L Naftalin|C F Fletcher - JoVE Visualize

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Proceedings of the National Academy of Sciences of the United States of America|April 1, 1984

Isolation of a collagenase cDNA clone and measurement of changing collagenase mRNA levels during induction in rabbit synovial fibroblastsR H Gross, L A Sheldon, C F Fletcher, et al.

Brain Research. Molecular Brain Research|November 1, 1994

Genomic structure and mapping of precerebellin and a precerebellin-related geneB Kavety, N A Jenkins, C F Fletcher, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 24, 1999

Exon structure of the nuclear factor I DNA-binding domain from C. elegans to mammalsC F Fletcher, N A Jenkins, N G Copeland, et al.

Journal of Neurophysiology|May 13, 1999

Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalamiS J Caddick, C Wang, C F Fletcher, et al.

Neuroscience|August 8, 2006

Pain sensitivity in mice lacking the Ca(v)2.1alpha1 subunit of P/Q-type Ca2+ channelsS Luvisetto, S Marinelli, M S Panasiti, et al.

Developmental Biology|January 27, 1998

The cut-homeodomain transcriptional activator HNF-6 is coexpressed with its target gene HNF-3 beta in the developing murine liver and pancreasF Rausa, U Samadani, H Ye, et al.

Genomics|April 15, 1997

Chromosomal mapping of five highly conserved murine homologues of the Drosophila RING finger gene seven-in-absentiaA J Holloway, N G Della, C F Fletcher, et al.

Genomics|November 5, 1997

Mouse chromosomal locations of nine genes encoding homologs of human paraneoplastic neurologic disorder antigensC F Fletcher, H J Okano, D J Gilbert, et al.

Oncogene|May 13, 1999

Mrvi1, a common MRV integration site in BXH2 myeloid leukemias, encodes a protein with homology to a lymphoid-restricted membrane protein Jaw1J D Shaughnessy, D A Largaespada, E Tian, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 16, 2001

Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden miceL E Matesic, R Yip, A E Reuss, et al.

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Showing results (11-20 of 28) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|April 1, 1984

Isolation of a collagenase cDNA clone and measurement of changing collagenase mRNA levels during induction in rabbit synovial fibroblastsR H Gross, L A Sheldon, C F Fletcher, et al.

Brain Research. Molecular Brain Research|November 1, 1994

Genomic structure and mapping of precerebellin and a precerebellin-related geneB Kavety, N A Jenkins, C F Fletcher, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 24, 1999

Exon structure of the nuclear factor I DNA-binding domain from C. elegans to mammalsC F Fletcher, N A Jenkins, N G Copeland, et al.

Journal of Neurophysiology|May 13, 1999

Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalamiS J Caddick, C Wang, C F Fletcher, et al.

Neuroscience|August 8, 2006

Pain sensitivity in mice lacking the Ca(v)2.1alpha1 subunit of P/Q-type Ca2+ channelsS Luvisetto, S Marinelli, M S Panasiti, et al.

Developmental Biology|January 27, 1998

The cut-homeodomain transcriptional activator HNF-6 is coexpressed with its target gene HNF-3 beta in the developing murine liver and pancreasF Rausa, U Samadani, H Ye, et al.

Genomics|April 15, 1997

Chromosomal mapping of five highly conserved murine homologues of the Drosophila RING finger gene seven-in-absentiaA J Holloway, N G Della, C F Fletcher, et al.

Genomics|November 5, 1997

Mouse chromosomal locations of nine genes encoding homologs of human paraneoplastic neurologic disorder antigensC F Fletcher, H J Okano, D J Gilbert, et al.

Oncogene|May 13, 1999

Mrvi1, a common MRV integration site in BXH2 myeloid leukemias, encodes a protein with homology to a lymphoid-restricted membrane protein Jaw1J D Shaughnessy, D A Largaespada, E Tian, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 16, 2001

Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden miceL E Matesic, R Yip, A E Reuss, et al.

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