I Aksentijevich - JoVE Visualize

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Human Genetics|July 1, 1993

Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error?I Aksentijevich, L Gruberg, E Pras, et al.

American Journal of Human Genetics|June 1, 1995

Mutations in the SLC3A1 transporter gene in cystinuriaE Pras, N Raben, E Golomb, et al.

Scandinavian Journal of Rheumatology|September 2, 2005

Analysis of CARD15/NOD2 haplotypes fails to identify common variants associated with rheumatoid arthritis susceptibilityA Addo, J Le, W Li, et al.

The New England Journal of Medicine|June 14, 1992

Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16E Pras, I Aksentijevich, L Gruberg, et al.

Nature Genetics|April 1, 1994

Localization of a gene causing cystinuria to chromosome 2pE Pras, N Arber, I Aksentijevich, et al.

European Journal of Human Genetics : EJHG|February 15, 2001

Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Dutch family: evidence for a TNFRSF1A mutation with reduced penetranceE Aganna, I Aksentijevich, G A Hitman, et al.

American Journal of Human Genetics|August 1, 1993

Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studiesI Aksentijevich, E Pras, L Gruberg, et al.

American Journal of Human Genetics|September 1, 1993

Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysisI Aksentijevich, E Pras, L Gruberg, et al.

Clinical Genetics|January 8, 2008

Familial Mediterranean Fever in Crete: a genetic and structural biological approach in a population of 'intermediate risk'E Fragouli, E Eliopoulos, E Petraki, et al.

Blood|February 15, 1992

Transplantation of bone marrow cells from transgenic mice expressing the human MDR1 gene results in long-term protection against the myelosuppressive effect of chemotherapy in miceG H Mickisch, I Aksentijevich, P V Schoenlein, et al.

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Showing results (31-40 of 56) with videos related to

Sort By:

Pageof 6

Human Genetics|July 1, 1993

Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error?I Aksentijevich, L Gruberg, E Pras, et al.

American Journal of Human Genetics|June 1, 1995

Mutations in the SLC3A1 transporter gene in cystinuriaE Pras, N Raben, E Golomb, et al.

Scandinavian Journal of Rheumatology|September 2, 2005

Analysis of CARD15/NOD2 haplotypes fails to identify common variants associated with rheumatoid arthritis susceptibilityA Addo, J Le, W Li, et al.

The New England Journal of Medicine|June 14, 1992

Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16E Pras, I Aksentijevich, L Gruberg, et al.

Nature Genetics|April 1, 1994

Localization of a gene causing cystinuria to chromosome 2pE Pras, N Arber, I Aksentijevich, et al.

European Journal of Human Genetics : EJHG|February 15, 2001

Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Dutch family: evidence for a TNFRSF1A mutation with reduced penetranceE Aganna, I Aksentijevich, G A Hitman, et al.

American Journal of Human Genetics|August 1, 1993

Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studiesI Aksentijevich, E Pras, L Gruberg, et al.

American Journal of Human Genetics|September 1, 1993

Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysisI Aksentijevich, E Pras, L Gruberg, et al.

Clinical Genetics|January 8, 2008

Familial Mediterranean Fever in Crete: a genetic and structural biological approach in a population of 'intermediate risk'E Fragouli, E Eliopoulos, E Petraki, et al.

Blood|February 15, 1992

Transplantation of bone marrow cells from transgenic mice expressing the human MDR1 gene results in long-term protection against the myelosuppressive effect of chemotherapy in miceG H Mickisch, I Aksentijevich, P V Schoenlein, et al.

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