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D E Jenne

Showing results (31-40 of 42) with videos related to

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Blood|July 1, 1993
Human megakaryocytes express clusterin and package it without apolipoprotein A-1 into alpha-granulesJ Tschopp, D E Jenne, S Hertig, et al.
Genomics|June 14, 2000
A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletionsD E Jenne, S Tinschert, E Stegmann, et al.
Human Genetics|February 1, 1997
The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regionsH Kehrer-Sawatzki, J Häussler, W Krone, et al.
Nature Genetics|January 13, 1998
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinaseD E Jenne, H Reimann, J Nezu, et al.
Immunity|May 24, 2001
Migratory activity and functional changes of green fluorescent effector cells before and during experimental autoimmune encephalomyelitisA Flügel, T Berkowicz, T Ritter, et al.
American Journal of Human Genetics|July 17, 2004
High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 geneH Kehrer-Sawatzki, L Kluwe, C Sandig, et al.
Genomics|June 6, 1998
Structure of the human paralemmin gene (PALM), mapping to human chromosome 19p13.3 and mouse chromosome 10, and exclusion of coding mutations in grizzled, mocha, jittery, and hesitant miceB Burwinkel, G Miglierini, D E Jenne, et al.
Genes, Chromosomes & Cancer|July 9, 1999
Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patientsW Friedl, R Kruse, S Uhlhaas, et al.
Nature Genetics|February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninE S Moreira, T J Wiltshire, G Faulkner, et al.
Genome Research|September 14, 2000
Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpointsR Puttagunta, L A Gordon, G E Meyer, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Blood|July 1, 1993
Human megakaryocytes express clusterin and package it without apolipoprotein A-1 into alpha-granulesJ Tschopp, D E Jenne, S Hertig, et al.
Genomics|June 14, 2000
A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletionsD E Jenne, S Tinschert, E Stegmann, et al.
Human Genetics|February 1, 1997
The second case of a t(17;22) in a family with neurofibromatosis type 1: sequence analysis of the breakpoint regionsH Kehrer-Sawatzki, J Häussler, W Krone, et al.
Nature Genetics|January 13, 1998
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinaseD E Jenne, H Reimann, J Nezu, et al.
Immunity|May 24, 2001
Migratory activity and functional changes of green fluorescent effector cells before and during experimental autoimmune encephalomyelitisA Flügel, T Berkowicz, T Ritter, et al.
American Journal of Human Genetics|July 17, 2004
High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 geneH Kehrer-Sawatzki, L Kluwe, C Sandig, et al.
Genomics|June 6, 1998
Structure of the human paralemmin gene (PALM), mapping to human chromosome 19p13.3 and mouse chromosome 10, and exclusion of coding mutations in grizzled, mocha, jittery, and hesitant miceB Burwinkel, G Miglierini, D E Jenne, et al.
Genes, Chromosomes & Cancer|July 9, 1999
Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patientsW Friedl, R Kruse, S Uhlhaas, et al.
Nature Genetics|February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninE S Moreira, T J Wiltshire, G Faulkner, et al.
Genome Research|September 14, 2000
Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpointsR Puttagunta, L A Gordon, G E Meyer, et al.
Pageof 5