Molecular Genetics of Parathyroid Disease (original) (raw)

Aberrant WNT/β-catenin signaling in parathyroid carcinoma

Göran Åkerström

Molecular Cancer, 2010

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Β-Catenin Activation is Not Involved in Sporadic Parathyroid Carcinomas and Adenomas

elena pardi

Endocrine-Related Cancer, 2009

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Genetics and Epigenetics of Parathyroid Carcinoma

Giuliano Perigli

Frontiers in Endocrinology, 2022

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Gene Expression of Parathyroid Tumors: Molecular Subclassification and Identification of the Potential Malignant Phenotype

Bin Teh

2004

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A Family with Isolated Hyperparathyroidism Segregating a Missense MEN1 Mutation and Showing Loss of the Wild-Type Alleles in the Parathyroid Tumors

Bin Teh

The American Journal of Human Genetics, 1998

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Gene Expression of Parathyroid Tumors

Bruce Robinson

Cancer Research, 2004

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Genetic characterization of large parathyroid adenomas

Felix Haglund, Inga-lena Nilsson

Endocrine Related Cancer, 2012

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Catenin Activation is Not Involved in Sporadic Parathyroid Carcinomas and Adenomas

Filomena Cetani

Endocr Related Cancer, 2010

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Molecular Alterations in Sporadic Primary Hyperparathyroidism

Paula Soares

Genetics Research International, 2011

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Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas

Randall Gaz

Cancer research, 1996

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MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism

Paula Soares

European Journal of Endocrinology, 2012

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Genetic alterations in primary and secondary hyperparathyroidism

liang shan

Pathology International, 1998

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Parathyroid Tumors: Molecular Signatures

Francesca Giusti

International Journal of Molecular Sciences, 2021

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Complete genomic landscape of a recurring sporadic parathyroid carcinoma

Pawan Pandoh

The Journal of Pathology, 2013

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Alterations of the MEN1 Gene in Sporadic Parathyroid Tumors 1

K. Sandelin

The Journal of Clinical Endocrinology & Metabolism, 1998

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Independent Genetic Events Associated with the Development of Multiple Parathyroid Tumors in Patients with Primary Hyperparathyroidism

Diana Learoyd

The American Journal of Pathology, 2002

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HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

Bin Teh

Nature Genetics, 2002

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Specifying the molecular pattern of sporadic parathyroid tumorigenesis—The Y282D variant of the GCM2 gene

Isabella Boschin

Biomedicine & Pharmacotherapy, 2017

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Comprehensive Genomic Characterization of Parathyroid Cancer Identifies Novel Candidate Driver Mutations and Core Pathways

Lily Kwatampora

Journal of the Endocrine Society, 2018

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Patterns of Chromosomal Imbalances in Parathyroid Carcinomas

K. Sandelin

The American Journal of Pathology, 2000

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HRPT2gene analysis and the diagnosis of parathyroid carcinoma

Filomena Cetani

Expert Review of Endocrinology & Metabolism, 2008

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Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas

Gert Fleuren

Clinical Endocrinology, 2007

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Diagnosis, management, histology and genetics of sporadic primary hyperparathyroidism: old knowledge with new tricks

Fausto Palazzo

Endocrine connections, 2018

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Loss of heterozygosity of selected tumor suppressor genes in parathyroid carcinoma. Discussion

Julie Sosa, Linwah Yip

Surgery, 2008

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Loss of heterozygosity of selected tumor suppressor genes in parathyroid carcinoma

Orlo Clark

Surgery, 2008

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Molecular Profiling of Parathyroid Hyperplasia, Adenoma and Carcinoma

Gyula Végso

Pathology & Oncology Research, 2011

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Molecular Classification of Parathyroid Neoplasia by Gene Expression Profiling

Nita Williams

The American Journal of Pathology, 2004

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Allelic Loss in Parathyroid Tumors from Individuals Homozygous for Multiple Endocrine Neoplasia Type 1 1

Sergio Ortolani

The Journal of Clinical Endocrinology & Metabolism, 1997

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