P. Millasseau

发表

Identification and characterization of a spinal muscular atrophy-determining gene

J. Weissenbach, D. Paslier, A. Munnich, 1995, Cell.

Genetic and physiological data implicating the new human gene G72 and the gene for d-amino acid oxidase in schizophrenia

P. Sham, L. Cavarec, R. Straub, 2002, Proceedings of the National Academy of Sciences of the United States of America.

A second-generation linkage map of the human genome

G. Gyapay, J. Morissette, J. Weissenbach, 1992, Nature.

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

J. Weissenbach, D. Paslier, J. Claverie, 1991, Cell.

A comprehensive genetic map of the human genome based on 5,264 microsatellites

Cécile Fizames, Colette Dib, Jean Weissenbach, 1996, Nature.

E-box- and MEF-2-independent muscle-specific expression, positive autoregulation, and cross-activation of the chicken MyoD (CMD1) promoter reveal an indirect regulatory pathway

L. Bougueleret, P. Millasseau, B. Paterson, 1994, Molecular and cellular biology.

Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3.

J. Gécz, P. Millasseau, M. Khrestchatisky, 1994, Human molecular genetics.

Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcripts.

J. Gécz, P. Millasseau, L. Villard, 1993, Human molecular genetics.

The 1993–94 Généthon human genetic linkage map

Cécile Fizames, Colette Dib, Jean Weissenbach, 1994, Nature Genetics.

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.

P. Sham, L. Cavarec, R. Straub, 2002, Nature Reviews Genetics.

Isolation of 10 differentially expressed cDNAs in p53-induced apoptosis: activation of the vertebrate homologue of the drosophila seven in absentia gene.

D. Israeli, L. Cazes, L. Piouffre, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Down‐regulation of mitochondrial mRNAs in the mdx mouse model for Duchenne muscular dystrophy

J. Léger, P. Millasseau, C. Dechesne, 1995, FEBS letters.

Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders.

J. Weissenbach, H. Cann, S. Meier-Ewert, 1996, Human molecular genetics.

De novo and inherited deletions of the 5q13 region in spinal muscular atrophies.

D. Le Paslier, D. Paslier, M. Zeviani, 1994, Science.

Two DR beta allelic series defined by exon II-specific synthetic oligonucleotide genomic hybridization: a method of HLA typing?

J. Dausset, D. Cohen, P. Millasseau, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43.

W. Vogel, O. Cussenot, A. Valéri, 1998, American journal of human genetics.

Mutations in the Muscle Sodium Channel Gene (SCN4A) in 13 French Families with Hyperkalemic Periodic Paralysis and Paramyotonia Congenita: Phenotype to Genotype Correlations and Demonstration of the Predominance of Two Mutations

G. Serratrice, F. Chapon, C. Confavreux, 1994, European journal of human genetics : EJHG.

New methods for detection of HLA genes polymorphism useful for associated diseases studies.

P. Millasseau, A. Chaussé, P. Paul, 1986, Pathologie et biologie.

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia (vol 99, pg 13675, 2002)

P. Sham, L. Cavarec, R. Straub, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Illegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuria.

A. Munnich, S. Lyonnet, P. Millasseau, 1993, Human Molecular Genetics.