V. Moreau

发表

Identification of human p53 mutations with differential effects on the bax and p21 promoters using functional assays in yeast

R. Iggo, T. Frebourg, J. Flaman, 1998, Oncogene.

Alternative Splicing of MLH 1 Messenger RNA in Human Normal Cells 1

T. Frebourg, M. Scotté, Cosette Martin, 2006 .

Cells Messenger RNA in Human Normal MLH 1 Alternative Splicing of Updated

T. Frebourg, M. Scotté, Cosette Martin, 2006 .

Alternative splicing of MLH1 messenger RNA in human normal cells.

T. Frebourg, M. Scotté, Cosette Martin, 1995, Cancer research.

A rapid PCR fidelity assay.

R. Iggo, T. Frebourg, R. Iggo, 1994, Nucleic acids research.

A simple p 53 functional assay for screening cell lines , blood , and tumors ( tumor-suppressor gene / Li-Fraumeni syndrome / transcription factor / mutation detection / ADE 2 gene )

Erwin G. Van Meir, M. Tada, J. Benhattar, 2022 .

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

R. Heilig, D. Campion, D. Hannequin, 1995, Genomics.

De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.

Miguel Ángel Martínez, Y. Agid, D. Campion, 1998, Journal of medical genetics.

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

T. Frebourg, J. Borg, M. Vasse, 1995, British journal of haematology.

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

J. Mallet, D. Campion, S. Dollfus, 1996, Psychiatry Research.

A simple p53 functional assay for screening cell lines, blood, and tumors.

P. Chappuis, J. Benhattar, A. Sappino, 1995, Proceedings of the National Academy of Sciences of the United States of America.

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

B. Dubois, D. Campion, D. Hannequin, 1995, Human molecular genetics.

Identification of novel germline hMLH1 mutations including a 22 kb Alu-mediated deletion in patients with familial colorectal cancer.

T. Frebourg, J. Limacher, Cosette Martin, 1996, Cancer research.

A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years.

Y. Agid, M. Baulac, C. Duyckaerts, 1996, Neuroreport.