P. Miniou

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The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease.

A. Munnich, J. Melki, S. Lefebvre, 1997, American journal of human genetics.

Cloning and characterization of p 52 , the fifth subunit of the core of the transcription / DNA repair factor TFIIH experiments using normal and NER-deficient mammalian

J. Hoeijmakers, W. Vermeulen, J. Egly, 2013 .

Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH

J. Hoeijmakers, W. Vermeulen, J. Egly, 1997, The EMBO journal.

Human colorectal cancer (CRC) antigen CO17-1A/GA733 encoded by adenovirus inhibits growth of established CRC cells in mice.

R. Ricciardi, É. Gönczöl, H. Maruyama, 1997, Journal of immunology.

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.

A. Niveleau, D. Bonneau, V. Blanquet, 1994, Human molecular genetics.

Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice

F. Baas, Yunhong Bai, M. Shy, 2021, Molecular Neurobiology.

α-Satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

D. Bourc’his, V. Blanquet, E. Viégas-Péquignot, 1997, Human Genetics.

Baculovirus recombinant expressing a secreted form of a transmembrane carcinoma-associated antigen.

C. Strassburg, H. Koprowski, B. A. Seng, 1992, Cancer research.

Therapeutic Development in Charcot Marie Tooth Type 1 Disease

M. Fontès, P. Miniou, 2021, International journal of molecular sciences.

Undermethylation of Alu sequences in ICF syndrome: molecular and in situ analysis.

D. Bourc’his, E. Viégas-Péquignot, D. Molina Gomes, 1997, Cytogenetics and cell genetics.

Gene targeting restricted to mouse striated muscle lineage.

J. Melki, N. Roblot, M. L. Meur, 1999, Nucleic acids research.

Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy.

P Miniou, J. Melki, A. Dierich, 2000, Human molecular genetics.

The promoters of the survival motor neuron gene (SMN) and its copy (SMNc) share common regulatory elements.

J. Melki, A. Echaniz-Laguna, D. Bartholdi, 1999, American journal of human genetics.

Assignment of the human syntaxin 1B gene (STX) to chromosome 16p11.2 by fluorescence in situ hybridization.

J. Mallet, T. Smirnova, E. Viégas-Péquignot, 1996, Genomics.

Abnormal methylation does not prevent X inactivation in ICF patients

D. Bourc’his, J. Dupont, L. Tiepolo, 1999, Cytogenetic and Genome Research.

The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease.

A. Munnich, S. Lefebvre, P. Burlet, 1997, American journal of human genetics.

Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1.

H. Dollfus, S. Pittler, E. Viégas-Péquignot, 1994, Genomics.

cDNA, gene structure, and chromosomal localization of human GAR1 (CNCG3L), a homolog of the third subunit of bovine photoreceptor cGMP-gated channel.

S. Pittler, E. Viégas-Péquignot, L. Oliveira, 1995, Genomics.

A Rat Model of Clinically Relevant Extracorporeal Circulation Develops Early Organ Dysfunctions

B. Rozec, B. Lauzier, V. Aillerie, 2023, International journal of molecular sciences.