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Emilia Modolo Pinto

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

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Cancer|September 3, 2020
What 20 years of research has taught us about the TP53 p.R337H mutationEmilia Modolo Pinto, Gerard P Zambetti
Current Opinion in Endocrine and Metabolic Research|June 19, 2020
Contemporary preclinical human models of adrenocortical carcinomaEmilia Modolo Pinto, Katja Kiseljak-Vassiliades, Constanze Hantel
Best Practice & Research. Clinical Endocrinology & Metabolism|July 9, 2020
Pediatric adrenocortical tumoursEmilia Modolo Pinto, Gerard P Zambetti, Carlos Rodriguez-Galindo
Frontiers in Endocrinology|November 22, 2021
Adrenocortical Tumors in Children With Constitutive Chromosome 11p15 Paternal Uniparental Disomy: Implications for Diagnosis and TreatmentEmilia Modolo Pinto, Carlos Rodriguez-Galindo, Catherine G Lam, et al.
Cold Spring Harbor Molecular Case Studies|December 5, 2023
Clinical and functional analysis of the germline <i>TP53</i> p.K164E acetylation site variantEmilia Modolo Pinto, Enilze M S F Ribeiro, Jinling Wang, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 29, 2025
Reconstructing the Origin and Demographic Expansion of the TP53 p.R337H Founder Variant in BrazilEmilia Modolo Pinto, Joao Carlos Degraf Muzzi, José Andres Yunes, et al.
Clinical Endocrinology|September 27, 2003
Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocious pubertyAna Claudia Latronico, Ana Elisa C Billerbeck, Emilia Modolo Pinto, et al.
Pituitary|August 6, 2009
Possible role of a radiation-induced p53 mutation in a Nelson's syndrome patient with a fatal outcomeEmilia Modolo Pinto, Sheila A C Siqueira, Priscilla Cukier, et al.
The Journal of Clinical Endocrinology and Metabolism|March 16, 2007
Evaluating the roles of follicle-stimulating hormone receptor polymorphisms in gonadal hyperstimulation associated with severe juvenile primary hypothyroidismGinny L Ryan, Xiuyan Feng, Catarina Brasil d'Alva, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
[Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with Carney complex caused by the novel nonsense mutation p.Y21X]Madson Q Almeida, Luciana Pinto Brito, Sorahia Domenice, et al.
Pageof 2

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

Sort By:
Pageof 2
Cancer|September 3, 2020
What 20 years of research has taught us about the TP53 p.R337H mutationEmilia Modolo Pinto, Gerard P Zambetti
Current Opinion in Endocrine and Metabolic Research|June 19, 2020
Contemporary preclinical human models of adrenocortical carcinomaEmilia Modolo Pinto, Katja Kiseljak-Vassiliades, Constanze Hantel
Best Practice & Research. Clinical Endocrinology & Metabolism|July 9, 2020
Pediatric adrenocortical tumoursEmilia Modolo Pinto, Gerard P Zambetti, Carlos Rodriguez-Galindo
Frontiers in Endocrinology|November 22, 2021
Adrenocortical Tumors in Children With Constitutive Chromosome 11p15 Paternal Uniparental Disomy: Implications for Diagnosis and TreatmentEmilia Modolo Pinto, Carlos Rodriguez-Galindo, Catherine G Lam, et al.
Cold Spring Harbor Molecular Case Studies|December 5, 2023
Clinical and functional analysis of the germline <i>TP53</i> p.K164E acetylation site variantEmilia Modolo Pinto, Enilze M S F Ribeiro, Jinling Wang, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 29, 2025
Reconstructing the Origin and Demographic Expansion of the TP53 p.R337H Founder Variant in BrazilEmilia Modolo Pinto, Joao Carlos Degraf Muzzi, José Andres Yunes, et al.
Clinical Endocrinology|September 27, 2003
Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocious pubertyAna Claudia Latronico, Ana Elisa C Billerbeck, Emilia Modolo Pinto, et al.
Pituitary|August 6, 2009
Possible role of a radiation-induced p53 mutation in a Nelson's syndrome patient with a fatal outcomeEmilia Modolo Pinto, Sheila A C Siqueira, Priscilla Cukier, et al.
The Journal of Clinical Endocrinology and Metabolism|March 16, 2007
Evaluating the roles of follicle-stimulating hormone receptor polymorphisms in gonadal hyperstimulation associated with severe juvenile primary hypothyroidismGinny L Ryan, Xiuyan Feng, Catarina Brasil d'Alva, et al.
Arquivos Brasileiros De Endocrinologia E Metabologia|January 27, 2009
[Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with Carney complex caused by the novel nonsense mutation p.Y21X]Madson Q Almeida, Luciana Pinto Brito, Sorahia Domenice, et al.
Pageof 2