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Charis Eng

Showing results (331-340 of 555) with videos related to

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Translational Research : the Journal of Laboratory and Clinical Medicine|June 26, 2007
Consortium approach to identifying genes for Barrett's esophagus and esophageal adenocarcinomaHeather M Ochs-Balcom, Gary Falk, William M Grady, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2012
PTEN lipid phosphatase activity and proper subcellular localization are necessary and sufficient for down-regulating AKT phosphorylation in the nucleus in Cowden syndromeXin He, Motoyasu Saji, Deepa Radhakrishnan, et al.
Thyroid : Official Journal of the American Thyroid Association|March 23, 2011
Frequency of germline PTEN mutations in differentiated thyroid cancerRebecca Nagy, Shireen Ganapathi, Ilene Comeras, et al.
The Journal of Clinical Endocrinology and Metabolism|November 18, 2004
Silencing of the maternally imprinted tumor suppressor ARHI contributes to follicular thyroid carcinogenesisFrank Weber, Micheala A Aldred, Carl D Morrison, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 31, 2009
Squamous morules are functionally inert elements of premalignant endometrial neoplasiaMing-Chieh Lin, Lesley Lomo, Jan P A Baak, et al.
Gynecologic Oncology|April 25, 2013
Implementation of tumor testing for lynch syndrome in endometrial cancers at a large academic medical centerJessica Moline, Haider Mahdi, Bin Yang, et al.
Annals of Surgical Oncology|August 11, 2023
A Randomized Trial Comparing the Effectiveness of Pre-test Genetic Counseling Using an Artificial Intelligence Automated Chatbot and Traditional In-person Genetic Counseling in Women Newly Diagnosed with Breast CancerZahraa Al-Hilli, Ryan Noss, Jennifer Dickard, et al.
The Journal of Clinical Endocrinology and Metabolism|June 22, 2006
Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytomaBirke Bausch, Ann-Cathrin Koschker, Martin Fassnacht, et al.
Breast Cancer Research and Treatment|November 8, 2012
The clinical consequences of hemizygosity across 2 MB of 10q23 are restricted to Cowden syndromeCheryl M Lewis, Dawei Bu, Venetia Sarode, et al.
Human Molecular Genetics|January 29, 2014
Germline disruption of Pten localization causes enhanced sex-dependent social motivation and increased glial productionAmanda K Tilot, Mary K Gaugler, Qi Yu, et al.
Pageof 56

Showing results (331-340 of 555) with videos related to

Sort By:
Pageof 56
Translational Research : the Journal of Laboratory and Clinical Medicine|June 26, 2007
Consortium approach to identifying genes for Barrett's esophagus and esophageal adenocarcinomaHeather M Ochs-Balcom, Gary Falk, William M Grady, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2012
PTEN lipid phosphatase activity and proper subcellular localization are necessary and sufficient for down-regulating AKT phosphorylation in the nucleus in Cowden syndromeXin He, Motoyasu Saji, Deepa Radhakrishnan, et al.
Thyroid : Official Journal of the American Thyroid Association|March 23, 2011
Frequency of germline PTEN mutations in differentiated thyroid cancerRebecca Nagy, Shireen Ganapathi, Ilene Comeras, et al.
The Journal of Clinical Endocrinology and Metabolism|November 18, 2004
Silencing of the maternally imprinted tumor suppressor ARHI contributes to follicular thyroid carcinogenesisFrank Weber, Micheala A Aldred, Carl D Morrison, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 31, 2009
Squamous morules are functionally inert elements of premalignant endometrial neoplasiaMing-Chieh Lin, Lesley Lomo, Jan P A Baak, et al.
Gynecologic Oncology|April 25, 2013
Implementation of tumor testing for lynch syndrome in endometrial cancers at a large academic medical centerJessica Moline, Haider Mahdi, Bin Yang, et al.
Annals of Surgical Oncology|August 11, 2023
A Randomized Trial Comparing the Effectiveness of Pre-test Genetic Counseling Using an Artificial Intelligence Automated Chatbot and Traditional In-person Genetic Counseling in Women Newly Diagnosed with Breast CancerZahraa Al-Hilli, Ryan Noss, Jennifer Dickard, et al.
The Journal of Clinical Endocrinology and Metabolism|June 22, 2006
Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytomaBirke Bausch, Ann-Cathrin Koschker, Martin Fassnacht, et al.
Breast Cancer Research and Treatment|November 8, 2012
The clinical consequences of hemizygosity across 2 MB of 10q23 are restricted to Cowden syndromeCheryl M Lewis, Dawei Bu, Venetia Sarode, et al.
Human Molecular Genetics|January 29, 2014
Germline disruption of Pten localization causes enhanced sex-dependent social motivation and increased glial productionAmanda K Tilot, Mary K Gaugler, Qi Yu, et al.
Pageof 56