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Diabetes
|
March 31, 1998
Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes
C Vigouroux, L Fajas, E Khallouf, et al.
American Journal of Human Genetics
|
November 1, 1995
The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13
L Montermini, F Rodius, L Pianese, et al.
Genetics
|
February 15, 2003
Mosaicism of Solid Gold supports the causality of a noncoding A-to-G transition in the determinism of the callipyge phenotype
Maria Smit, Karin Segers, Laura Garcia Carrascosa, et al.
Genome Research
|
May 5, 2001
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8
C Charlier, K Segers, D Wagenaar, et al.
Complement and Inflammation
|
January 1, 1991
Effect of conditioned media of acute myeloid leukemia blast cells on complement synthesis by cultured human cells of monocyte and hepatocyte origin
G Gyapay, B Schmidt, M Válay, et al.
Nature Genetics
|
October 1, 1993
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
C Ben Hamida, N Doerflinger, S Belal, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2
A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.
American Journal of Human Genetics
|
May 1, 1995
Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families
N Doerflinger, C Linder, K Ouahchi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 11, 2024
A new nonsense pathogenic variant in exon 1 of PHOX2B leads to the diagnosis of congenital central hypoventilation syndrome with intra-familial variability
Morgane Pelleter, Charlène Desaintjean, Romane Gyapay, et al.
Environmental Microbiology
|
May 8, 2008
Discovery and characterization of a new bacterial candidate division by an anaerobic sludge digester metagenomic approach
Sonda Guermazi, Patrick Daegelen, Catherine Dauga, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 92) with videos related to
Sort By:
Page
of 10
Diabetes
|
March 31, 1998
Human peroxisome proliferator-activated receptor-gamma2: genetic mapping, identification of a variant in the coding sequence, and exclusion as the gene responsible for lipoatrophic diabetes
C Vigouroux, L Fajas, E Khallouf, et al.
American Journal of Human Genetics
|
November 1, 1995
The Friedreich ataxia critical region spans a 150-kb interval on chromosome 9q13
L Montermini, F Rodius, L Pianese, et al.
Genetics
|
February 15, 2003
Mosaicism of Solid Gold supports the causality of a noncoding A-to-G transition in the determinism of the callipyge phenotype
Maria Smit, Karin Segers, Laura Garcia Carrascosa, et al.
Genome Research
|
May 5, 2001
Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8
C Charlier, K Segers, D Wagenaar, et al.
Complement and Inflammation
|
January 1, 1991
Effect of conditioned media of acute myeloid leukemia blast cells on complement synthesis by cultured human cells of monocyte and hepatocyte origin
G Gyapay, B Schmidt, M Válay, et al.
Nature Genetics
|
October 1, 1993
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
C Ben Hamida, N Doerflinger, S Belal, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2
A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.
American Journal of Human Genetics
|
May 1, 1995
Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families
N Doerflinger, C Linder, K Ouahchi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
September 11, 2024
A new nonsense pathogenic variant in exon 1 of PHOX2B leads to the diagnosis of congenital central hypoventilation syndrome with intra-familial variability
Morgane Pelleter, Charlène Desaintjean, Romane Gyapay, et al.
Environmental Microbiology
|
May 8, 2008
Discovery and characterization of a new bacterial candidate division by an anaerobic sludge digester metagenomic approach
Sonda Guermazi, Patrick Daegelen, Catherine Dauga, et al.
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of 10