
Oncogene|April 11, 2003
Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial casesPäivi Laiho, Tuija Hienonen, Auli Karhu, et al.
Pageof 8