L. Forestier

发表

Mutations in the vasopressin V2 receptor and aquaporin-2 genes in 12 families with congenital nephrogenic diabetes insipidus.

C. Antignac, P. Niaudet, R. Vargas-Poussou, 1997, Journal of the American Society of Nephrology : JASN.

Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome.

C. Antignac, B. Knebelmann, J. Saus, 1995, Human molecular genetics.

CHI3L1, NTRK2, 1p/19q and IDH Status Predicts Prognosis in Glioma

F. Caire, L. Forestier, E. Deluche, 2019, Cancers.

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.

G. Mollet, C. Antignac, C. Antignac, 1998, American journal of human genetics.

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.

G. Mollet, C. Antignac, C. Antignac, 2001, Journal of the American Society of Nephrology : JASN.

Glycosylation-related gene expression profiling in the brain and spleen of scrapie-affected mouse.

H. Laude, A. Le Dur, L. Forestier, 2009, Glycobiology.

Deep Intronic Mutation and Pseudo Exon Activation as a Novel Muscular Hypertrophy Modifier in Cattle

L. Forestier, A. Oulmouden, G. Renand, 2014, PloS one.

Butyrate regulation of glycosylation-related gene expression: evidence for galectin-1 upregulation in human intestinal epithelial goblet cells.

V. Gouyer, G. Huet, C. Hoebler, 2004, Biochemical and biophysical research communications.

High concentration of cadmium induces AtPCS2 gene expression in Arabidopsis thaliana (L.) Heynh ecotype Wassilewskija seedlings

C. Riou, L. Forestier, V. Gloaguen, 2012, Acta Physiologiae Plantarum.

Perfusate Metabolomics Content and Expression of Tubular Transporters During Human Kidney Graft Preservation by Hypothermic Machine Perfusion

F. Bruyère, P. Marquet, L. Nadal-Desbarats, 2022, Transplantation.

Perfusate metabolomics content and tubular transporters expression during kidney graft preservation by hypothermic machine perfusion

F. Bruyère, P. Marquet, L. Nadal-Desbarats, 2021, medRxiv.

Mutations in the vasopressin V2 receptor and aquaporin-2 genes in twelve families with congenital nephrogenic diabetes insipidus.

C. Antignac, P. Niaudet, R. Vargas-Poussou, 1998, Advances in experimental medicine and biology.

A composite six bp in-frame deletion in the melanocortin 1 receptor (MC1R) gene is associated with the Japanese brindling coat colour in rabbits (Oryctolagus cuniculus)

L. Fontanesi, V. Russo, L. Forestier, 2010, BMC Genetics.

Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin.

C. Antignac, S. Cherqui, L. Forestier, 1999, Human molecular genetics.

PHEXL222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease

V. Blanquet, F. Di Meo, L. Forestier, 2022, Genes.

Overexpression of both full-length and truncated isoforms of bovine PGC-1alpha enhances myoblasts differentiation

V. Blanquet, L. Forestier, A. Parenté, 2019, Gene Reports.

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis

O. Gribouval, C. Antignac, G. Bates, 1998, Nature Genetics.

Identification and Characterisation of the Murine Homologue of the Gene Responsible for Cystinosis, Ctns

C. Antignac, S. Cherqui, L. Forestier, 2000, BMC Genomics.

Molecular characterization of CTNS deletions in nephropathic cystinosis: development of a PCR-based detection assay.

C. Antignac, S. Cherqui, L. Forestier, 1999, American journal of human genetics.

Post-transcriptional regulation of polymorphic Protease-activated receptor-2 (PAR-2) gene displaying correlation with skin pigmentation in cattle.

L. Forestier, H. Levéziel, A. Oulmouden, 2014 .

Glycosylation-related gene expression is linked to differentiation status in glioblastomas undifferentiated cells.

M. Cheray, L. Forestier, M. Jauberteau, 2011, Cancer letters.

Characterization of the rabbit agouti signaling protein (ASIP) gene: transcripts and phylogenetic analyses and identification of the causative mutation of the nonagouti black coat colour.

C. Vernesi, L. Fontanesi, V. Russo, 2010, Genomics.

The Blonde d'Aquitaine T3811>G3811 mutation in the myostatin gene: association with growth, carcass and muscle phenotypes in veal calves.

M. Bonnet, B. Picard, I. Cassar-Malek, 2021, Journal of animal science.

Characterization of the bovine PRKAG3 gene: structure, polymorphism, and alternative transcripts

A. Ouali, L. Forestier, H. Levéziel, 2006, Mammalian Genome.

Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome.

C. Antignac, C. Antignac, M. Gubler, 1996, American journal of human genetics.

Modulation of gene expression in CD4+ T lymphocytes following in vitro HIV infection: a comparison between human and chimpanzee

C. Pasquier, J. Izopet, A. Blancher, 2015, VirusDisease.

Glycosylation-related Gene Expression in Prion Diseases

L. Forestier, J. Deslys, R. Julien, 2005, Journal of Biological Chemistry.

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes.

A. Ziegler, K. Grzeschik, G. Rizzoni, 1997, Human molecular genetics.

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity

A. Ziegler, G. Rizzoni, C. Antignac, 2019 .

Pilot Study of Whole Blood MicroRNAs as Potential Tools for Diffuse Low-Grade Gliomas Detection

H. Duffau, R. Sabatier, C. Reynès, 2018, Cellular and Molecular Neurobiology.

Weathering of Sb-rich mining and smelting residues: Insight in solid speciation and soil bacteria toxicity

M. Kunz, F. Foucher, L. Forestier, 2012 .

Expression of SERPINA3s in cattle: focus on bovSERPINA3-7 reveals specific involvement in skeletal muscle

B. Picard, L. Forestier, A. Maftah, 2015, Open Biology.

Literature Abstracts

G. Mollet, M. Gubler, L. Forestier, 2001, Pediatric Nephrology.

High concentration of cadmium induces AtPCS2 gene expression in Arabidopsis thaliana (L.) Heynh ecotype Wassilewskija seedlings

C. Riou, L. Forestier, V. Gloaguen, 2012, Acta Physiologiae Plantarum.

An integrative method to normalize RNA-Seq data

R. Philippe, C. Klopp, L. Forestier, 2014, BMC Bioinformatics.

Modulation of gene expression in CD4+ T lymphocytes following in vitro HIV infection: a comparison between human and chimpanzee

C. Pasquier, J. Izopet, A. Blancher, 2015, VirusDisease.

Spectrum ofMutations intheCOL4A5Collagen GeneinX-Linked Alport Syndrome

C. Antignac, B. Knebelmann, G. Deschênes, 1996 .