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Charis Eng

Showing results (401-410 of 555) with videos related to

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Clinical and Translational Gastroenterology|December 15, 2012
Upper and Lower Gastrointestinal Findings in PTEN Mutation-Positive Cowden Syndrome Patients Participating in an Active Surveillance ProgramZohar Levi, Hagit N Baris, Inbal Kedar, et al.
American Journal of Medical Genetics. Part A|May 26, 2012
PTEN hamartoma tumor syndrome and Gorham-Stout phenomenonSaskia M J Hopman, Rick R Van Rijn, Charis Eng, et al.
Endocrine-Related Cancer|December 25, 2015
Germline PARP4 mutations in patients with primary thyroid and breast cancersYuji Ikeda, Kazuma Kiyotani, Poh Yin Yew, et al.
The American Journal of Surgical Pathology|December 7, 2005
Functioning paraganglioma and gastrointestinal stromal tumor of the jejunum in three women: syndrome or coincidenceColin G Perry, William F Young, Sarah R McWhinney, et al.
Gastroenterology|July 1, 2015
Exome Sequencing Reveals Germline SMAD9 Mutation That Reduces Phosphatase and Tensin Homolog Expression and Is Associated With Hamartomatous Polyposis and Gastrointestinal GanglioneuromasJoanne Ngeow, Wanfeng Yu, Lamis Yehia, et al.
Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 4, 2007
Pilot study of rosiglitazone therapy in women with breast cancer: effects of short-term therapy on tumor tissue and serum markersLisa D Yee, Nita Williams, Ping Wen, et al.
NPJ Genomic Medicine|December 22, 2017
Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practicesBrandie Heald, Lisa Rybicki, Diane Clements, et al.
Surgery|April 26, 2008
Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutationsMarta S Sarquis, Leticia G Silveira, Flavio J Pimenta, et al.
Biorxiv : the Preprint Server for Biology|May 10, 2023
Structurally-informed human interactome reveals proteome-wide perturbations by disease mutationsDapeng Xiong, Yunguang Qiu, Junfei Zhao, et al.
Pageof 56

Showing results (401-410 of 555) with videos related to

Sort By:
Pageof 56
Clinical and Translational Gastroenterology|December 15, 2012
Upper and Lower Gastrointestinal Findings in PTEN Mutation-Positive Cowden Syndrome Patients Participating in an Active Surveillance ProgramZohar Levi, Hagit N Baris, Inbal Kedar, et al.
American Journal of Medical Genetics. Part A|May 26, 2012
PTEN hamartoma tumor syndrome and Gorham-Stout phenomenonSaskia M J Hopman, Rick R Van Rijn, Charis Eng, et al.
Endocrine-Related Cancer|December 25, 2015
Germline PARP4 mutations in patients with primary thyroid and breast cancersYuji Ikeda, Kazuma Kiyotani, Poh Yin Yew, et al.
The American Journal of Surgical Pathology|December 7, 2005
Functioning paraganglioma and gastrointestinal stromal tumor of the jejunum in three women: syndrome or coincidenceColin G Perry, William F Young, Sarah R McWhinney, et al.
Gastroenterology|July 1, 2015
Exome Sequencing Reveals Germline SMAD9 Mutation That Reduces Phosphatase and Tensin Homolog Expression and Is Associated With Hamartomatous Polyposis and Gastrointestinal GanglioneuromasJoanne Ngeow, Wanfeng Yu, Lamis Yehia, et al.
Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 4, 2007
Pilot study of rosiglitazone therapy in women with breast cancer: effects of short-term therapy on tumor tissue and serum markersLisa D Yee, Nita Williams, Ping Wen, et al.
NPJ Genomic Medicine|December 22, 2017
Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practicesBrandie Heald, Lisa Rybicki, Diane Clements, et al.
Surgery|April 26, 2008
Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutationsMarta S Sarquis, Leticia G Silveira, Flavio J Pimenta, et al.
Biorxiv : the Preprint Server for Biology|May 10, 2023
Structurally-informed human interactome reveals proteome-wide perturbations by disease mutationsDapeng Xiong, Yunguang Qiu, Junfei Zhao, et al.
Pageof 56