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Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapy

British journal of cancer, 2007-04, Vol.96 (8), p.1166-1169

2007

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TP53 mutations predict disease control in metastatic colorectal cancer treated with cetuximab-based chemotherapy

British journal of cancer, 2009-04, Vol.100 (8), p.1330-1335

2009

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Clinical interest of KRAS mutation detection in blood for anti-EGFR therapies in metastatic colorectal cancer

British journal of cancer, 2008-08, Vol.99 (3), p.551-552

2008

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High frequency in esophageal cancers of p53 alterations inactivating the regulation of genes involved in cell cycle and apoptosis

Carcinogenesis (New York), 2000-04, Vol.21 (4), p.563-565

2000

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IGF-1R Reduction Triggers Neuroprotective Signaling Pathways in Spinal Muscular Atrophy Mice

The Journal of neuroscience, 2015-08, Vol.35 (34), p.12063-12079

2015

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Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC

Journal of medical genetics, 2004-01, Vol.41 (1), p.18-20

2004

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Spatio‐temporal expression of MRF4 transcripts and protein during Xenopus laevis embryogenesis

Developmental dynamics, 2006-02, Vol.235 (2), p.524-529

2006

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Towards the Lowest Efficacious Dose: Results From a Multicenter Noninferiority Randomized Open‐Label Controlled Trial Assessing Tocilizumab or Abatacept Injection Spacing in Rheumatoid Arthritis in Remission

Arthritis & rheumatology (Hoboken, N.J.), 2024-04, Vol.76 (4), p.541-552

2024

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Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome

Journal of medical genetics, 2001-04, Vol.38 (4), p.253-256

2001

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Molecular basis of dopamine replacement therapy and its side effects in Parkinson’s disease

Cell and tissue research, 2018-07, Vol.373 (1), p.111-135

2018

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Detection of heterozygous SMN1 deletions in SMA families using a simple fluorescent multiplex PCR method

Journal of medical genetics, 2001-04, Vol.38 (4), p.240-243

2001

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The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease

Genomics (San Diego, Calif.), 1995-03, Vol.26 (2), p.254-257

1995

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New therapeutic approaches in 2014 in pulmonary medicine: COPD, asthma and lung fibrosis

Revue médicale suisse, 2015-01, Vol.11 (456-457), p.129

2015

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Energy, current, and success in defibrillation and cardioversion: clinical studies using an automated impedance-based method of energy adjustment

Circulation (New York, N.Y.), 1988-05, Vol.77 (5), p.1038-1046

1988

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MSH2 in contrast to MLH1 and MSH6 is frequently inactivated by exonic and promoter rearrangements in hereditary nonpolyposis colorectal cancer

Cancer research (Chicago, Ill.), 2002-02, Vol.62 (3), p.848-853

2002

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Genomic Organization of the Human SPOCK Gene and Its Chromosomal Localization to 5q31

Genomics (San Diego, Calif.), 1998-03, Vol.48 (3), p.377-380

1998

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Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments

Cancer research (Chicago, Ill.), 2000-06, Vol.60 (11), p.2760-2763

2000

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Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene

Oncogene, 2003-02, Vol.22 (6), p.840-846

2003

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Pulmonary medicine 2012: news for the general practitioner

Revue médicale suisse, 2013-01, Vol.9 (369), p.142

2013

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The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

Journal of neurology, neurosurgery and psychiatry, 2013-06, Vol.84 (6), p.666-673

2013

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Presenilins Interact with Rab11, a Small GTPase Involved in the Regulation of Vesicular Transport

Human molecular genetics, 1999-07, Vol.8 (7), p.1263-1269

1999

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Mutations of the presenilin I gene in families with early-onset Alzheimer's disease

Human molecular genetics, 1995-12, Vol.4 (12), p.2373-2377

1995

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Genomic organization and expression of the ubiquitin-proteasome complex-associated protein Rbx1/ROC1/Hrt1

Cellular and molecular biology (Noisy-le-Grand, France), 1999-12, Vol.45 (8), p.1131

1999

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Two myogenin-related genes are differentially expressed in Xenopus laevis myogenesis and differ in their ability to transactivate muscle structural genes

The Journal of biological chemistry, 2002-01, Vol.277 (2), p.1139-1147

2002

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Advance prediction of transthoracic impedance in human defibrillation and cardioversion: importance of impedance in determining the success of low-energy shocks

Circulation (New York, N.Y.), 1984-08, Vol.70 (2), p.303-308

1984

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Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapy

TP53 mutations predict disease control in metastatic colorectal cancer treated with cetuximab-based chemotherapy

Clinical interest of KRAS mutation detection in blood for anti-EGFR therapies in metastatic colorectal cancer

High frequency in esophageal cancers of p53 alterations inactivating the regulation of genes involved in cell cycle and apoptosis

IGF-1R Reduction Triggers Neuroprotective Signaling Pathways in Spinal Muscular Atrophy Mice

Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC

Spatio‐temporal expression of MRF4 transcripts and protein during Xenopus laevis embryogenesis

Towards the Lowest Efficacious Dose: Results From a Multicenter Noninferiority Randomized Open‐Label Controlled Trial Assessing Tocilizumab or Abatacept Injection Spacing in Rheumatoid Arthritis in Remission

Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome

Molecular basis of dopamine replacement therapy and its side effects in Parkinson’s disease

Detection of heterozygous SMN1 deletions in SMA families using a simple fluorescent multiplex PCR method

The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease

New therapeutic approaches in 2014 in pulmonary medicine: COPD, asthma and lung fibrosis

Energy, current, and success in defibrillation and cardioversion: clinical studies using an automated impedance-based method of energy adjustment

MSH2 in contrast to MLH1 and MSH6 is frequently inactivated by exonic and promoter rearrangements in hereditary nonpolyposis colorectal cancer

Genomic Organization of the Human SPOCK Gene and Its Chromosomal Localization to 5q31

Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments

Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene

Pulmonary medicine 2012: news for the general practitioner

The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

Presenilins Interact with Rab11, a Small GTPase Involved in the Regulation of Vesicular Transport

Mutations of the presenilin I gene in families with early-onset Alzheimer's disease

Genomic organization and expression of the ubiquitin-proteasome complex-associated protein Rbx1/ROC1/Hrt1

Two myogenin-related genes are differentially expressed in Xenopus laevis myogenesis and differ in their ability to transactivate muscle structural genes

Advance prediction of transthoracic impedance in human defibrillation and cardioversion: importance of impedance in determining the success of low-energy shocks

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