P. Lalle

发表

Definition of a Short Region of XPG Necessary for TFIIH Interaction and Stable Recruitment to Sites of UV Damage

R. Wood, A. Constantinou, W. Vermeulen, 2004, Molecular and Cellular Biology.

A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function.

S. A. Leadon, S. Clarkson, T. Nouspikel, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Nrh, a human homologue of Nr-13 associates with Bcl-Xs and is an inhibitor of apoptosis

M. Gouy, G. Gillet, D. Rigal, 2001, Oncogene.

Impact of hypoxia on the double-strand break repair after photon and carbon ion irradiation of radioresistant HNSCC cells

M. Beuve, P. Lalle, C. Rodriguez-Lafrasse, 2020, Scientific Reports.

Differential pattern of HIF-1α expression in HNSCC cancer stem cells after carbon ion or photon irradiation: one molecular explanation of the oxygen effect

N. Magné, M. Beuve, E. Blond, 2017, British Journal of Cancer.

Linkage analysis of 19 French breast cancer families, with five chromosome 17q markers.

B. Dutrillaux, S. Mazoyer, Y. Bignon, 1993, American journal of human genetics.

Modulation of Nr-13 antideath activity by peptide aptamers

G. Gillet, P. Colas, P. Lalle, 2007, Oncogene.

Lack of germ-line mutations in the p53 gene exons 4 to 8 in patients with late-onset second malignant neoplasms.

Y. Bignon, P. Lalle, C. Moyret, 1994, Cancer genetics and cytogenetics.

Modulating mitochondria-mediated apoptotic cell death through targeting of Bcl-2 family proteins.

G. Gillet, P. Lalle, A. Aouacheria, 2007, Recent patents on DNA & gene sequences.

High allele loss rates at I7q I2‐q2I in breast and ovarian tumors from BRCAI‐linked families

J. Chang-Claude, B. Ponder, C. Larsson, 1995 .

Detection of allelic losses on 17q12-q21 chromosomal region in benign lesions and malignant tumors occurring in a familial context.

M. D. De Latour, Y. Bignon, P. Lalle, 1994, Oncogene.

Evidence for crucial electrostatic interactions between Bcl-2 homology domains BH3 and BH4 in the anti-apoptotic Nr-13 protein.

M. Jambon, G. Deléage, C. Geourjon, 2002, The Biochemical journal.

Oocytes and early embryos selectively express the survival factor BCL2L10

G. Gillet, P. Lalle, J. Guérin, 2009, Journal of Molecular Medicine.

Genomic stability and wild-type p53 function of lymphoblastoid cells with germ-line p53 mutation.

M. Ozturk, C. Moyret-Lalle, Q. Wang, 1995, Oncogene.

Conserved Residues of Human XPG Protein Important for Nuclease Activity and Function in Nucleotide Excision Repair*

P. Bates, R. Wood, A. Constantinou, 1999, The Journal of Biological Chemistry.

The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity.

A. Constantinou, S. Clarkson, T. Nouspikel, 2002, The Journal of investigative dermatology.

Two germ-line mutations affecting the same nucleotide at codon 257 of p53 gene, a rare site for mutations.

S. Schraub, D. Frappaz, S. Mazoyer, 1994, Oncogene.

High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium.

B. Ponder, P. Tonin, D. Kelsell, 1995, Genes, chromosomes & cancer.