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John Burn

Showing results (91-100 of 162) with videos related to

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Nature Genetics|July 26, 2003
Identification of Stk6/STK15 as a candidate low-penetrance tumor-susceptibility gene in mouse and humanAmanda Ewart-Toland, Paraskevi Briassouli, John P de Koning, et al.
European Journal of Human Genetics : EJHG|February 15, 2024
Identification of people with Lynch syndrome from those presenting with colorectal cancer in England: baseline analysis of the diagnostic pathwayFiona E McRonald, Joanna Pethick, Francesco Santaniello, et al.
Journal of Genetic Counseling|August 7, 2025
Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview studyKelly Kohut, Kate Morton, Lesley Turner, et al.
Journal of the American Academy of Dermatology|April 9, 2023
Sebaceous carcinoma epidemiology, associated malignancies and Lynch/Muir-Torre syndrome screening in England from 2008 to 2018Sam Cook, Joanna Pethick, Nour Kibbi, et al.
Leukemia & Lymphoma|October 22, 2022
Detection of constitutional mismatch repair deficiency in children and adolescents with acute lymphoblastic leukemiaRichard Gallon, Rachel Phelps, Leigh Betts, et al.
Eclinicalmedicine|February 15, 2024
The comprehensive English National Lynch Syndrome Registry: development and description of a new genomics data resourceCatherine Huntley, Lucy Loong, Corinne Mallinson, et al.
Cancers|December 17, 2024
Detection of Mismatch Repair Deficiency in Endometrial Cancer: Assessment of IHC, Fragment Length Analysis, and Amplicon Sequencing Based MSI TestingPeter Sowter, Richard Gallon, Christine Hayes, et al.
Ebiomedicine|October 25, 2025
Detection of urothelial carcinoma in Lynch syndrome using microsatellite instability analysis of urine cell-free DNARebecca Hall, Richard Gallon, Christine Hayes, et al.
Plos One|August 30, 2018
A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumoursLisa Redford, Ghanim Alhilal, Stephanie Needham, et al.
JAMA Dermatology|June 30, 2018
Targeting Tropomyosin Receptor Kinase in Cutaneous CYLD Defective Tumors With Pegcantratinib: The TRAC Randomized Clinical TrialMarina Danilenko, Elaine Stamp, Deborah D Stocken, et al.
Pageof 17

Showing results (91-100 of 162) with videos related to

Sort By:
Pageof 17
Nature Genetics|July 26, 2003
Identification of Stk6/STK15 as a candidate low-penetrance tumor-susceptibility gene in mouse and humanAmanda Ewart-Toland, Paraskevi Briassouli, John P de Koning, et al.
European Journal of Human Genetics : EJHG|February 15, 2024
Identification of people with Lynch syndrome from those presenting with colorectal cancer in England: baseline analysis of the diagnostic pathwayFiona E McRonald, Joanna Pethick, Francesco Santaniello, et al.
Journal of Genetic Counseling|August 7, 2025
Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview studyKelly Kohut, Kate Morton, Lesley Turner, et al.
Journal of the American Academy of Dermatology|April 9, 2023
Sebaceous carcinoma epidemiology, associated malignancies and Lynch/Muir-Torre syndrome screening in England from 2008 to 2018Sam Cook, Joanna Pethick, Nour Kibbi, et al.
Leukemia & Lymphoma|October 22, 2022
Detection of constitutional mismatch repair deficiency in children and adolescents with acute lymphoblastic leukemiaRichard Gallon, Rachel Phelps, Leigh Betts, et al.
Eclinicalmedicine|February 15, 2024
The comprehensive English National Lynch Syndrome Registry: development and description of a new genomics data resourceCatherine Huntley, Lucy Loong, Corinne Mallinson, et al.
Cancers|December 17, 2024
Detection of Mismatch Repair Deficiency in Endometrial Cancer: Assessment of IHC, Fragment Length Analysis, and Amplicon Sequencing Based MSI TestingPeter Sowter, Richard Gallon, Christine Hayes, et al.
Ebiomedicine|October 25, 2025
Detection of urothelial carcinoma in Lynch syndrome using microsatellite instability analysis of urine cell-free DNARebecca Hall, Richard Gallon, Christine Hayes, et al.
Plos One|August 30, 2018
A novel panel of short mononucleotide repeats linked to informative polymorphisms enabling effective high volume low cost discrimination between mismatch repair deficient and proficient tumoursLisa Redford, Ghanim Alhilal, Stephanie Needham, et al.
JAMA Dermatology|June 30, 2018
Targeting Tropomyosin Receptor Kinase in Cutaneous CYLD Defective Tumors With Pegcantratinib: The TRAC Randomized Clinical TrialMarina Danilenko, Elaine Stamp, Deborah D Stocken, et al.
Pageof 17