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Beverley Anderson

Showing results (21-30 of 33) with videos related to

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British Journal of Nursing (Mark Allen Publishing)|October 30, 2016
Prostate cancer among Jamaican men: exploring the evidence for higher riskBeverley Anderson, Sylvie Marshall-Lucette
Cancer Treatment Reviews|December 10, 2002
Management of the menopause in cancer survivorsMark Clemons, Andrew Clamp, Beverley Anderson
Conservation Biology : the Journal of the Society for Conservation Biology|October 22, 2009
Collaborative planning fosters multiple-benefit restoration projects on the Sacramento RiverGregory H Golet, Beverley Anderson, Ryan A Luster, et al.
Scientific Reports|June 9, 2016
Tumour Suppressor Adenomatous Polyposis Coli (APC) localisation is regulated by both Kinesin-1 and Kinesin-2Peter T Ruane, Laura F Gumy, Becky Bola, et al.
Molecular Syndromology|October 23, 2014
Exome Sequencing Identifies a Dominant TNNT3 Mutation in a Large Family with Distal ArthrogryposisSarah B Daly, Hitesh Shah, James O'Sullivan, et al.
Ophthalmology|August 3, 2015
Next-generation Sequencing in the Diagnosis of Metabolic Disease Marked by Pediatric CataractRachel L Gillespie, Jill Urquhart, Beverley Anderson, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 19, 2014
Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutationsMiriam J Smith, Christian Beetz, Simon G Williams, et al.
American Journal of Human Genetics|December 27, 2011
Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locusKaren Mitchell, James O'Sullivan, Caterina Missero, et al.
Nature Communications|May 26, 2026
Paired DNA and RNA sequencing uncovers common and rare variation regulating human retinal gene expressionJacob Sampson, Ayellet V Segrè, Kinga M Bujakowska, et al.
American Journal of Human Genetics|November 15, 2011
Whole-exome-sequencing identifies mutations in histone acetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variant of Ohdo syndromeJill Clayton-Smith, James O'Sullivan, Sarah Daly, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
British Journal of Nursing (Mark Allen Publishing)|October 30, 2016
Prostate cancer among Jamaican men: exploring the evidence for higher riskBeverley Anderson, Sylvie Marshall-Lucette
Cancer Treatment Reviews|December 10, 2002
Management of the menopause in cancer survivorsMark Clemons, Andrew Clamp, Beverley Anderson
Conservation Biology : the Journal of the Society for Conservation Biology|October 22, 2009
Collaborative planning fosters multiple-benefit restoration projects on the Sacramento RiverGregory H Golet, Beverley Anderson, Ryan A Luster, et al.
Scientific Reports|June 9, 2016
Tumour Suppressor Adenomatous Polyposis Coli (APC) localisation is regulated by both Kinesin-1 and Kinesin-2Peter T Ruane, Laura F Gumy, Becky Bola, et al.
Molecular Syndromology|October 23, 2014
Exome Sequencing Identifies a Dominant TNNT3 Mutation in a Large Family with Distal ArthrogryposisSarah B Daly, Hitesh Shah, James O'Sullivan, et al.
Ophthalmology|August 3, 2015
Next-generation Sequencing in the Diagnosis of Metabolic Disease Marked by Pediatric CataractRachel L Gillespie, Jill Urquhart, Beverley Anderson, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 19, 2014
Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutationsMiriam J Smith, Christian Beetz, Simon G Williams, et al.
American Journal of Human Genetics|December 27, 2011
Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locusKaren Mitchell, James O'Sullivan, Caterina Missero, et al.
Nature Communications|May 26, 2026
Paired DNA and RNA sequencing uncovers common and rare variation regulating human retinal gene expressionJacob Sampson, Ayellet V Segrè, Kinga M Bujakowska, et al.
American Journal of Human Genetics|November 15, 2011
Whole-exome-sequencing identifies mutations in histone acetyltransferase gene KAT6B in individuals with the Say-Barber-Biesecker variant of Ohdo syndromeJill Clayton-Smith, James O'Sullivan, Sarah Daly, et al.
Pageof 4