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R Krahe

Showing results (21-30 of 45) with videos related to

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Genomics|July 1, 1995
Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processingR Krahe, T Ashizawa, C Abbruzzese, et al.
Blood|July 11, 2000
Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilinM Kristiansen, M Aminoff, C Jacobsen, et al.
Journal of Neurology|September 23, 2008
High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and GermanyT Suominen, B Schoser, O Raheem, et al.
Genomics|May 15, 1996
Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28G S Iyer, R Krahe, L A Goodwin, et al.
Neurology|November 21, 2008
Premutation allele pool in myotonic dystrophy type 2L L Bachinski, T Czernuszewicz, L S Ramagli, et al.
American Journal of Human Genetics|February 1, 1993
An informative panel of somatic cell hybrids for physical mapping on human chromosome 19qL L Bachinski, R Krahe, B F White, et al.
Genes, Chromosomes & Cancer|December 7, 2000
Aberrant hypermethylation of the major breakpoint cluster region in 17p11.2 in medulloblastomas but not supratentorial PNETsM C Frühwald, M S O'Dorisio, Z Dai, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001
Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogeneticsK Virtaneva, F A Wright, S M Tanner, et al.
Human Molecular Genetics|October 1, 1995
A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeatC A Boucher, S K King, N Carey, et al.
Nature Genetics|May 10, 2000
Mutations in KERA, encoding keratocan, cause cornea planaN S Pellegata, J L Dieguez-Lucena, T Joensuu, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Genomics|July 1, 1995
Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processingR Krahe, T Ashizawa, C Abbruzzese, et al.
Blood|July 11, 2000
Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilinM Kristiansen, M Aminoff, C Jacobsen, et al.
Journal of Neurology|September 23, 2008
High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and GermanyT Suominen, B Schoser, O Raheem, et al.
Genomics|May 15, 1996
Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28G S Iyer, R Krahe, L A Goodwin, et al.
Neurology|November 21, 2008
Premutation allele pool in myotonic dystrophy type 2L L Bachinski, T Czernuszewicz, L S Ramagli, et al.
American Journal of Human Genetics|February 1, 1993
An informative panel of somatic cell hybrids for physical mapping on human chromosome 19qL L Bachinski, R Krahe, B F White, et al.
Genes, Chromosomes & Cancer|December 7, 2000
Aberrant hypermethylation of the major breakpoint cluster region in 17p11.2 in medulloblastomas but not supratentorial PNETsM C Frühwald, M S O'Dorisio, Z Dai, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2001
Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogeneticsK Virtaneva, F A Wright, S M Tanner, et al.
Human Molecular Genetics|October 1, 1995
A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeatC A Boucher, S K King, N Carey, et al.
Nature Genetics|May 10, 2000
Mutations in KERA, encoding keratocan, cause cornea planaN S Pellegata, J L Dieguez-Lucena, T Joensuu, et al.
Pageof 5