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Laura E Thomas

Showing results (41-50 of 49) with videos related to

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Human Mutation|April 14, 2025
Targeted Genomic Sequencing of <i>TSC1</i> and <i>TSC2</i> Reveals Causal Variants in Individuals for Whom Previous Genetic Testing for Tuberous Sclerosis Complex Was NormalHannah D West, Mark Nellist, Rutger W W Brouwer, et al.
Molecular Cancer Research : MCR|March 28, 2024
PIGA Mutations and Glycosylphosphatidylinositol Anchor Dysregulation in Polyposis-Associated Duodenal TumorigenesisElena Meuser, Kyle Chang, Angharad Walters, et al.
Nature Communications|July 8, 2022
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cellsPhilip S Robinson, Laura E Thomas, Federico Abascal, et al.
Gastroenterology|November 1, 2020
Duodenal Adenomas and Cancer in MUTYH-associated Polyposis: An International Cohort Study, Laura E Thomas, Joanna J Hurley, et al.
Psychonomic Bulletin & Review|November 10, 2021
A pre-registered, multi-lab non-replication of the action-sentence compatibility effect (ACE)Richard D Morey, Michael P Kaschak, Antonio M Díez-Álamo, et al.
Cell|January 26, 2021
G3BPs tether the TSC complex to lysosomes and suppress mTORC1 signalingMirja Tamara Prentzell, Ulrike Rehbein, Marti Cadena Sandoval, et al.
Hereditary Cancer in Clinical Practice|October 11, 2023
Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statementPal Møller, Toni T Seppälä, Aysel Ahadova, et al.
Medrxiv : the Preprint Server for Health Sciences|March 18, 2026
Familial medullary thyroid carcinoma secondary to an <i>SLC30A9</i> intragenic deletion and translation reinitiationDonato Iacovazzo, Federica Begalli, Oniz Suleyman, et al.
American Journal of Human Genetics|April 23, 2022
Germline MBD4 deficiency causes a multi-tumor predisposition syndromeClaire Palles, Hannah D West, Edward Chew, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Human Mutation|April 14, 2025
Targeted Genomic Sequencing of <i>TSC1</i> and <i>TSC2</i> Reveals Causal Variants in Individuals for Whom Previous Genetic Testing for Tuberous Sclerosis Complex Was NormalHannah D West, Mark Nellist, Rutger W W Brouwer, et al.
Molecular Cancer Research : MCR|March 28, 2024
PIGA Mutations and Glycosylphosphatidylinositol Anchor Dysregulation in Polyposis-Associated Duodenal TumorigenesisElena Meuser, Kyle Chang, Angharad Walters, et al.
Nature Communications|July 8, 2022
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cellsPhilip S Robinson, Laura E Thomas, Federico Abascal, et al.
Gastroenterology|November 1, 2020
Duodenal Adenomas and Cancer in MUTYH-associated Polyposis: An International Cohort Study, Laura E Thomas, Joanna J Hurley, et al.
Psychonomic Bulletin & Review|November 10, 2021
A pre-registered, multi-lab non-replication of the action-sentence compatibility effect (ACE)Richard D Morey, Michael P Kaschak, Antonio M Díez-Álamo, et al.
Cell|January 26, 2021
G3BPs tether the TSC complex to lysosomes and suppress mTORC1 signalingMirja Tamara Prentzell, Ulrike Rehbein, Marti Cadena Sandoval, et al.
Hereditary Cancer in Clinical Practice|October 11, 2023
Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statementPal Møller, Toni T Seppälä, Aysel Ahadova, et al.
Medrxiv : the Preprint Server for Health Sciences|March 18, 2026
Familial medullary thyroid carcinoma secondary to an <i>SLC30A9</i> intragenic deletion and translation reinitiationDonato Iacovazzo, Federica Begalli, Oniz Suleyman, et al.
American Journal of Human Genetics|April 23, 2022
Germline MBD4 deficiency causes a multi-tumor predisposition syndromeClaire Palles, Hannah D West, Edward Chew, et al.
Pageof 5