Lista de obras - Sunita K Agarwal - Dominio Público Uruguay

A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13.

artículo científico publicado en 1997

A patient with MEN1 typical features and MEN2-like features

artículo científico publicado en 2016

An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and protein

artículo científico publicado en 2009

Characterization of a MEN1 ortholog from Drosophila melanogaster

artículo científico publicado en 2001

Chronic administration of growth hormone (GH) to adult chickens exerts marked effects on circulating concentrations of insulin-like growth factor-I (IGF-I), IGF binding proteins, hepatic GH regulated gene I, and hepatic GH receptor mRNA

artículo científico publicado en 1997

Cloning and expression of a novel chicken sulfotransferase cDNA regulated by GH.

artículo científico publicado en 1999

Common ancestral mutations in theMEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland ⬇️

artículo científico publicado el 1 de enero de 1998

Comparative genomic hybridization analysis of human parathyroid tumors

artículo científico publicado en 1998

Comparison of gene expression in normal and growth hormone receptor-deficient dwarf chickens reveals a novel growth hormone regulated gene

artículo científico publicado en 1995

Consequence of Menin Deficiency in Mouse Adipocytes Derived by In Vitro Differentiation

artículo científico publicado en 2015

Distribution of menin-occupied regions in chromatin specifies a broad role of menin in transcriptional regulation

artículo científico publicado en 2007

Dysfunctional growth hormone receptor in a strain of sex-linked dwarf chicken: evidence for a mutation in the intracellular domain

artículo científico publicado en 1994

Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region

artículo científico publicado en 1997

Epigenetic regulation in the tumorigenesis of MEN1-associated endocrine cell types

artículo científico publicado en 2018

Epigenetic regulation of the lncRNA MEG3 and its target c-MET in pancreatic neuroendocrine tumors

artículo científico publicado en 2015

Ethnicity of Patients With Germline GCM2-Activating Variants and Primary Hyperparathyroidism.

artículo científico publicado en 2017

Exploring the tumors of multiple endocrine neoplasia type 1 in mouse models for basic and preclinical studies

artículo científico publicado en 2014

FBP1 Is an Interacting Partner of Menin.

artículo científico publicado en 2014

Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.

artículo científico publicado en 2004

Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds

artículo científico publicado en 2002

Familial isolated primary hyperparathyroidism associated with germline GCM2 mutations is more aggressive and has a lesser rate of biochemical cure

artículo científico publicado en 2017

Frequency and consequence of the recurrent YY1 p.T372R mutation in sporadic insulinomas

artículo científico publicado en 2018

Functional Defects From Endocrine Disease-Associated Mutations in HLXB9 and Its Interacting Partner, NONO.

artículo científico publicado en 2018

GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism

artículo científico publicado en 2016

GSK-3β protein phosphorylates and stabilizes HLXB9 protein in insulinoma cells to form a targetable mechanism of controlling insulinoma cell proliferation

scientific article published on 14 January 2014

Genetic interactions between Drosophila melanogaster menin and Jun/Fos

artículo científico publicado en 2006

Genome-wide analysis of menin binding provides insights into MEN1 tumorigenesis

artículo científico publicado en 2006

Genome-wide characterization of menin-dependent H3K4me3 reveals a specific role for menin in the regulation of genes implicated in MEN1-like tumors

artículo científico publicado en 2012

Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer

artículo científico publicado en 2015

Germline and somatic mutations in cyclin-dependent kinase inhibitor genes CDKN1A, CDKN2B, and CDKN2C in sporadic parathyroid adenomas.

artículo científico publicado en 2013

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states

scientific article published on 01 July 1997

Identification and characterization of JunD missense mutants that lack menin binding

artículo científico publicado en 2000

Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung ⬇️

artículo científico publicado el 1 de diciembre de 1997

Interferon activity of mitogen-induced chicken splenic lymphocytes which do not express interferon mRNA.

artículo científico publicado en 1996

Isolation, characterization, expression and functional analysis of the zebrafish ortholog of MEN1.

artículo científico publicado en 2000

MEN1 gene analysis in sporadic adrenocortical neoplasms.

artículo científico publicado en 1999

Menin immunoreactivity in secretory granules of human pancreatic islet cells

artículo científico publicado en 2014

Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription

artículo científico publicado en 1999

Menin molecular interactions: insights into normal functions and tumorigenesis.

artículo científico publicado en 2005

Menin, a tumor suppressor, associates with nonmuscle myosin II-A heavy chain

artículo científico publicado en 2003

Metformin targets Mitochondrial Glycerophosphate Dehydrogenase (mGPDH) to control Rate of Oxidative Phosphorylation and growth of thyroid cancer in vitro and in vivo.

artículo científico publicado en 2018

Mouse embryo fibroblasts lacking the tumor suppressor menin show altered expression of extracellular matrix protein genes.

artículo científico publicado en 2007

Multiple Endocrine Neoplasia Type 1: Latest Insights

artículo científico publicado en 2020

Multiple endocrine neoplasia type 1

artículo científico publicado en 2013

Multiple endocrine neoplasia type 1 variant with frequent prolactinoma and rare gastrinoma

artículo científico publicado en 2004

Multiple endocrine neoplasia type 1: new clinical and basic findings

artículo científico publicado en 2001

Overexpression of a truncated growth hormone receptor in the sex-linked dwarf chicken: evidence for a splice mutation.

artículo científico publicado en 1993

Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression

artículo científico publicado en 2005

Parathyroid tumor development involves deregulation of homeobox genes

artículo científico publicado en 2008

Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1.

artículo científico publicado en 2000

Pro-oncogenic Roles of HLXB9 Protein in Insulinoma Cells through Interaction with Nono Protein and Down-regulation of the c-Met Inhibitor Cblb (Casitas B-lineage Lymphoma b).

artículo científico publicado en 2015

Probability of Positive Genetic Testing Results in Patients with Family History of Primary Hyperparathyroidism

artículo científico publicado en 2018

Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states

artículo científico publicado en 2009

Reoperative Surgery in Patients with Multiple Endocrine Neoplasia Type 1 Associated Primary Hyperparathyroidism.

artículo científico publicado en 2016

Somatic mutation of the MEN1 gene in parathyroid tumours

artículo científico publicado en 1997

Study of the multiple endocrine neoplasia type 1, growth hormone-releasing hormone receptor, Gs alpha, and Gi2 alpha genes in isolated familial acromegaly

artículo científico publicado en 2001

The 32-kilodalton subunit of replication protein A interacts with menin, the product of the MEN1 tumor suppressor gene

artículo científico publicado en 2003

The Long Non-Coding RNA MEG3 is an Epigenetic Determinant of Oncogenic Signaling in Functional Pancreatic Neuroendocrine Tumor Cells

artículo científico publicado en 2017

The MEN1 gene and pituitary tumours.

artículo científico publicado en 2009

The adenine phosphoribosyltransferase-encoding gene of Arabidopsis thaliana.

artículo científico publicado en 1994

The embryonic transcription factor Hlxb9 is a menin interacting partner that controls pancreatic β-cell proliferation and the expression of insulin regulators

artículo científico publicado en 2013

The future: genetics advances in MEN1 therapeutic approaches and management strategies.

artículo científico publicado en 2017

The gene for multiple endocrine neoplasia type 1: recent findings.

artículo científico publicado en 1999

The parafibromin tumor suppressor protein interacts with actin-binding proteins actinin-2 and actinin-3.

artículo científico publicado en 2008

The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations

artículo científico publicado en 2007

The tumor suppressor protein menin inhibits AKT activation by regulating its cellular localization.

artículo científico publicado en 2010

Transcription factor JunD, deprived of menin, switches from growth suppressor to growth promoter

artículo científico publicado en 2003

Transcriptional alterations in hereditary and sporadic nonfunctioning pancreatic neuroendocrine tumors according to genotype.

artículo científico publicado en 2017

Lista de obras de Sunita K Agarwal

A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13.

A patient with MEN1 typical features and MEN2-like features

An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and protein

Characterization of a MEN1 ortholog from Drosophila melanogaster

Chronic administration of growth hormone (GH) to adult chickens exerts marked effects on circulating concentrations of insulin-like growth factor-I (IGF-I), IGF binding proteins, hepatic GH regulated gene I, and hepatic GH receptor mRNA

Cloning and expression of a novel chicken sulfotransferase cDNA regulated by GH.

Common ancestral mutations in theMEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland ⬇️

Comparative genomic hybridization analysis of human parathyroid tumors

Comparison of gene expression in normal and growth hormone receptor-deficient dwarf chickens reveals a novel growth hormone regulated gene

Consequence of Menin Deficiency in Mouse Adipocytes Derived by In Vitro Differentiation

Distribution of menin-occupied regions in chromatin specifies a broad role of menin in transcriptional regulation

Dysfunctional growth hormone receptor in a strain of sex-linked dwarf chicken: evidence for a mutation in the intracellular domain

Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region

Epigenetic regulation in the tumorigenesis of MEN1-associated endocrine cell types

Epigenetic regulation of the lncRNA MEG3 and its target c-MET in pancreatic neuroendocrine tumors

Ethnicity of Patients With Germline GCM2-Activating Variants and Primary Hyperparathyroidism.

Exploring the tumors of multiple endocrine neoplasia type 1 in mouse models for basic and preclinical studies

FBP1 Is an Interacting Partner of Menin.

Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.

Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds

Familial isolated primary hyperparathyroidism associated with germline GCM2 mutations is more aggressive and has a lesser rate of biochemical cure

Frequency and consequence of the recurrent YY1 p.T372R mutation in sporadic insulinomas

Functional Defects From Endocrine Disease-Associated Mutations in HLXB9 and Its Interacting Partner, NONO.

GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism

GSK-3β protein phosphorylates and stabilizes HLXB9 protein in insulinoma cells to form a targetable mechanism of controlling insulinoma cell proliferation

Genetic interactions between Drosophila melanogaster menin and Jun/Fos

Genome-wide analysis of menin binding provides insights into MEN1 tumorigenesis

Genome-wide characterization of menin-dependent H3K4me3 reveals a specific role for menin in the regulation of genes implicated in MEN1-like tumors

Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer

Germline and somatic mutations in cyclin-dependent kinase inhibitor genes CDKN1A, CDKN2B, and CDKN2C in sporadic parathyroid adenomas.

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states

Identification and characterization of JunD missense mutants that lack menin binding

Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung ⬇️

Interferon activity of mitogen-induced chicken splenic lymphocytes which do not express interferon mRNA.

Isolation, characterization, expression and functional analysis of the zebrafish ortholog of MEN1.

MEN1 gene analysis in sporadic adrenocortical neoplasms.

Menin immunoreactivity in secretory granules of human pancreatic islet cells

Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription

Menin molecular interactions: insights into normal functions and tumorigenesis.

Menin, a tumor suppressor, associates with nonmuscle myosin II-A heavy chain

Metformin targets Mitochondrial Glycerophosphate Dehydrogenase (mGPDH) to control Rate of Oxidative Phosphorylation and growth of thyroid cancer in vitro and in vivo.

Mouse embryo fibroblasts lacking the tumor suppressor menin show altered expression of extracellular matrix protein genes.

Multiple Endocrine Neoplasia Type 1: Latest Insights

Multiple endocrine neoplasia type 1

Multiple endocrine neoplasia type 1 variant with frequent prolactinoma and rare gastrinoma

Multiple endocrine neoplasia type 1: new clinical and basic findings

Overexpression of a truncated growth hormone receptor in the sex-linked dwarf chicken: evidence for a splice mutation.

Parafibromin, product of the hyperparathyroidism-jaw tumor syndrome gene HRPT2, regulates cyclin D1/PRAD1 expression

Parathyroid tumor development involves deregulation of homeobox genes

Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1.

Pro-oncogenic Roles of HLXB9 Protein in Insulinoma Cells through Interaction with Nono Protein and Down-regulation of the c-Met Inhibitor Cblb (Casitas B-lineage Lymphoma b).

Probability of Positive Genetic Testing Results in Patients with Family History of Primary Hyperparathyroidism

Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states

Reoperative Surgery in Patients with Multiple Endocrine Neoplasia Type 1 Associated Primary Hyperparathyroidism.

Somatic mutation of the MEN1 gene in parathyroid tumours

Study of the multiple endocrine neoplasia type 1, growth hormone-releasing hormone receptor, Gs alpha, and Gi2 alpha genes in isolated familial acromegaly

The 32-kilodalton subunit of replication protein A interacts with menin, the product of the MEN1 tumor suppressor gene

The Long Non-Coding RNA MEG3 is an Epigenetic Determinant of Oncogenic Signaling in Functional Pancreatic Neuroendocrine Tumor Cells

The MEN1 gene and pituitary tumours.

The adenine phosphoribosyltransferase-encoding gene of Arabidopsis thaliana.

The embryonic transcription factor Hlxb9 is a menin interacting partner that controls pancreatic β-cell proliferation and the expression of insulin regulators

The future: genetics advances in MEN1 therapeutic approaches and management strategies.

The gene for multiple endocrine neoplasia type 1: recent findings.

The parafibromin tumor suppressor protein interacts with actin-binding proteins actinin-2 and actinin-3.

The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations

The tumor suppressor protein menin inhibits AKT activation by regulating its cellular localization.

Transcription factor JunD, deprived of menin, switches from growth suppressor to growth promoter

Transcriptional alterations in hereditary and sporadic nonfunctioning pancreatic neuroendocrine tumors according to genotype.