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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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Phase II study of capecitabine and the oral mTOR inhibitor everolimus in patients with advanced pancreatic cancer

Cancer chemotherapy and pharmacology, 2015-06, Vol.75 (6), p.1135-1141

2015

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Deregulated expression of EZH2 in congenital brainstem disconnection

Neuropathology and applied neurobiology, 2017-06, Vol.43 (4), p.358-365

2017

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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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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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Cyclin E low molecular weight isoforms occur commonly in early-onset gastric cancer and independently predict survival

Journal of clinical pathology, 2008-03, Vol.61 (3), p.311-316

2008

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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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Peutz–Jeghers syndrome polyps are polyclonal with expanded progenitor cell compartment

Gut, 2007-10, Vol.56 (10), p.1475-1476

2007

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Adjuvant hepatic arterial infusion pump chemotherapy and resection versus resection alone in patients with low-risk resectable colorectal liver metastases - the multicenter randomized controlled PUMP trial

BMC cancer, 2019-04, Vol.19 (1), p.327-9, Article 327

2019

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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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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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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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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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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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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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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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Genomic structure, chromosomal localization, and embryonic expression of the mouse homolog of PRCC, a gene associated with papillary renal cell carcinoma

Cytogenetics and cell genetics, 2001, Vol.92 (3-4), p.326

2001

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Expression of calcyclin in human melanocytic lesions

Cancer research (Chicago, Ill.), 1993-12, Vol.53 (24), p.6061-6066

1993

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Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint

Cytogenetics and cell genetics, 1996, Vol.75 (1), p.2

1996

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Molecular markers of melanocytic tumor progression

Laboratory investigation, 1994-05, Vol.70 (5), p.593

1994

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

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

1996

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Deregulated expression of EZH2 in congenital brainstem disconnection

Neuropathology and applied neurobiology, 2017, Vol.43 (4), p.358-365

2017

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Thymosin β-10 expression in melonoma cell lines and melanocytic lesions : a new progression marker for human cutaneous melanoma

International journal of cancer, 1993, Vol.53 (2), p.278-284

1993

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Metformin in patients with advanced pancreatic cancer: a double-blind, randomised, placebo-controlled phase 2 trial

The lancet oncology, 2015-07, Vol.16 (7), p.839-847

2015

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A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy

Human molecular genetics, 2012-01, Vol.21 (2), p.358-370

2012

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

Phase II study of capecitabine and the oral mTOR inhibitor everolimus in patients with advanced pancreatic cancer

Deregulated expression of EZH2 in congenital brainstem disconnection

Phenotype of Charcot-Marie-Tooth disease Type 2

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

Cyclin E low molecular weight isoforms occur commonly in early-onset gastric cancer and independently predict survival

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

Peutz–Jeghers syndrome polyps are polyclonal with expanded progenitor cell compartment

Adjuvant hepatic arterial infusion pump chemotherapy and resection versus resection alone in patients with low-risk resectable colorectal liver metastases - the multicenter randomized controlled PUMP trial

STRAD in Peutz-Jeghers syndrome and sporadic cancers

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

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

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

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

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

Increasing Epidermal Growth Factor Receptor Expression in Human Melanocytic Tumor Progression

Genomic structure, chromosomal localization, and embryonic expression of the mouse homolog of PRCC, a gene associated with papillary renal cell carcinoma

Expression of calcyclin in human melanocytic lesions

Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint

Molecular markers of melanocytic tumor progression

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

Deregulated expression of EZH2 in congenital brainstem disconnection

Thymosin β-10 expression in melonoma cell lines and melanocytic lesions : a new progression marker for human cutaneous melanoma

Metformin in patients with advanced pancreatic cancer: a double-blind, randomised, placebo-controlled phase 2 trial

A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy

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