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J Sumegi

Showing results (31-40 of 47) with videos related to

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Genomics|December 1, 1991
New strategy for mapping the human genome based on a novel procedure for construction of jumping librariesE R Zabarovsky, F Boldog, R Erlandsson, et al.
American Journal of Human Genetics|January 1, 1995
Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41W J Kimberling, M D Weston, C Möller, et al.
Genomics|June 1, 1993
Alu-PCR approach to isolating NotI-linking clones from the 3p14-p21 region frequently deleted in renal cell carcinomaE R Zabarovsky, V I Kashuba, E S Pokrovskaya, et al.
Blood|October 26, 2000
Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative diseaseJ Sumegi, D Huang, A Lanyi, et al.
FEBS Letters|January 15, 1998
NotI linking/jumping clones of human chromosome 3: mapping of the TFRC, RAB7 and HAUSP genes to regions rearranged in leukemia and deleted in solid tumorsV I Kashuba, R Z Gizatullin, A I Protopopov, et al.
American Journal of Human Genetics|March 23, 2000
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaM D Weston, J D Eudy, S Fujita, et al.
The Journal of Biological Chemistry|July 31, 2001
Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patientsM Morra, M Simarro-Grande, M Martin, et al.
Genomics|February 15, 1997
The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A)P M Kelley, M D Weston, Z Y Chen, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutationsA Trizzino, U zur Stadt, I Ueda, et al.
Cancer Gene Therapy|January 10, 2002
Ex vivo purging by adenoviral p53 gene therapy does not affect NOD-SCID repopulating activity of human CD34+ cellsM Hirai, D LaFace, S Robinson, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Genomics|December 1, 1991
New strategy for mapping the human genome based on a novel procedure for construction of jumping librariesE R Zabarovsky, F Boldog, R Erlandsson, et al.
American Journal of Human Genetics|January 1, 1995
Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41W J Kimberling, M D Weston, C Möller, et al.
Genomics|June 1, 1993
Alu-PCR approach to isolating NotI-linking clones from the 3p14-p21 region frequently deleted in renal cell carcinomaE R Zabarovsky, V I Kashuba, E S Pokrovskaya, et al.
Blood|October 26, 2000
Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative diseaseJ Sumegi, D Huang, A Lanyi, et al.
FEBS Letters|January 15, 1998
NotI linking/jumping clones of human chromosome 3: mapping of the TFRC, RAB7 and HAUSP genes to regions rearranged in leukemia and deleted in solid tumorsV I Kashuba, R Z Gizatullin, A I Protopopov, et al.
American Journal of Human Genetics|March 23, 2000
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaM D Weston, J D Eudy, S Fujita, et al.
The Journal of Biological Chemistry|July 31, 2001
Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patientsM Morra, M Simarro-Grande, M Martin, et al.
Genomics|February 15, 1997
The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A)P M Kelley, M D Weston, Z Y Chen, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutationsA Trizzino, U zur Stadt, I Ueda, et al.
Cancer Gene Therapy|January 10, 2002
Ex vivo purging by adenoviral p53 gene therapy does not affect NOD-SCID repopulating activity of human CD34+ cellsM Hirai, D LaFace, S Robinson, et al.
Pageof 5