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Showing results (281-290 of 293) with videos related to

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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 5, 2025
Hyalinizing Clear Cell Carcinoma of the Head and Neck: A Multicenter Retrospective Study of 87 Cases Focusing on Prognostic Pathologic Features and Grading SchemeBin Xu, Kartik Viswanathan, Marie Barbesier, et al.
American Journal of Preventive Medicine|May 13, 2023
Vaping and Hookah Use Among Medical Trainees: A Multinational Survey StudyLuiza Helena Degani-Costa, Fernando P Bruno, Fernanda Gushken, et al.
Human Molecular Genetics|January 11, 2015
Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencingJohn W Kunstman, C Christofer Juhlin, Gerald Goh, et al.
Nature Genetics|April 22, 2014
Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumorsGerald Goh, Ute I Scholl, James M Healy, et al.
Plos One|October 3, 2012
Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palateAriadne Letra, Walid Fakhouri, Renata F Fonseca, et al.
Clinical Endocrinology|August 8, 2015
Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotypeUte I Scholl, James M Healy, Anne Thiel, et al.
Genes, Chromosomes & Cancer|June 3, 2015
Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated geneC Christofer Juhlin, Adam Stenman, Felix Haglund, et al.
Elife|April 25, 2015
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronismUte I Scholl, Gabriel Stölting, Carol Nelson-Williams, et al.
The Journal of Clinical Endocrinology and Metabolism|December 10, 2014
Whole-exome sequencing characterizes the landscape of somatic mutations and copy number alterations in adrenocortical carcinomaC Christofer Juhlin, Gerald Goh, James M Healy, et al.
Nature Genetics|August 6, 2013
Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronismUte I Scholl, Gerald Goh, Gabriel Stölting, et al.
Pageof 30

Showing results (281-290 of 293) with videos related to

Sort By:
Pageof 30
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 5, 2025
Hyalinizing Clear Cell Carcinoma of the Head and Neck: A Multicenter Retrospective Study of 87 Cases Focusing on Prognostic Pathologic Features and Grading SchemeBin Xu, Kartik Viswanathan, Marie Barbesier, et al.
American Journal of Preventive Medicine|May 13, 2023
Vaping and Hookah Use Among Medical Trainees: A Multinational Survey StudyLuiza Helena Degani-Costa, Fernando P Bruno, Fernanda Gushken, et al.
Human Molecular Genetics|January 11, 2015
Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencingJohn W Kunstman, C Christofer Juhlin, Gerald Goh, et al.
Nature Genetics|April 22, 2014
Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumorsGerald Goh, Ute I Scholl, James M Healy, et al.
Plos One|October 3, 2012
Interaction between IRF6 and TGFA genes contribute to the risk of nonsyndromic cleft lip/palateAriadne Letra, Walid Fakhouri, Renata F Fonseca, et al.
Clinical Endocrinology|August 8, 2015
Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotypeUte I Scholl, James M Healy, Anne Thiel, et al.
Genes, Chromosomes & Cancer|June 3, 2015
Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated geneC Christofer Juhlin, Adam Stenman, Felix Haglund, et al.
Elife|April 25, 2015
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronismUte I Scholl, Gabriel Stölting, Carol Nelson-Williams, et al.
The Journal of Clinical Endocrinology and Metabolism|December 10, 2014
Whole-exome sequencing characterizes the landscape of somatic mutations and copy number alterations in adrenocortical carcinomaC Christofer Juhlin, Gerald Goh, James M Healy, et al.
Nature Genetics|August 6, 2013
Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronismUte I Scholl, Gerald Goh, Gabriel Stölting, et al.
Pageof 30