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Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene

Neurology, 2006-10, Vol.67 (8), p.1476

2006

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Phenotype of Charcot-Marie-Tooth disease Type 2

Neurology, 2007-05, Vol.68 (20), p.1658

2007

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Fusion of the Transcription Factor TFE3 Gene to a Novel Gene, PRCC, in t(X;1) (p11;q21)-Positive Papillary Renal Cell Carcinomas

Proceedings of the National Academy of Sciences - PNAS, 1996-12, Vol.93 (26), p.15294-15298

1996

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Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

Clinical genetics, 2007-12, Vol.72 (6), p.568-573

2007

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Exclusion of RUNX3 as a tumour-suppressor gene in early-onset gastric carcinomas

Oncogene, 2005-12, Vol.24 (56), p.8252-8258

2005

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Understanding familial and non-familial renal cell cancer

Human molecular genetics, 2002-10, Vol.11 (20), p.2489-2498

2002

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Impairment of MAD2B-PRCC Interaction in Mitotic Checkpoint Defective t(X;1)-Positive Renal Cell Carcinomas

Proceedings of the National Academy of Sciences - PNAS, 2001-11, Vol.98 (24), p.13808-13813

2001

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Early-onset gastric carcinomas display molecular characteristics distinct from gastric carcinomas occurring at a later age

The Journal of pathology, 2004-09, Vol.204 (1), p.75-83

2004

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Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas

Cancer research (Chicago, Ill.), 2001-05, Vol.61 (10), p.4130-4135

2001

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Different Pattern of Allelic Loss in Epstein-Barr Virus-Positive Gastric Cancer with Emphasis on the p53 Tumor Suppressor Pathway

The American journal of pathology, 2002-10, Vol.161 (4), p.1207-1213

2002

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Nuclear localization and transactivating capacities of the papillary renal cell carcinoma-associated TFE3 and PRCC (fusion) proteins

Oncogene, 2000-01, Vol.19 (1), p.69-74

2000

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Cyclooxygenase 2 Expression and Molecular Alterations in Peutz-Jeghers Hamartomas and Carcinomas

Clinical cancer research, 2003-08, Vol.9 (8), p.3065-3072

2003

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nmb, a novel gene, is expressed in low‐metastatic human melanoma cell lines and xenografts

International journal of cancer, 1995-01, Vol.60 (1), p.73-81

1995

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Ductuloinsular tumors of the pancreas: Endocrine tumors with entrapped nonneoplastic ductules

The American journal of surgical pathology, 2004-06, Vol.28 (6), p.813-820

2004

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STRAD in Peutz-Jeghers syndrome and sporadic cancers

Journal of clinical pathology, 2005-10, Vol.58 (10), p.1091-1095

2005

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Transformation capacities of the papillary renal cell carcinoma-associated PRCCTFE3 and TFE3PRCC fusion genes

Oncogene, 2001-03, Vol.20 (12), p.1414-1424

2001

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An Alternative Route for Multistep Tumorigenesis in a Novel Case of Hereditary Renal Cell Cancer and a t(2;3)(q35;q21) Chromosome Translocation

American journal of human genetics, 1998-06, Vol.62 (6), p.1475-1483

1998

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Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)

Genes chromosomes & cancer, 2001-05, Vol.31 (1), p.23-32

2001

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Expression of calcyclin in human melanoma cell lines correlates with metastatic behavior in nude mice

Cancer research (Chicago, Ill.), 1992-03, Vol.52 (5), p.1291-1296

1992

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Short Report: Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

Clinical genetics, 2007-12, Vol.72 (6), p.568

2007

Volltextzugriff (PDF)

Molecular genetic evidence of an association between nasal polyposis and the Peutz-Jeghers syndrome

Annals of internal medicine, 2002-06, Vol.136 (11), p.855

2002

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Expression of nma, a novel gene, inversely correlates with the metastatic potential of human melanoma cell lines and xenografts

International journal of cancer, 1996-02, Vol.65 (4), p.460-465

1996

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Pancreatic Endocrine Tumors With Ductules

The American journal of surgical pathology, 2005-01, Vol.29 (1), p.137-138

2005

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Increasing Epidermal Growth Factor Receptor Expression in Human Melanocytic Tumor Progression

Journal of investigative dermatology, 1992-08, Vol.99 (2), p.168-173

1992

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Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation

Human genetics, 1996-07, Vol.98 (1), p.16-21

1996

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Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene

Phenotype of Charcot-Marie-Tooth disease Type 2

Fusion of the Transcription Factor TFE3 Gene to a Novel Gene, PRCC, in t(X;1) (p11;q21)-Positive Papillary Renal Cell Carcinomas

Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

Exclusion of RUNX3 as a tumour-suppressor gene in early-onset gastric carcinomas

Understanding familial and non-familial renal cell cancer

Impairment of MAD2B-PRCC Interaction in Mitotic Checkpoint Defective t(X;1)-Positive Renal Cell Carcinomas

Early-onset gastric carcinomas display molecular characteristics distinct from gastric carcinomas occurring at a later age

Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25.3)-bearing papillary renal cell carcinomas

Different Pattern of Allelic Loss in Epstein-Barr Virus-Positive Gastric Cancer with Emphasis on the p53 Tumor Suppressor Pathway

Nuclear localization and transactivating capacities of the papillary renal cell carcinoma-associated TFE3 and PRCC (fusion) proteins

Cyclooxygenase 2 Expression and Molecular Alterations in Peutz-Jeghers Hamartomas and Carcinomas

nmb, a novel gene, is expressed in low‐metastatic human melanoma cell lines and xenografts

Ductuloinsular tumors of the pancreas: Endocrine tumors with entrapped nonneoplastic ductules

STRAD in Peutz-Jeghers syndrome and sporadic cancers

Transformation capacities of the papillary renal cell carcinoma-associated PRCCTFE3 and TFE3PRCC fusion genes

An Alternative Route for Multistep Tumorigenesis in a Novel Case of Hereditary Renal Cell Cancer and a t(2;3)(q35;q21) Chromosome Translocation

Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)

Expression of calcyclin in human melanoma cell lines correlates with metastatic behavior in nude mice

Short Report: Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates

Molecular genetic evidence of an association between nasal polyposis and the Peutz-Jeghers syndrome

Expression of nma, a novel gene, inversely correlates with the metastatic potential of human melanoma cell lines and xenografts

Pancreatic Endocrine Tumors With Ductules

Increasing Epidermal Growth Factor Receptor Expression in Human Melanocytic Tumor Progression

Fine mapping of the 1q21 breakpoint of the papillary renal cell carcinoma-associated (X;1) translocation

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