Author details

Full Name

Colin F Fletcher

Affiliation

ORCID

Career Start Year

1984

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
30854487	Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts.	Commun Biol	2019
22968824	The mammalian gene function resource: the International Knockout Mouse Consortium.	Mamm Genome	2012
19635938	The role of MITF phosphorylation sites during coat color and eye development in mice analyzed by bacterial artificial chromosome transgene rescue.	Genetics	2009
18597946	Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.	Neuroscience	2008
16890369	Pain sensitivity in mice lacking the Ca(v)2.1alpha1 subunit of P/Q-type Ca2+ channels.	Neuroscience	2006
16683036	Transcript annotation in FANTOM3: mouse gene catalog based on physical cDNAs.	PLoS Genet	2006
16141072	The transcriptional landscape of the mammalian genome.	Science	2005
15000527	In vivo analysis of voltage-dependent calcium channels.	Journal of Bioenergetics and Biomembranes	2003
12509841	Do calcium channel autoantibodies cause cerebellar ataxia with Lambert-Eaton syndrome?	Annals of Neurology	2003
12612341	Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse.	Proc Natl Acad Sci U S A	2003
14504232	Transposon mutagenesis of the mouse germline.	Genetics	2003
12819138	Analysis of the mouse transcriptome for genes involved in the function of the nervous system.	Genome Res	2003
12466851	Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.	Nature	2002
11904379	Mammalian germ-line transgenesis by transposition.	Proc Natl Acad Sci U S A	2002
12235360	Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.	Proceedings of the National Academy of Sciences of the United States of America	2002
12368914	Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease.	Nature Genetics	2002
11344116	Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.	FASEB J	2001
11504925	Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice.	Proceedings of the National Academy of Sciences of the United States of America	2001
11217851	Functional annotation of a full-length mouse cDNA collection.	Nature	2001
11233449	Sequence interpretation. Functional annotation of mouse genome sequences.	Science	2001
11102459	The status of voltage-dependent calcium channels in alpha 1E knock-out mice.	Journal of Neuroscience	2000
11133404	Calcium channels: critical targets of toxicants and diseases.	Environ Health Perspect	2000
10908603	Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)).	Journal of Neuroscience	2000
10469844	Ataxic mouse mutants and molecular mechanisms of absence epilepsy.	Human Molecular Genetics	1999
10087299	Exon structure of the nuclear factor I DNA-binding domain from C. elegans to mammals.	Mammalian Genome	1999
10322048	Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalami.	J Neurophysiol	1999
10321731	Mrvi1, a common MRV integration site in BXH2 myeloid leukemias, encodes a protein with homology to a lymphoid-restricted membrane protein Jaw1.	Oncogene	1999
9758334	Genetic analysis of voltage-dependent calcium channels.	Journal of Bioenergetics and Biomembranes	1998
9521885	Assignment of the mouse Pde7A gene to the proximal region of chromosome 3 and of the human PDE7A gene to chromosome 8q13.	Genomics	1998
9344654	Mouse chromosomal locations of nine genes encoding homologs of human paraneoplastic neurologic disorder antigens.	Genomics	1997
9441664	The cut-homeodomain transcriptional activator HNF-6 is coexpressed with its target gene HNF-3 beta in the developing murine liver and pancreas.	Developmental Biology	1997
9368758	Long-term monitoring of circadian rhythms in c-fos gene expression from suprachiasmatic nucleus cultures.	Curr Biol	1997
9143490	Chromosomal mapping of five highly conserved murine homologues of the Drosophila RING finger gene seven-in-absentia.	Genomics	1997
8812055	Expression patterns of two murine homologs of Drosophila single-minded suggest possible roles in embryonic patterning and in the pathogenesis of Down syndrome.	Mol Cell Neurosci	1996
8875433	Expression patterns of two murine homologs of Drosophila single-minded suggest possible roles in embryonic patterning and in the pathogenesis of Down syndrome..	Molecular and Cellular Neurosciences	1996
8929530	Absence epilepsy in tottering mutant mice is associated with calcium channel defects.	Cell	1996
8798505	Genesis, a winged helix transcriptional repressor with expression restricted to embryonic stem cells.	J Biol Chem	1996
7789972	Murine chromosomal location of eight members of the hepatocyte nuclear factor 3/fork head winged helix family of transcription factors.	Genomics	1995
8026336	Maintenance of Wnt-3 expression in Purkinje cells of the mouse cerebellum depends on interactions with granule cells.	Development (Cambridge)	1994
7877445	Genomic structure and mapping of precerebellin and a precerebellin-related gene.	Molecular Brain Research	1994
1783403	Characterization and functional expression of a cDNA encoding egasyn (esterase-22): the endoplasmic reticulum-targeting protein of beta-glucuronidase.	Genomics	1991
1672287	Genetic mapping of the lurcher locus on mouse chromosome 6 using an intersubspecific backcross.	Genomics	1991
2037298	A multilocus linkage map of mouse chromosome 8.	Genomics	1991
2037292	Genetic mapping of meander tail, a mouse mutation affecting cerebellar development.	Genomics	1991
2349228	Meander tail reveals a discrete developmental unit in the mouse cerebellum.	Proc Natl Acad Sci U S A	1990
3413485	Transcription factor OTF-1 is functionally identical to the DNA replication factor NF-III.	Science	1988
3677172	Purification and characterization of OTF-1, a transcription factor regulating cell cycle expression of a human histone H2b gene.	Cell	1987
6326094	Isolation of a collagenase cDNA clone and measurement of changing collagenase mRNA levels during induction in rabbit synovial fibroblasts.	Proceedings of the National Academy of Sciences of the United States of America	1984