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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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A randomized double-blind placebo-controlled trial of low-dose interleukin-2 in relapsing–remitting multiple sclerosis

Journal of neurology, 2023-09, Vol.270 (9), p.4403-4414

2023

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Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism

Human molecular genetics, 1998-10, Vol.7 (11), p.1825-1829

1998

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A Simple p53 Functional Assay for Screening Cell Lines, Blood, and Tumors

Proceedings of the National Academy of Sciences - PNAS, 1995-04, Vol.92 (9), p.3963-3967

1995

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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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Citalopram versus fluoxetine: a double-blind, controlled, multicentre, phase III trial in patients with unipolar major depression treated in general practice

International clinical psychopharmacology, 1996-06, Vol.11 (2), p.129-136

1996

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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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Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

American journal of human genetics, 1999-09, Vol.65 (3), p.664-670

1999

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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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Regular Exercise Prolongs Survival in a Type 2 Spinal Muscular Atrophy Model Mouse

The Journal of neuroscience, 2005-08, Vol.25 (33), p.7615-7622

2005

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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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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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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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Early-Onset Brain Tumor and Lymphoma in MSH2-Deficient Children

American journal of human genetics, 2003, Vol.72 (1), p.213-216

2003

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HIV/AIDS prevention in the school setting: practices of biology teachers in France and in the Congo

Santé publique (Vandoeuvre-lès-Nancy, France), 2005-06, Vol.17 (2), p.211

2005

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Structure and cellular distribution of mouse brain testican. Association with the postsynaptic area of hippocampus pyramidal cells

The Journal of biological chemistry, 1996-02, Vol.271 (8), p.4373-4380

1996

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No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia

European journal of human genetics : EJHG, 1999-02, Vol.7 (2), p.247-250

1999

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Factors affecting transthoracic impedance during electrical cardioversion

The American journal of cardiology, 1988-11, Vol.62 (16), p.1048-1052

1988

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Association study between schizophrenia and monoamine oxidase A and B DNA polymorphisms

Psychiatry research, 1996-06, Vol.62 (3), p.221-226

1996

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Co‐segregation of thrombosis with the factor V Q506 mutation in an extended family with resistance to activated protein C

British journal of haematology, 1995-03, Vol.89 (3), p.659-662

1995

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No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group

Journal of medical genetics, 1996-08, Vol.33 (8), p.661-664

1996

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Citalopram and Viloxazine in the treatment of depression by means of slow drop infusion: A double-blind comparative trial

Journal of affective disorders, 1997-10, Vol.46 (1), p.51-58

1997

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Retrospective study of 935 sessions of electroconvulsive therapy (1989-91)

Annales médico psychologiques, 1992-12, Vol.150 (10), p.730-3; discussion 733-4

1992

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Descriptive study of schizophrenic patients treated for 15 years in the psychiatric department B of the Clermont-Ferrand C.H.U

Annales médico psychologiques, 1993-04, Vol.151 (4), p.307-309

1993

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

A randomized double-blind placebo-controlled trial of low-dose interleukin-2 in relapsing–remitting multiple sclerosis

Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism

A Simple p53 Functional Assay for Screening Cell Lines, Blood, and Tumors

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

Citalopram versus fluoxetine: a double-blind, controlled, multicentre, phase III trial in patients with unipolar major depression treated in general practice

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

Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

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

Regular Exercise Prolongs Survival in a Type 2 Spinal Muscular Atrophy Model Mouse

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

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

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

Early-Onset Brain Tumor and Lymphoma in MSH2-Deficient Children

HIV/AIDS prevention in the school setting: practices of biology teachers in France and in the Congo

Structure and cellular distribution of mouse brain testican. Association with the postsynaptic area of hippocampus pyramidal cells

No evidence for involvement of KCNN3 (hSKCa3) potassium channel gene in familial and isolated cases of schizophrenia

Factors affecting transthoracic impedance during electrical cardioversion

Association study between schizophrenia and monoamine oxidase A and B DNA polymorphisms

Co‐segregation of thrombosis with the factor V Q506 mutation in an extended family with resistance to activated protein C

No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group

Citalopram and Viloxazine in the treatment of depression by means of slow drop infusion: A double-blind comparative trial

Retrospective study of 935 sessions of electroconvulsive therapy (1989-91)

Descriptive study of schizophrenic patients treated for 15 years in the psychiatric department B of the Clermont-Ferrand C.H.U

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