Lista de obras - Giampaolo Trivellin - Dominio Público Uruguay

A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers.

artículo científico publicado en 2016

A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype.

artículo científico publicado en 2013

AIP and its interacting partners.

artículo científico publicado en 2011

Adrenal lesions in acromegaly: do metabolic aspects and aryl hydrocarbon receptor interacting protein gene have a role? Evaluation at baseline and after long-term follow-up

artículo científico publicado en 2010

Aggressive tumor growth and clinical evolution in a patient with X-linked acro-gigantism syndrome

artículo científico publicado en 2015

An orphan G-protein-coupled receptor causes human gigantism and/or acromegaly: Molecular biology and clinical correlations

artículo científico publicado en 2018

CD40LG duplications in patients with X-LAG syndrome commonly undergo random X-chromosome inactivation

scientific article published on 15 February 2019

Chaperones, somatotroph tumors and the cyclic AMP (cAMP)-dependent protein kinase (PKA) pathway

scientific article published on 03 October 2019

Characterization of GPR101 transcript structure and expression patterns

artículo científico publicado en 2016

Characterization of SNARE proteins in human pituitary adenomas: targeted secretion inhibitors as a new strategy for the treatment of acromegaly?

artículo científico publicado en 2013

Characterization of aryl hydrocarbon receptor interacting protein (AIP) mutations in familial isolated pituitary adenoma families

artículo científico publicado en 2010

Characterization of the adiponectin promoter + Cre recombinase insertion in the Tg(Adipoq-cre)1Evdr mouse by targeted locus amplification and droplet digital PCR

artículo científico publicado en 2021

Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients.

artículo científico publicado en 2015

Cyclic 3',5'-adenosine monophosphate (cAMP) signaling in the anterior pituitary gland in health and disease

artículo científico publicado en 2017

Familial isolated pituitary adenomas: An emerging clinical entity ⬇️

artículo científico publicado el 1 de diciembre de 2012

GHRH excess and blockade in X-LAG syndrome.

artículo científico publicado en 2015

GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency

artículo científico publicado en 2016

Genetics of gigantism and acromegaly

artículo científico publicado en 2016

Genetics of pituitary adenomas.

artículo científico publicado en 2013

Genetics, clinical features and outcomes of non-syndromic pituitary gigantism: experience of a single center from Sao Paulo, Brazil

artículo científico publicado en 2020

Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study

artículo científico publicado en 2016

Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation

artículo científico publicado en 2014

Gigantism, acromegaly, and GPR101 mutations

artículo científico publicado en 2015

Increased Population Risk of AIP-Related Acromegaly and Gigantism in Ireland

artículo científico publicado en 2016

Interaction of AIP with protein kinase A (cAMP-dependent protein kinase).

artículo científico publicado en 2018

Is IGSF1 involved in human pituitary tumor formation?

artículo científico publicado en 2014

Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers.

artículo científico publicado en 2015

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease

artículo científico publicado en 2017

MEN1, MEN4, and Carney Complex: Pathology and Molecular Genetics

artículo científico publicado en 2016

Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation

artículo científico publicado en 2014

MicroRNA miR-107 is overexpressed in pituitary adenomas and inhibits the expression of aryl hydrocarbon receptor-interacting protein in vitro

artículo científico publicado en 2012

MicroRNAs: Suggested role in pituitary adenoma pathogenesis

artículo científico publicado en 2013

Oncogene-induced senescence in pituitary adenomas and carcinomas.

artículo científico publicado en 2012

Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia

artículo científico publicado en 2010

Rapid Proteasomal Degradation of Mutant Proteins Is the Primary Mechanism Leading to Tumorigenesis in Patients With Missense AIP Mutations.

artículo científico publicado en 2016

Regulation of aryl hydrocarbon receptor interacting protein (AIP) protein expression by MiR-34a in sporadic somatotropinomas

artículo científico publicado en 2015

Screening for GPR101 defects in pediatric pituitary corticotropinomas

artículo científico publicado en 2016

Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects

artículo científico publicado en 2016

Somatostatin analogs modulate AIP in somatotroph adenomas: the role of the ZAC1 pathway.

artículo científico publicado en 2012

Structure of the TPR Domain of AIP: Lack of Client Protein Interaction with the C-Terminal α-7 Helix of the TPR Domain of AIP Is Sufficient for Pituitary Adenoma Predisposition

artículo científico publicado en 2012

The Glucose-Dependent Insulinotropic Polypeptide Receptor is Overexpressed Amongst GNAS1 Mutation-Negative Somatotropinomas and Drives Growth Hormone (GH)-Promoter Activity in GH3 Cells ⬇️

artículo científico publicado el 1 de julio de 2011

The R304X mutation of the aryl hydrocarbon receptor interacting protein gene in familial isolated pituitary adenomas: Mutational hot-spot or founder effect?

artículo científico publicado en 2010

X-linked acrogigantism syndrome: clinical profile and therapeutic responses

artículo científico publicado en 2015

Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle Tone Refines the X-Linked Acrogigantism Genetic Locus

artículo científico publicado en 2018

cAMP-specific PDE4 phosphodiesterases and AIP in the pathogenesis of pituitary tumors.

artículo científico publicado en 2016

Lista de obras de Giampaolo Trivellin

A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers.

A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype.

AIP and its interacting partners.

Adrenal lesions in acromegaly: do metabolic aspects and aryl hydrocarbon receptor interacting protein gene have a role? Evaluation at baseline and after long-term follow-up

Aggressive tumor growth and clinical evolution in a patient with X-linked acro-gigantism syndrome

An orphan G-protein-coupled receptor causes human gigantism and/or acromegaly: Molecular biology and clinical correlations

CD40LG duplications in patients with X-LAG syndrome commonly undergo random X-chromosome inactivation

Chaperones, somatotroph tumors and the cyclic AMP (cAMP)-dependent protein kinase (PKA) pathway

Characterization of GPR101 transcript structure and expression patterns

Characterization of SNARE proteins in human pituitary adenomas: targeted secretion inhibitors as a new strategy for the treatment of acromegaly?

Characterization of aryl hydrocarbon receptor interacting protein (AIP) mutations in familial isolated pituitary adenoma families

Characterization of the adiponectin promoter + Cre recombinase insertion in the Tg(Adipoq-cre)1Evdr mouse by targeted locus amplification and droplet digital PCR

Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients.

Cyclic 3',5'-adenosine monophosphate (cAMP) signaling in the anterior pituitary gland in health and disease

Familial isolated pituitary adenomas: An emerging clinical entity ⬇️

GHRH excess and blockade in X-LAG syndrome.

GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency

Genetics of gigantism and acromegaly

Genetics of pituitary adenomas.

Genetics, clinical features and outcomes of non-syndromic pituitary gigantism: experience of a single center from Sao Paulo, Brazil

Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study

Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation

Gigantism, acromegaly, and GPR101 mutations

Increased Population Risk of AIP-Related Acromegaly and Gigantism in Ireland

Interaction of AIP with protein kinase A (cAMP-dependent protein kinase).

Is IGSF1 involved in human pituitary tumor formation?

Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers.

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease

MEN1, MEN4, and Carney Complex: Pathology and Molecular Genetics

Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation

MicroRNA miR-107 is overexpressed in pituitary adenomas and inhibits the expression of aryl hydrocarbon receptor-interacting protein in vitro

MicroRNAs: Suggested role in pituitary adenoma pathogenesis

Oncogene-induced senescence in pituitary adenomas and carcinomas.

Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia

Rapid Proteasomal Degradation of Mutant Proteins Is the Primary Mechanism Leading to Tumorigenesis in Patients With Missense AIP Mutations.

Regulation of aryl hydrocarbon receptor interacting protein (AIP) protein expression by MiR-34a in sporadic somatotropinomas

Screening for GPR101 defects in pediatric pituitary corticotropinomas

Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects

Somatostatin analogs modulate AIP in somatotroph adenomas: the role of the ZAC1 pathway.

Structure of the TPR Domain of AIP: Lack of Client Protein Interaction with the C-Terminal α-7 Helix of the TPR Domain of AIP Is Sufficient for Pituitary Adenoma Predisposition

The Glucose-Dependent Insulinotropic Polypeptide Receptor is Overexpressed Amongst GNAS1 Mutation-Negative Somatotropinomas and Drives Growth Hormone (GH)-Promoter Activity in GH3 Cells ⬇️

The R304X mutation of the aryl hydrocarbon receptor interacting protein gene in familial isolated pituitary adenomas: Mutational hot-spot or founder effect?

X-linked acrogigantism syndrome: clinical profile and therapeutic responses

Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle Tone Refines the X-Linked Acrogigantism Genetic Locus

cAMP-specific PDE4 phosphodiesterases and AIP in the pathogenesis of pituitary tumors.