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A Unified Nomenclature for the Superfamily of TRP Cation Channels

Molecular cell, 2002-02, Vol.9 (2), p.229-231

2002

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A family-based investigation of cold pain tolerance

Pain (Amsterdam), 2008-08, Vol.138 (1), p.111-118

2008

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Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression

Human molecular genetics, 2000-01, Vol.9 (2), p.203-216

2000

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TRPM5 Is a Transient Ca2+-Activated Cation Channel Responding to Rapid Changes in [ Ca2+]i

Proceedings of the National Academy of Sciences - PNAS, 2003-12, Vol.100 (25), p.15166-15171

2003

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RNAi knock-down mice: an emerging technology for post-genomic functional genetics

Cytogenetic and Genome Research, 2004-01, Vol.105 (2-4), p.412-421

2004

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Trastuzumab therapy vs tetracycline controlled ERBB2 downregulation: influence on tumour development in an ERBB2-dependent mouse tumour model

British journal of cancer, 2008-05, Vol.98 (9), p.1525-1532

2008

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Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives

Endocrine Connections, 2022-11, Vol.11 (11), p.1-14

2022

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Authors’ response to “Alternatively spliced human catechol- O -methyltransferase (COMT) rationalizes lack of Val158Met effects on pain tolerance”

Pain (Amsterdam), 2008-06, Vol.136 (3), p.446-447

2008

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Oncogene-Blocking Therapies: New Insights from Conditional Mouse Tumor Models

Current cancer drug targets, 2006-11, Vol.6 (7), p.603-612

2006

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Microdeletion of Target Sites for Insulator Protein CTCF in a Chromosome 11p15 Imprinting Center in Beckwith-Wiedemann Syndrome and Wilms' Tumor

Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (11), p.4085-4090

2005

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4-Epidoxycycline: an alternative to doxycycline to control gene expression in conditional mouse models

Biochemical and biophysical research communications, 2004-10, Vol.323 (3), p.979-986

2004

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Beckwith-Wiedemann-Syndrom

Medizinische Genetik, 2010-12, Vol.22 (4), p.399-404

2010

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Beckwith-Wiedemann-Syndrom

Medizinische Genetik, 2010-12, Vol.22 (4), p.399-404

2010

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The Influence of Decision Aids on User Behavior: Implications for Knowledge Acquisition and Inappropriate Reliance

Organizational behavior and human decision processes, 1997-11, Vol.72 (2), p.232-255

1997

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Systematic Screening of an Arrayed cDNA Library by PCR

Proceedings of the National Academy of Sciences - PNAS, 1995-03, Vol.92 (6), p.2209-2213

1995

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ERBB2-Mediated Transcriptional Up-regulation of the alpha 5 beta 1 Integrin Fibronectin Receptor Promotes Tumor Cell Survival Under Adverse Conditions

Cancer research (Chicago, Ill.), 2006-04, Vol.66 (7), p.3715-3725

2006

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Premature senescence is a primary fail-safe mechanism of erbb2-driven tumorigenesis in breast carcinoma cells

Cancer research (Chicago, Ill.), 2005-02, Vol.65 (3), p.840-849

2005

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The Wilms’ Tumor Suppressor Gene (wt1) Product Regulates Dax-1 Gene Expression during Gonadal Differentiation

Molecular and Cellular Biology, 1999-03, Vol.19 (3), p.2289-2299

1999

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Linking C5 Deficiency to an Exonic Splicing Enhancer Mutation

The Journal of immunology (1950), 2005-04, Vol.174 (7), p.4172-4177

2005

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Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

Nature genetics, 2005-08, Vol.37 (8), p.785-786

2005

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Switching off HER-2/neu in a tetracycline-controlled mouse tumor model leads to apoptosis and tumor-size-dependent remission

Cancer research (Chicago, Ill.), 2003-11, Vol.63 (21), p.7221-7231

2003

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Comparative architectural aspects of regions of conserved synteny on human chromosome 11p15.3 and mouse chromosome 7 (including genes WEE1 and LMO1)

Cytogenetic and genome research, 2001-01, Vol.93 (3-4), p.277-283

2001

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Linking C5 deficiency to an exonic splicing enhancer mutation

The Journal of immunology (1950), 2009-04, Vol.182 (8), p.5152-5152

2009

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Allelic loss but absence of mutations in the polyspecific transporter gene BWR1A on 11p15.5 in hepatoblastoma

International journal of cancer, 2004-09, Vol.111 (4), p.627-632

2004

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A Unified Nomenclature for the Superfamily of TRP Cation Channels

A family-based investigation of cold pain tolerance

Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression

TRPM5 Is a Transient Ca2+-Activated Cation Channel Responding to Rapid Changes in [ Ca2+]i

RNAi knock-down mice: an emerging technology for post-genomic functional genetics

Trastuzumab therapy vs tetracycline controlled ERBB2 downregulation: influence on tumour development in an ERBB2-dependent mouse tumour model

Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives

Authors’ response to “Alternatively spliced human catechol- O -methyltransferase (COMT) rationalizes lack of Val158Met effects on pain tolerance”

Oncogene-Blocking Therapies: New Insights from Conditional Mouse Tumor Models

Microdeletion of Target Sites for Insulator Protein CTCF in a Chromosome 11p15 Imprinting Center in Beckwith-Wiedemann Syndrome and Wilms' Tumor

4-Epidoxycycline: an alternative to doxycycline to control gene expression in conditional mouse models

Beckwith-Wiedemann-Syndrom

Beckwith-Wiedemann-Syndrom

The Influence of Decision Aids on User Behavior: Implications for Knowledge Acquisition and Inappropriate Reliance

Systematic Screening of an Arrayed cDNA Library by PCR

ERBB2-Mediated Transcriptional Up-regulation of the alpha 5 beta 1 Integrin Fibronectin Receptor Promotes Tumor Cell Survival Under Adverse Conditions

Premature senescence is a primary fail-safe mechanism of erbb2-driven tumorigenesis in breast carcinoma cells

The Wilms’ Tumor Suppressor Gene (wt1) Product Regulates Dax-1 Gene Expression during Gonadal Differentiation

Linking C5 Deficiency to an Exonic Splicing Enhancer Mutation

Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement

Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

Switching off HER-2/neu in a tetracycline-controlled mouse tumor model leads to apoptosis and tumor-size-dependent remission

Comparative architectural aspects of regions of conserved synteny on human chromosome 11p15.3 and mouse chromosome 7 (including genes WEE1 and LMO1)

Linking C5 deficiency to an exonic splicing enhancer mutation

Allelic loss but absence of mutations in the polyspecific transporter gene BWR1A on 11p15.5 in hepatoblastoma

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