Search Results - "Guenet, L"
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The stromal gene encoding the CD274 antigen as a genetic modifier controlling survival of mice with γ-radiation-induced T-cell lymphoblastic lymphomas
Published in Oncogene (23-09-2010)“…Using an inter-specific subcongenic strain, Nested Recombinant Haplotype 3 (NRH3), generated between two mouse strains showing extreme differences in…”
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Susceptibility to Experimental Cerebral Malaria Induced by Plasmodium berghei ANKA in Inbred Mouse Strains Recently Derived from Wild Stock
Published in Infection and Immunity (01-04-2002)“…Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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3
Sphingomyelin Degradation is a Key Factor in Dentin and Bone Mineralization: Lessons from the fro/fro Mouse
Published in Journal of dental research (01-01-2008)Get full text
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4
Rat Gene Mapping Using PCR-Analyzed Microsatellites
Published in Genetics (Austin) (01-07-1992)“…One hundred and seventy-four rat loci which contain short tandem repeat sequences were extracted from the GenBank or EMBL data bases and used to define primers…”
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5
Comparison of polyclonal and monoclonal antibody based free light chain assays taking account of renal function
Published in Clinical lymphoma, myeloma and leukemia (01-09-2015)Get full text
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Heavy/light chain specific immunoglobulin ratios provides no additional information than serum proteins electrophoresis and immunofixation for the diagnosis and the follow-up of intact immunoglobulin multiple myeloma patients
Published in Pathologie biologie (Paris) (01-09-2015)“…Serum protein electrophoresis (SPE) and immunofixation electrophoresis (IFE) are used for diagnosis and follow-up of patients with intact immunoglobulin…”
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Several classical mouse inbred strains, including DBA/2, NOD/Lt, FVB/N, and SJL/J, carry a putative loss-of-function allele of Gpr84
Published in The Journal of heredity (01-07-2013)“…G protein-coupled receptor 84 (GPR84) is a 7-transmembrane protein expressed on myeloid cells that can bind to medium-chain free fatty acids in vitro. Here, we…”
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Pax: a murine multigene family of paired box-containing genes
Published in Genomics (San Diego, Calif.) (01-10-1991)“…A murine multigene family has been identified that shares a conserved sequence motif, the paired box, with developmental control and tissue-specific genes of…”
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Sequence interpretation. Functional annotation of mouse genome sequences
Published in Science (American Association for the Advancement of Science) (16-02-2001)Get full text
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A Single Base Deletion in the Tfm Androgen Receptor Gene Creates a Short-Lived Messenger RNA that Directs Internal Translation Initiation
Published in Proceedings of the National Academy of Sciences - PNAS (01-10-1991)“…Testosterone-resistant male mice hemizygous for the X-chromosome-linked mutant gene Tfm express detectable but severely reduced levels of androgen receptor…”
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Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1 : structure, function, regulation of expression and chromosomal localization
Published in Biochemical journal (15-09-1994)“…We have isolated cDNA clones encoding an inositol 1,4,5-trisphosphate receptor type 1 (InsP3R1) from human uteri and a leukaemic cell line, HL-60…”
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A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestine
Published in Genes & development (01-12-1988)“…A mouse gene, Cdx-1, was isolated from an embryonic cDNA library using a Drosophila caudal gene probe. The deduced amino acid sequence of Cdx-1 contains…”
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13
The human gene for alkaptonuria (AKU) maps to chromosome 3q
Published in Genomics (San Diego, Calif.) (01-01-1994)“…Alkaptonuria (AKU; McKusick no. 203500) is a rare autosomal recessive disorder caused by the lack of homogentisic acid oxidase activity. Patients excrete large…”
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Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders
Published in Genetica (01-09-2004)“…With the completion of the first draft of the human genome sequence, the next major challenge is assigning function to genes. One approach is genome-wide…”
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cDNA Isolation, Expression, and Chromosomal Localization of the Mouse Survival Motor Neuron Gene (Smn)
Published in Genomics (San Diego, Calif.) (15-02-1997)“…Spinal muscular atrophy (SMA) is a frequent autosomal recessive disease in human characterized by degeneration of motor neurons of the spinal cord. The genomic…”
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16
Un liquide céphalorachidien coloré
Published in La revue de medecine interne (01-03-2011)Get full text
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An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrids
Published in Nature genetics (01-04-1996)“…Interspecific hybridization between closely related species is commonly associated with decreased fertility or viability of F sub(1) hybrids. Thus, in mouse…”
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Expression of the L14 lectin during mouse embryogenesis suggests multiple roles during pre- and post-implantation development
Published in Development (Cambridge) (01-05-1992)“…A cDNA encoding L14, the lactose-binding, soluble lectin of relative molecular mass 14 Ã 10(3), has been isolated in a differential screen designed to…”
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Minisatellite Linkage Maps in the Mouse by Cross-Hybridization with Human Probes Containing Tandem Repeats
Published in Proceedings of the National Academy of Sciences - PNAS (01-06-1990)“…Tests of 29 human variable number of tandem repeat probes in inbred mouse lines showed that 80% (23/29) cross-hybridize, and 48% (14/29) produce multiple band,…”
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Structure and chromosomal assignment of the mouse fra-1 gene, and its exclusion as a candidate gene for oc (osteosclerosis)
Published in Oncogene (04-09-1997)“…We have determined the genomic structure of the mouse fra-1 gene, which consists of four exons and three introns at positions also found in the other members…”
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