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http://hub.abes.fr/springer/periodical/335/1991/volume_1/issue_1/B8CA678C354B66D6E053120B220A2E8F/authorship/1
http://hub.abes.fr/springer/periodical/335/1992/volume_3/issue_8/B8CA678C35A266D6E053120B220A2E8F/authorship/3
http://hub.abes.fr/springer/periodical/335/1993/volume_4/issue_6/B8CA678C362D66D6E053120B220A2E8F/authorship/5
http://hub.abes.fr/springer/periodical/335/1991/volume_1/issue_3/B8CA678C352C66D6E053120B220A2E8F/authorship/3
http://hub.abes.fr/springer/periodical/335/1996/volume_7/issue_1/B8CA678C387166D6E053120B220A2E8F/authorship/1
http://hub.abes.fr/springer/periodical/335/1992/volume_3/issue_4/B8CA678C358566D6E053120B220A2E8F/authorship/4
http://hub.abes.fr/springer/periodical/335/1995/volume_6/issue_11/B8CA678C36B666D6E053120B220A2E8F/authorship/7
http://hub.abes.fr/springer/periodical/335/1993/volume_4/issue_9/B8CA678C35E566D6E053120B220A2E8F/authorship/5
http://hub.abes.fr/springer/periodical/335/1991/volume_1/issue_3/B8CA678C353066D6E053120B220A2E8F/authorship/4
http://hub.abes.fr/springer/periodical/335/1992/volume_2/issue_2/B8CAF61807C17BDEE053120B220A0467/authorship/4
http://hub.abes.fr/springer/periodical/335/1992/volume_3/issue_2/B8CA678C35D966D6E053120B220A2E8F/authorship/4
http://hub.abes.fr/springer/periodical/335/1993/volume_4/issue_7/B8CA678C365F66D6E053120B220A2E8F/authorship/4
http://hub.abes.fr/springer/periodical/335/1996/volume_7/issue_4/B8CA678C380766D6E053120B220A2E8F/authorship/6
http://hub.abes.fr/springer/periodical/335/1992/volume_2/issue_4/B8CAF61807B17BDEE053120B220A0467/authorship/5
http://hub.abes.fr/springer/periodical/335/1992/volume_3/issue_11/B8CA678C356766D6E053120B220A2E8F/authorship/3
http://hub.abes.fr/springer/periodical/335/1993/volume_4/issue_10/B8CA678C360E66D6E053120B220A2E8F/authorship/8
http://hub.abes.fr/springer/periodical/335/1994/volume_5/issue_11/B8CA678C38F166D6E053120B220A2E8F/authorship/4
http://hub.abes.fr/springer/periodical/251/1992/volume_35/issue_5/B93AB2785ED41B66E053120B220ADD35/authorship/5
http://hub.abes.fr/springer/periodical/335/1992/volume_3/issue_1/B8CA678C35C266D6E053120B220A2E8F/authorship/1
http://hub.abes.fr/springer/periodical/335/1993/volume_4/issue_1/B8CA678C366B66D6E053120B220A2E8F/authorship/1
http://hub.abes.fr/springer/periodical/335/1996/volume_7/issue_11/B8CA678C37B666D6E053120B220A2E8F/authorship/2
http://hub.abes.fr/springer/periodical/335/1991/volume_1/issue_4/B8CA678C352A66D6E053120B220A2E8F/authorship/3
http://hub.abes.fr/springer/periodical/335/1992/volume_3/issue_3/B8CA678C359866D6E053120B220A2E8F/authorship/2
http://hub.abes.fr/springer/periodical/335/1995/volume_6/issue_11/B8CA678C36C366D6E053120B220A2E8F/authorship/1
http://hub.abes.fr/springer/periodical/335/1996/volume_7/issue_12/B8CA678C38AE66D6E053120B220A2E8F/authorship/4
http://hub.abes.fr/springer/periodical/335/1994/volume_5/issue_6/B8CA678C392A66D6E053120B220A2E8F/authorship/5
http://hub.abes.fr/springer/periodical/335/1996/volume_7/issue_1/B8CA678C387766D6E053120B220A2E8F/authorship/3
http://hub.abes.fr/springer/periodical/335/1995/volume_6/issue_5/B8CA678C36D766D6E053120B220A2E8F/authorship/1
http://hub.abes.fr/springer/periodical/335/1996/volume_7/issue_10/B8CA678C37E366D6E053120B220A2E8F/authorship/7
http://hub.abes.fr/springer/periodical/335/1994/volume_5/issue_7/B8CA678C396266D6E053120B220A2E8F/authorship/7
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http://hub.abes.fr/springer/periodical/335/1991/volume_1/issue_1/B8CA678C353766D6E053120B220A2E8F/authorship/3
http://hub.abes.fr/springer/periodical/335/1993/volume_4/issue_1/B8CA678C364E66D6E053120B220A2E8F/authorship/4
http://hub.abes.fr/springer/periodical/431/1992/volume_151/issue_2/B90485A6974A52DAE053120B220AAC7B/authorship/5
http://hub.abes.fr/springer/periodical/439/1990/volume_85/issue_3/B9279D37EEC45861E053120B220A3025/authorship/2
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The gene coding for the immunoglobulin heavy chain binding protein BiP (Hsce-70) maps to mouse Chromosome 2
Gtl2lacZ, an insertional mutation on mouse Chromosome 12 with parental origin-dependent phenotype
A high-resolution genetic map of mouse Chromosome 15 encompassing the Dominant megacolon (Dom) locus
Two-dimensional gel analysis of complex DNA families: Methodology and apparatus
The serotonin 5-HT1B receptor subtype (Htr1b) gene maps to mouse Chromosome 9
PCR-analyzed microsatellites: Data concerning laboratory and wild-derived mouse inbred strains
Polymorphisms revealed by PCR with single, short-sized, arbitrary primers are reliable markers for mouse and rat gene mapping
DNA segments mapped by reciprocal use of microsatellite primers between mouse and rat
The gene coding for the kidney androgen-regulated protein (Kap), maps between the Gapd and Kras-2 genes on mouse Chromosome 6
The locus Om, responsible for the DDK syndrome, maps close to Sigje on mouse Chromosome 11
Mouse chromosome 19
A set of anonymous DNA clones as markers for mouse gene mapping
Mouse Chromosome 19
Molecular map of Chromosome 19 including three genes affecting bleeding time: ep, ru, and bm
The mouse gene (Mobp) encoding myelin-associated oligodendrocytic basic protein maps to distal Chromosome 9
The gene encoding sarcoplasmic reticulum calcium ATPase-1 (Atp2al) maps to distal mouse Chromosome 7
Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus
The gene coding for variant hepatic nuclear factor 1 (Tcf-2), maps between the Edp-1 and Erba genes on mouse Chromosome 11
The genes coding for alpha and beta catenin (Catna1 and Catnb) and Plakoglobin (Jup) map to mouse Chromosomes 18, 9, and 11, respectively
Re-localization of Actsk-1 to mouse Chromosome 8, a new region of homology with human Chromosome 1
Rbt (rabo torcido), a new mouse skeletal mutation involved in anteroposterior patterning of the axial skeleton, maps close to the ts (tail-short) locus and distal to the sox9 locus on chromosome 11
The mouse homolog to the ras-related yeast gene YPT1 maps on Chromosome 11 close to the wobbler (wr) locus
The gene coding for the α1 subunit of the skeletal dihydropyridine receptor (Cchl1a3=mdg) maps to mouse Chromosome 1 and human 1q32
The cDNA sequence of mouse uroporphyrinogen III synthase and assignment to mouse Chromosome 7
Ascorbic acid and alkaptonuria
Mapping of the genes encoding tum- transplantation antigens P91A, P35B, and P198
Tg (9 HSA-MYC), a homozygous lethal insertion in the mouse
Msx1 is close but not allelic to either Hm or Hx on mouse Chromosome 5
The gene encoding the thrombin receptor (Cf2r) maps to mouse Chromosome 13
Fine genetic mapping of the proximal part of mouse Chromosome 2 excludes Pax-8 as a candidate gene for Danforth's short tail (Sd)
The mouse goosecoïd gene (Gsc) maps to the telomeric part of mouse Chromosome 12
Chromosomal localization of two cell surface-associated molecules of potential importance in development: Midkine (Mdk) and basigin (Bsg)
Mouse chromosome 19
Meiotic mapping of murine chromosome 17: The string of loci around l(17)-2Pas
Cardiac and skeletal muscle troponin I isoforms are encoded by a dispersed gene family on mouse Chromosomes 1 and 7
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