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Charis Eng

Showing results (201-210 of 555) with videos related to

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Chest|April 12, 2007
Long-term outcome in a patient with pulmonary hypertension and hereditary hemorrhagic telangiectasiaOmar A Minai, Christina Rigelsky, Charis Eng, et al.
The Journal of Clinical Endocrinology and Metabolism|September 30, 2011
Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterationsJoanne Ngeow, Jessica Mester, Lisa A Rybicki, et al.
Human Molecular Genetics|March 1, 2013
Germline and somatic KLLN alterations in breast cancer dysregulate G2 arrestEmily A Nizialek, Charissa Peterson, Jessica L Mester, et al.
Human Molecular Genetics|December 16, 2020
Germline EGFR variants are over-represented in adolescents and young adults (AYA) with adrenocortical carcinomaSara Akhavanfard, Lamis Yehia, Roshan Padmanabhan, et al.
The Journal of Clinical Endocrinology and Metabolism|April 10, 2014
Germline alterations in RASAL1 in Cowden syndrome patients presenting with follicular thyroid cancer and in individuals with apparently sporadic epithelial thyroid cancerJoanne Ngeow, Ying Ni, Rita Tohme, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 30, 2014
Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutationsJoanne Ngeow, Kim Stanuch, Jessica L Mester, et al.
American Journal of Human Genetics|March 22, 2008
SNP arrays in heterogeneous tissue: highly accurate collection of both germline and somatic genetic information from unpaired single tumor samplesGuillaume Assié, Thomas LaFramboise, Petra Platzer, et al.
Oncogene|July 26, 2003
Frequent epigenetic inactivation of the SLIT2 gene in gliomasAshraf Dallol, Dietmar Krex, Luke Hesson, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephalyJudith A Hobert, Rebecca Embacher, Jessica L Mester, et al.
The Lancet. Diabetes & Endocrinology|November 29, 2020
Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literatureIrina Bancos, Elizabeth Atkinson, Charis Eng, et al.
Pageof 56

Showing results (201-210 of 555) with videos related to

Sort By:
Pageof 56
Chest|April 12, 2007
Long-term outcome in a patient with pulmonary hypertension and hereditary hemorrhagic telangiectasiaOmar A Minai, Christina Rigelsky, Charis Eng, et al.
The Journal of Clinical Endocrinology and Metabolism|September 30, 2011
Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterationsJoanne Ngeow, Jessica Mester, Lisa A Rybicki, et al.
Human Molecular Genetics|March 1, 2013
Germline and somatic KLLN alterations in breast cancer dysregulate G2 arrestEmily A Nizialek, Charissa Peterson, Jessica L Mester, et al.
Human Molecular Genetics|December 16, 2020
Germline EGFR variants are over-represented in adolescents and young adults (AYA) with adrenocortical carcinomaSara Akhavanfard, Lamis Yehia, Roshan Padmanabhan, et al.
The Journal of Clinical Endocrinology and Metabolism|April 10, 2014
Germline alterations in RASAL1 in Cowden syndrome patients presenting with follicular thyroid cancer and in individuals with apparently sporadic epithelial thyroid cancerJoanne Ngeow, Ying Ni, Rita Tohme, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 30, 2014
Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutationsJoanne Ngeow, Kim Stanuch, Jessica L Mester, et al.
American Journal of Human Genetics|March 22, 2008
SNP arrays in heterogeneous tissue: highly accurate collection of both germline and somatic genetic information from unpaired single tumor samplesGuillaume Assié, Thomas LaFramboise, Petra Platzer, et al.
Oncogene|July 26, 2003
Frequent epigenetic inactivation of the SLIT2 gene in gliomasAshraf Dallol, Dietmar Krex, Luke Hesson, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephalyJudith A Hobert, Rebecca Embacher, Jessica L Mester, et al.
The Lancet. Diabetes & Endocrinology|November 29, 2020
Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literatureIrina Bancos, Elizabeth Atkinson, Charis Eng, et al.
Pageof 56