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Type II EATL (epitheliotropic intestinal T-cell lymphoma): a neoplasm of intra-epithelial T-cells with predominant CD8αα phenotype

Leukemia, 2013-08, Vol.27 (8), p.1688-1696

2013

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High-resolution profiling of histone h3 lysine 36 trimethylation in metastatic renal cell carcinoma

Oncogene, 2016-03, Vol.35 (12), p.1565-1574

2016

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

Nature genetics, 2002-12, Vol.32 (4), p.676-680

2002

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Role of eIF3a in regulating cisplatin sensitivity and in translational control of nucleotide excision repair of nasopharyngeal carcinoma

Oncogene, 2011-12, Vol.30 (48), p.4814-4823

2011

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HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours

Journal of medical genetics, 2003-09, Vol.40 (9), p.657-663

2003

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Clinical and genetic studies of Birt-Hogg-Dubé syndrome

Journal of medical genetics, 2002-12, Vol.39 (12), p.906-912

2002

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Nuclear expression of MATK is a novel marker of type II enteropathy-associated T-cell lymphoma

Leukemia, 2011-03, Vol.25 (3), p.555-557

2011

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Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications

Journal of medical genetics, 2004-03, Vol.41 (3), p.155-160

2004

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Hyperparathyroidism‐jaw tumour syndrome

Journal of internal medicine, 2003-06, Vol.253 (6), p.634-642

2003

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

Clinical endocrinology (Oxford), 2007-09, Vol.67 (3), p.370-376

2007

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Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinoma

British journal of cancer, 2008-01, Vol.98 (2), p.496-501

2008

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Functional studies of the MEN1 gene

Journal of internal medicine, 2003-06, Vol.253 (6), p.606-615

2003

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JAK-STAT and G-protein-coupled receptor signaling pathways are frequently altered in epitheliotropic intestinal T-cell lymphoma

Leukemia, 2016-06, Vol.30 (6), p.1311-1319

2016

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Microarray profiling of the effects of histone deacetylase inhibitors on gene expression in cancer cell lines

International journal of oncology, 2004-04, Vol.24 (4), p.773

2004

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Novel association of thymic carcinoid with a germline mutation in a kindred with multiple endocrine neoplasia 1 (MEN1)

Experimental and clinical endocrinology & diabetes, 2012-05, Vol.120 (5), p.257

2012

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Parafibromin expression in breast cancer: a novel marker for prognostication?

Journal of clinical pathology, 2008-01, Vol.61 (1), p.64-67

2008

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Thymic carcinoid in multiple endocrine neoplasia 1: genotype–phenotype correlation and prevention

Journal of internal medicine, 2006-04, Vol.259 (4), p.428-432

2006

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Oncogenic activation of JAK3-STAT signaling confers clinical sensitivity to PRN371, a novel selective and potent JAK3 inhibitor, in natural killer/T-cell lymphoma

Leukemia, 2018-05, Vol.32 (5), p.1147-1156

2018

Volltextzugriff (PDF)

Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndrome

Oncogene, 2017-07, Vol.36 (28), p.4025-4036

2017

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Thymic carcinoids in multiple endocrine neoplasia type 1

Journal of internal medicine, 1998-06, Vol.243 (6), p.501-504

TEH, B. T

1998

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Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism

The journal of clinical endocrinology and metabolism, 1998-08, Vol.83 (8), p.2621-2626

1998

Volltextzugriff (PDF)

Mutational Signatures in Mandibular Ameloblastoma Correlate with Smoking

Journal of dental research, 2019-06, Vol.98 (6), p.652-658

2019

Volltextzugriff (PDF)

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families

The journal of clinical endocrinology and metabolism, 1998-06, Vol.83 (6), p.2114-2120

1998

Volltextzugriff (PDF)

Towards a global cancer knowledge network: dissecting the current international cancer genomic sequencing landscape

Annals of oncology, 2017-05, Vol.28 (5), p.1145-1151

2017

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Genome-wide scan identifies novel modifier loci of acromegalic phenotypes for isolated familial somatotropinoma

Endocrine-related cancer, 2009-09, Vol.16 (3), p.1057-1063

2009

Volltextzugriff (PDF)

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Type II EATL (epitheliotropic intestinal T-cell lymphoma): a neoplasm of intra-epithelial T-cells with predominant CD8αα phenotype

High-resolution profiling of histone h3 lysine 36 trimethylation in metastatic renal cell carcinoma

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

Role of eIF3a in regulating cisplatin sensitivity and in translational control of nucleotide excision repair of nasopharyngeal carcinoma

HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours

Clinical and genetic studies of Birt-Hogg-Dubé syndrome

Nuclear expression of MATK is a novel marker of type II enteropathy-associated T-cell lymphoma

Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications

Hyperparathyroidism‐jaw tumour syndrome

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

Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinoma

Functional studies of the MEN1 gene

JAK-STAT and G-protein-coupled receptor signaling pathways are frequently altered in epitheliotropic intestinal T-cell lymphoma

Microarray profiling of the effects of histone deacetylase inhibitors on gene expression in cancer cell lines

Novel association of thymic carcinoid with a germline mutation in a kindred with multiple endocrine neoplasia 1 (MEN1)

Parafibromin expression in breast cancer: a novel marker for prognostication?

Thymic carcinoid in multiple endocrine neoplasia 1: genotype–phenotype correlation and prevention

Oncogenic activation of JAK3-STAT signaling confers clinical sensitivity to PRN371, a novel selective and potent JAK3 inhibitor, in natural killer/T-cell lymphoma

Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndrome

Thymic carcinoids in multiple endocrine neoplasia type 1

Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism

Mutational Signatures in Mandibular Ameloblastoma Correlate with Smoking

Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families

Towards a global cancer knowledge network: dissecting the current international cancer genomic sequencing landscape

Genome-wide scan identifies novel modifier loci of acromegalic phenotypes for isolated familial somatotropinoma

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