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Publications d'autres sujets

Année 2010

- Association of insulin receptor genetic variants with polycystic ovary syndrome in a population of women from Central Europe.

- Winchester syndrome: the progression of radiological findings over a 23-year period.

- EGFR immunolabeling pattern may discriminate low-grade gliomas from gliosis.

- Infant coma in emergency department: 2 cases of MCAD deficiency

- Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients.

- Fatal case of Reye's syndrome associated with H3N2 influenza virus infection and salicylates intake in a 12 year-old patient.

- Chorea-acanthocytosis without acanthocytes


Année 2009

- Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.

- TRBP control of PACT-induced phosphorylation of protein kinase R is reversed by stress.

- Association of the FTO gene with obesity and the metabolic syndrome is independent of the IRS-2 gene in the female population of Southern France.

- LMNA, ZMPSTE24, and LBR are not mutated in scleroderma.

- TRBP control of PACT-induced phosphorylation of protein kinase R is reversed by stress.

- Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.


Année 2008

- Late cerebellar ataxia associated with fragile X permutation

- Diagnostic and prognostic values of 1p and 19q deletions in adult gliomas: critical review of the literature and implications in daily clinical practice

- Detection of the TMPRSS2-ETS fusion gene in prostate carcinomas: retrospective analysis of 55 formalin-fixed and paraffin-embedded samples with clinical data.

- Ovarian dysgerminoma and Apert syndrome.

- Presence of anti-Lepp12 antibody: a marker for diagnostic and prognostic evaluation of visceral leishmaniasis.

- Feasibility of nasal epithelial brushing for the study of airway epithelial functions in CF infants.


Année 2007

- CRM1-dependent nuclear export and dimerization with hMSH5 contribute to the regulation of hMSH4 subcellular localization.

- Identification of novel mutations in WFS1 and genotype-phenotype correlation in Wolfram syndrome.

- Newborn of HIV positive grandmother: reasons to be delighted or reasons to worry?

- Microvascular diabetes complications in Wolfram syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness [DIDMOAD]): an age- and duration-matched comparison with common type 1 diabetes.

- DNA extraction by FTA technology: application for rapid detection of 1p/19q deletions in gliomas.

- Neurosarcoidosis treated with mycophenolate mofetil: two cases

- Small interfering RNAs against the TAR RNA binding protein, TRBP, a Dicer cofactor, inhibit human immunodeficiency virus type 1 long terminal repeat expression and viral production. - Wolfram's syndrome presenting as a cerebellar ataxia

Année 2006

- A novel homozygous MMP2 mutation in a family with Winchester syndrome.

- Downregulation by a long-acting beta2-adrenergic receptor agonist and corticosteroid of Staphylococcus aureus-induced airway epithelial inflammatory mediator production.

- Leishmania proteins derived from recombinant DNA: current status and next steps.

- Cell-specific regulation of TRBP1 promoter by NF-Y transcription factor in lymphocytes and astrocytes.


Année 2005

- Low TRBP levels support an innate human immunodeficiency virus type 1 resistance in astrocytes by enhancing the PKR antiviral response.

- Recombinant DNA-derived leishmania proteins: from the laboratory to the field.

- HIV-1 TAR RNA: the target of molecular interactions between the virus and its host.

- Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.

- A new three-generational family with frontometaphyseal dysplasia, male-to-female transmission, and a previously reported FLNA mutation.


Année 2004

- Association between MSH4 (MutS homologue 4) and the DNA strand-exchange RAD51 and DMC1 proteins during mammalian meiosis.

- Neoadjuvant chemotherapy for symptomatic non operable grade II fibrillary astrocytoma in adults

- Astrocyte infection by HIV-1: mechanisms of restricted virus replication, and role in the pathogenesis of HIV-1-associated dementia.


Année 2003

- Additive activity between the trans-activation response RNA-binding protein, TRBP2, and cyclin T1 on HIV type 1 expression and viral production in murine cells.

- Homologs of MutS and MutL during mammalian meiosis.

- A novel Leishmania infantum nuclear phosphoprotein Lepp12 which stimulates IL1-beta synthesis in THP-1 transfectants.

- The TAR RNA-binding protein, TRBP, stimulates the expression of TAR-containing RNAs in vitro and in vivo independently of its ability to inhibit the dsRNA-dependent kinase PKR.


Année 2002

- The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination.


Année 2001

- Expression of LSLCL, a new C-type lectin, is closely restricted, in bone marrow, to immature neutrophils.

- Organization of the human tarbp2 gene reveals two promoters that are repressed in an astrocytic cell line.

- In vivo involvement of polymorphonuclear neutrophils in Leishmania infantum infection.

- Family of SRY/Sox proteins is involved in the regulation of the mouse Msh4 (MutS Homolog 4) gene expression.

- Two dimerization domains in the trans-activation response RNA-binding protein (TRBP) individually reverse the protein kinase R inhibition of HIV-1 long terminal repeat expression.

- Sustained parasite burden in the spleen of Leishmania infantum-infected BALB/c mice is accompanied by expression of MCP-1 transcripts and lack of protection against challenge.

- Immunisation with DNA encoding Leishmania infantum protein papLe22 decreases the frequency of parasitemic episodes in infected hamsters.


Année 2000

- Characterization of TRBP1 and TRBP2. Stable stem-loop structure at the 5' end of TRBP2 mRNA resembles HIV-1 TAR and is not found in its processed pseudogene.

- MSH4 acts in conjunction with MLH1 during mammalian meiosis.

- A novel Leishmania infantum recombinant antigen which elicits interleukin 10 production by peripheral blood mononuclear cells of patients with visceral leishmaniasis.


Année 1999

- Cloning, mapping, and genomic organization of the LSLCL gene, encoding a new lymphocytic secreted mucin-like protein with a C-type lectin domain: A new model of exon shuffling.

- Alternative splicing of hMSH4: two isoforms in testis and abnormal transcripts in somatic tissues.

- Large-volume leukapheresis procedure for peripheral blood progenitor cell collection in children weighing 15 kg or less: efficacy and safety evaluation.


Année 1998

- Molecular cloning of a new secreted sulfated mucin-like protein with a C-type lectin domain that is expressed in lymphoblastic cells.


Année 1997

- Altered sialylation of alveolar macrophages in HIV-1-infected individuals.

- Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene.

- Cloning and expression of cDNA for a human Gal(beta1-3)GalNAc alpha2,3-sialyltransferase from the CEM T-cell line.


Année 1995

- Muscular involvement in the course of AIDS. Anatomo-clinical study of 17 cases


Année 1994

- Experimental Sertoli cell tumors in the mouse and their progression into a mixed germ cell-sex cord proliferation.


Année 1993

- Transmeiotic differentiation of male germ cells in culture.

- Expression in transgenic mice of the large T antigen of polyomavirus induces Sertoli cell tumours and allows the establishment of differentiated cell lines.


Année 1990

- Branchial dysplasia, mental deficiency, club feet, and inguinal herniae: a report of two further cases associated with paucity of interlobular bile ducts.


Année 1989

- Biochemical and ultrastructural study of two familial cases of Winchester syndrome

- Linkage studies in Emery-Dreifuss muscular dystrophy

- Expressivity of familial forms of Fraser syndrome



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