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Ebtesam Qasem

Showing results (1-10 of 17) with videos related to

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Thyroid : Official Journal of the American Thyroid Association|February 25, 2016
HABP2 Gene Mutations Do Not Cause Familial or Sporadic Non-Medullary Thyroid Cancer in a Highly Inbred Middle Eastern PopulationAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Oncotarget|July 11, 2019
GPCR-mediated PI3K pathway mutations in pediatric and adult thyroid cancerAvaniyapuram Kannan Murugan, Ebtesam Qasem, Hindi Al-Hindi, et al.
Molecular and Clinical Oncology|August 31, 2021
Analysis of <i>ALK, IDH1, IDH2</i> and <i>MMP8</i> somatic mutations in differentiated thyroid cancersAvaniyapuram Kannan Murugan, Ebtesam Qasem, Hindi Al-Hindi, et al.
Journal of Translational Medicine|July 9, 2016
Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancerAvaniyapuram Kannan Murugan, Ebtesam Qasem, Hindi Al-Hindi, et al.
Thyroid : Official Journal of the American Thyroid Association|November 9, 2016
Single Point Mutations in Pediatric Differentiated Thyroid CancerAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|June 18, 2014
Apparent Mineralocorticoid Excess Caused by a Novel Mutation in 11-β Hydroxysteroid Dehydrogenase Type 2 Enzyme: Its Genetics and Response to TherapyAli S Alzahrani, Nasser Aljuhani, Ebtesam Qasem, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|August 8, 2014
Divergent gender identity in three siblings with 46XX karyotype and severely virilizing congenital adrenal hyperplasia caused by a novel CYP11B1 mutationBassam Bin-Abbas, Doha Al-Humaida, Afaf Al-Sagheir, et al.
Endocrine-Related Cancer|September 11, 2015
TERT promoter mutations in thyroid cancer: a report from a Middle Eastern populationEbtesam Qasem, Avaniyapuram Kannan Murugan, Hindi Al-Hindi, et al.
Endocrine|June 27, 2019
Correction to: Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancerAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Endocrine|October 1, 2018
Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancerAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Thyroid : Official Journal of the American Thyroid Association|February 25, 2016
HABP2 Gene Mutations Do Not Cause Familial or Sporadic Non-Medullary Thyroid Cancer in a Highly Inbred Middle Eastern PopulationAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Oncotarget|July 11, 2019
GPCR-mediated PI3K pathway mutations in pediatric and adult thyroid cancerAvaniyapuram Kannan Murugan, Ebtesam Qasem, Hindi Al-Hindi, et al.
Molecular and Clinical Oncology|August 31, 2021
Analysis of <i>ALK, IDH1, IDH2</i> and <i>MMP8</i> somatic mutations in differentiated thyroid cancersAvaniyapuram Kannan Murugan, Ebtesam Qasem, Hindi Al-Hindi, et al.
Journal of Translational Medicine|July 9, 2016
Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancerAvaniyapuram Kannan Murugan, Ebtesam Qasem, Hindi Al-Hindi, et al.
Thyroid : Official Journal of the American Thyroid Association|November 9, 2016
Single Point Mutations in Pediatric Differentiated Thyroid CancerAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|June 18, 2014
Apparent Mineralocorticoid Excess Caused by a Novel Mutation in 11-β Hydroxysteroid Dehydrogenase Type 2 Enzyme: Its Genetics and Response to TherapyAli S Alzahrani, Nasser Aljuhani, Ebtesam Qasem, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|August 8, 2014
Divergent gender identity in three siblings with 46XX karyotype and severely virilizing congenital adrenal hyperplasia caused by a novel CYP11B1 mutationBassam Bin-Abbas, Doha Al-Humaida, Afaf Al-Sagheir, et al.
Endocrine-Related Cancer|September 11, 2015
TERT promoter mutations in thyroid cancer: a report from a Middle Eastern populationEbtesam Qasem, Avaniyapuram Kannan Murugan, Hindi Al-Hindi, et al.
Endocrine|June 27, 2019
Correction to: Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancerAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Endocrine|October 1, 2018
Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancerAli S Alzahrani, Avaniyapuram Kannan Murugan, Ebtesam Qasem, et al.
Pageof 2