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Molecular Vision
|
May 20, 2009
Comparative genomic mapping of uncharacterized canine retinal ESTs to identify novel candidate genes for hereditary retinal disorders
B Zangerl, J L Johnson, J Pillardy, et al.
The Journal of Clinical Investigation
|
July 1, 1991
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation
M Garbarz, W T Tse, P G Gallagher, et al.
American Journal of Human Genetics
|
July 1, 1988
Determination of the spectrum of beta-thalassemia genes in Spain by use of dot-blot analysis of amplified beta-globin DNA
S Amselem, V Nunes, M Vidaud, et al.
The EMBO Journal
|
February 1, 1988
Replacement of lys 622 in the ATP binding domain of P100gag-mil abolishes the in vitro autophosphorylation of the protein and the biological properties of the v-mil oncogene of MH2 virus
F Denhez, B Heimann, L d'Auriol, et al.
European Journal of Biochemistry
|
February 15, 1988
Characterization of cDNA clones for human glycophorin A. Use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNA
C Rahuel, J London, L d'Auriol, et al.
Blood
|
April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain
M Garbarz, M C Lecomte, C Féo, et al.
Hepatology (Baltimore, Md.)
|
December 1, 1990
Early and frequent detection of HBxAg and/or anti-HBx in hepatitis B virus infection
L Vitvitski-Trépo, A Kay, C Pichoud, et al.
Genomics
|
June 5, 2004
Detailed four-way comparative mapping and gene order analysis of the canine ctvm locus reveals evolutionary chromosome rearrangements
G Andelfinger, C Hitte, L Etter, et al.
The Journal of Clinical Investigation
|
April 1, 1990
A combination of HLA-DQ beta Asp57-negative and HLA DQ alpha Arg52 confers susceptibility to insulin-dependent diabetes mellitus
I Khalil, L d'Auriol, M Gobet, et al.
Bulletin De L'Academie Nationale De Medecine
|
July 22, 1998
[The importance of the canine model in medical genetics]
F Galibert, C André, A Chéron, et al.
Page
of 22
Search research articles
Search
Showing results (181-190 of 214) with videos related to
Sort By:
Page
of 22
Molecular Vision
|
May 20, 2009
Comparative genomic mapping of uncharacterized canine retinal ESTs to identify novel candidate genes for hereditary retinal disorders
B Zangerl, J L Johnson, J Pillardy, et al.
The Journal of Clinical Investigation
|
July 1, 1991
Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation
M Garbarz, W T Tse, P G Gallagher, et al.
American Journal of Human Genetics
|
July 1, 1988
Determination of the spectrum of beta-thalassemia genes in Spain by use of dot-blot analysis of amplified beta-globin DNA
S Amselem, V Nunes, M Vidaud, et al.
The EMBO Journal
|
February 1, 1988
Replacement of lys 622 in the ATP binding domain of P100gag-mil abolishes the in vitro autophosphorylation of the protein and the biological properties of the v-mil oncogene of MH2 virus
F Denhez, B Heimann, L d'Auriol, et al.
European Journal of Biochemistry
|
February 15, 1988
Characterization of cDNA clones for human glycophorin A. Use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNA
C Rahuel, J London, L d'Auriol, et al.
Blood
|
April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain
M Garbarz, M C Lecomte, C Féo, et al.
Hepatology (Baltimore, Md.)
|
December 1, 1990
Early and frequent detection of HBxAg and/or anti-HBx in hepatitis B virus infection
L Vitvitski-Trépo, A Kay, C Pichoud, et al.
Genomics
|
June 5, 2004
Detailed four-way comparative mapping and gene order analysis of the canine ctvm locus reveals evolutionary chromosome rearrangements
G Andelfinger, C Hitte, L Etter, et al.
The Journal of Clinical Investigation
|
April 1, 1990
A combination of HLA-DQ beta Asp57-negative and HLA DQ alpha Arg52 confers susceptibility to insulin-dependent diabetes mellitus
I Khalil, L d'Auriol, M Gobet, et al.
Bulletin De L'Academie Nationale De Medecine
|
July 22, 1998
[The importance of the canine model in medical genetics]
F Galibert, C André, A Chéron, et al.
Page
of 22