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R Sampson

Showing results (501-510 of 518) with videos related to

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Gut|July 30, 2017
Cancer risk and survival in <i>path_MMR</i> carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome DatabasePål Møller, Toni T Seppälä, Inge Bernstein, et al.
Journal of Clinical Medicine|July 26, 2020
Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Toni T Seppälä, Christoph Engel, et al.
Hereditary Cancer in Clinical Practice|October 23, 2019
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database reportMev Dominguez-Valentin, Toni T Seppälä, Julian R Sampson, 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.
Aging Cell|March 13, 2026
Biologically Younger Individuals, as Identified by MARK-AGE Biological Age Scores, Display a Distinct Favourable Blood Chemistry Profile Regardless of AgeMaría Moreno-Villanueva, Michael Junk, Grażyna Mosieniak, et al.
Human Mutation|November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesisOlivier Gribouval, Vincent Morinière, Audrey Pawtowski, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2021
Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2020
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
Pageof 52

Showing results (501-510 of 518) with videos related to

Sort By:
Pageof 52
Gut|July 30, 2017
Cancer risk and survival in <i>path_MMR</i> carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome DatabasePål Møller, Toni T Seppälä, Inge Bernstein, et al.
Journal of Clinical Medicine|July 26, 2020
Risk-Reducing Gynecological Surgery in Lynch Syndrome: Results of an International Survey from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Toni T Seppälä, Christoph Engel, et al.
Hereditary Cancer in Clinical Practice|October 23, 2019
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database reportMev Dominguez-Valentin, Toni T Seppälä, Julian R Sampson, 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.
Aging Cell|March 13, 2026
Biologically Younger Individuals, as Identified by MARK-AGE Biological Age Scores, Display a Distinct Favourable Blood Chemistry Profile Regardless of AgeMaría Moreno-Villanueva, Michael Junk, Grażyna Mosieniak, et al.
Human Mutation|November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesisOlivier Gribouval, Vincent Morinière, Audrey Pawtowski, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 9, 2021
Correction to: De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 10, 2020
De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathyChiara Klöckner, Heinrich Sticht, Pia Zacher, et al.
Pageof 52