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Items: 36

1.

Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.

Miki T, Zwingman TA, Wakamori M, Lutz CM, Cook SA, Hosford DA, Herrup K, Fletcher CF, Mori Y, Frankel WN, Letts VA.

Neuroscience. 2008 Jul 31;155(1):31-44. doi: 10.1016/j.neuroscience.2008.05.028. Epub 2008 Jul 1.

2.

Pain sensitivity in mice lacking the Ca(v)2.1alpha1 subunit of P/Q-type Ca2+ channels.

Luvisetto S, Marinelli S, Panasiti MS, D'Amato FR, Fletcher CF, Pavone F, Pietrobon D.

Neuroscience. 2006 Oct 27;142(3):823-32. Epub 2006 Aug 4.

PMID:
16890369
3.

Transcript annotation in FANTOM3: mouse gene catalog based on physical cDNAs.

Maeda N, Kasukawa T, Oyama R, Gough J, Frith M, Engström PG, Lenhard B, Aturaliya RN, Batalov S, Beisel KW, Bult CJ, Fletcher CF, Forrest AR, Furuno M, Hill D, Itoh M, Kanamori-Katayama M, Katayama S, Katoh M, Kawashima T, Quackenbush J, Ravasi T, Ring BZ, Shibata K, Sugiura K, Takenaka Y, Teasdale RD, Wells CA, Zhu Y, Kai C, Kawai J, Hume DA, Carninci P, Hayashizaki Y.

PLoS Genet. 2006 Apr;2(4):e62.

4.

The transcriptional landscape of the mammalian genome.

Carninci P, Kasukawa T, Katayama S, Gough J, Frith MC, Maeda N, Oyama R, Ravasi T, Lenhard B, Wells C, Kodzius R, Shimokawa K, Bajic VB, Brenner SE, Batalov S, Forrest AR, Zavolan M, Davis MJ, Wilming LG, Aidinis V, Allen JE, Ambesi-Impiombato A, Apweiler R, Aturaliya RN, Bailey TL, Bansal M, Baxter L, Beisel KW, Bersano T, Bono H, Chalk AM, Chiu KP, Choudhary V, Christoffels A, Clutterbuck DR, Crowe ML, Dalla E, Dalrymple BP, de Bono B, Della Gatta G, di Bernardo D, Down T, Engstrom P, Fagiolini M, Faulkner G, Fletcher CF, Fukushima T, Furuno M, Futaki S, Gariboldi M, Georgii-Hemming P, Gingeras TR, Gojobori T, Green RE, Gustincich S, Harbers M, Hayashi Y, Hensch TK, Hirokawa N, Hill D, Huminiecki L, Iacono M, Ikeo K, Iwama A, Ishikawa T, Jakt M, Kanapin A, Katoh M, Kawasawa Y, Kelso J, Kitamura H, Kitano H, Kollias G, Krishnan SP, Kruger A, Kummerfeld SK, Kurochkin IV, Lareau LF, Lazarevic D, Lipovich L, Liu J, Liuni S, McWilliam S, Madan Babu M, Madera M, Marchionni L, Matsuda H, Matsuzawa S, Miki H, Mignone F, Miyake S, Morris K, Mottagui-Tabar S, Mulder N, Nakano N, Nakauchi H, Ng P, Nilsson R, Nishiguchi S, Nishikawa S, Nori F, Ohara O, Okazaki Y, Orlando V, Pang KC, Pavan WJ, Pavesi G, Pesole G, Petrovsky N, Piazza S, Reed J, Reid JF, Ring BZ, Ringwald M, Rost B, Ruan Y, Salzberg SL, Sandelin A, Schneider C, Schönbach C, Sekiguchi K, Semple CA, Seno S, Sessa L, Sheng Y, Shibata Y, Shimada H, Shimada K, Silva D, Sinclair B, Sperling S, Stupka E, Sugiura K, Sultana R, Takenaka Y, Taki K, Tammoja K, Tan SL, Tang S, Taylor MS, Tegner J, Teichmann SA, Ueda HR, van Nimwegen E, Verardo R, Wei CL, Yagi K, Yamanishi H, Zabarovsky E, Zhu S, Zimmer A, Hide W, Bult C, Grimmond SM, Teasdale RD, Liu ET, Brusic V, Quackenbush J, Wahlestedt C, Mattick JS, Hume DA, Kai C, Sasaki D, Tomaru Y, Fukuda S, Kanamori-Katayama M, Suzuki M, Aoki J, Arakawa T, Iida J, Imamura K, Itoh M, Kato T, Kawaji H, Kawagashira N, Kawashima T, Kojima M, Kondo S, Konno H, Nakano K, Ninomiya N, Nishio T, Okada M, Plessy C, Shibata K, Shiraki T, Suzuki S, Tagami M, Waki K, Watahiki A, Okamura-Oho Y, Suzuki H, Kawai J, Hayashizaki Y; FANTOM Consortium; RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group).

Science. 2005 Sep 2;309(5740):1559-63. Erratum in: Science. 2006 Mar 24;311(5768):1713.

5.

In vivo analysis of voltage-dependent calcium channels.

Liu L, Zwingman TA, Fletcher CF.

J Bioenerg Biomembr. 2003 Dec;35(6):671-85. Review.

PMID:
15000527
6.

Transposon mutagenesis of the mouse germline.

Carlson CM, Dupuy AJ, Fritz S, Roberg-Perez KJ, Fletcher CF, Largaespada DA.

Genetics. 2003 Sep;165(1):243-56.

7.

Analysis of the mouse transcriptome for genes involved in the function of the nervous system.

Gustincich S, Batalov S, Beisel KW, Bono H, Carninci P, Fletcher CF, Grimmond S, Hirokawa N, Jarvis ED, Jegla T, Kawasawa Y, LeMieux J, Miki H, Raviola E, Teasdale RD, Tominaga N, Yagi K, Zimmer A, Hayashizaki Y, Okazaki Y; RIKEN GER Group; GSL Members.

Genome Res. 2003 Jun;13(6B):1395-401.

8.

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse.

Wiltshire T, Pletcher MT, Batalov S, Barnes SW, Tarantino LM, Cooke MP, Wu H, Smylie K, Santrosyan A, Copeland NG, Jenkins NA, Kalush F, Mural RJ, Glynne RJ, Kay SA, Adams MD, Fletcher CF.

Proc Natl Acad Sci U S A. 2003 Mar 18;100(6):3380-5. Epub 2003 Feb 28.

9.

Do calcium channel autoantibodies cause cerebellar ataxia with Lambert-Eaton syndrome?

Fletcher CF, Lennon VA.

Ann Neurol. 2003 Jan;53(1):5-7. Review. No abstract available.

PMID:
12509841
10.

Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.

Okazaki Y, Furuno M, Kasukawa T, Adachi J, Bono H, Kondo S, Nikaido I, Osato N, Saito R, Suzuki H, Yamanaka I, Kiyosawa H, Yagi K, Tomaru Y, Hasegawa Y, Nogami A, Schönbach C, Gojobori T, Baldarelli R, Hill DP, Bult C, Hume DA, Quackenbush J, Schriml LM, Kanapin A, Matsuda H, Batalov S, Beisel KW, Blake JA, Bradt D, Brusic V, Chothia C, Corbani LE, Cousins S, Dalla E, Dragani TA, Fletcher CF, Forrest A, Frazer KS, Gaasterland T, Gariboldi M, Gissi C, Godzik A, Gough J, Grimmond S, Gustincich S, Hirokawa N, Jackson IJ, Jarvis ED, Kanai A, Kawaji H, Kawasawa Y, Kedzierski RM, King BL, Konagaya A, Kurochkin IV, Lee Y, Lenhard B, Lyons PA, Maglott DR, Maltais L, Marchionni L, McKenzie L, Miki H, Nagashima T, Numata K, Okido T, Pavan WJ, Pertea G, Pesole G, Petrovsky N, Pillai R, Pontius JU, Qi D, Ramachandran S, Ravasi T, Reed JC, Reed DJ, Reid J, Ring BZ, Ringwald M, Sandelin A, Schneider C, Semple CA, Setou M, Shimada K, Sultana R, Takenaka Y, Taylor MS, Teasdale RD, Tomita M, Verardo R, Wagner L, Wahlestedt C, Wang Y, Watanabe Y, Wells C, Wilming LG, Wynshaw-Boris A, Yanagisawa M, Yang I, Yang L, Yuan Z, Zavolan M, Zhu Y, Zimmer A, Carninci P, Hayatsu N, Hirozane-Kishikawa T, Konno H, Nakamura M, Sakazume N, Sato K, Shiraki T, Waki K, Kawai J, Aizawa K, Arakawa T, Fukuda S, Hara A, Hashizume W, Imotani K, Ishii Y, Itoh M, Kagawa I, Miyazaki A, Sakai K, Sasaki D, Shibata K, Shinagawa A, Yasunishi A, Yoshino M, Waterston R, Lander ES, Rogers J, Birney E, Hayashizaki Y; FANTOM Consortium; RIKEN Genome Exploration Research Group Phase I & II Team.

Nature. 2002 Dec 5;420(6915):563-73.

PMID:
12466851
11.

Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease.

Wilson SM, Bhattacharyya B, Rachel RA, Coppola V, Tessarollo L, Householder DB, Fletcher CF, Miller RJ, Copeland NG, Jenkins NA.

Nat Genet. 2002 Nov;32(3):420-5. Epub 2002 Oct 7.

PMID:
12368914
12.

Mammalian germ-line transgenesis by transposition.

Dupuy AJ, Clark K, Carlson CM, Fritz S, Davidson AE, Markley KM, Finley K, Fletcher CF, Ekker SC, Hackett PB, Horn S, Largaespada DA.

Proc Natl Acad Sci U S A. 2002 Apr 2;99(7):4495-9. Epub 2002 Mar 19.

13.

Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice.

Matesic LE, Yip R, Reuss AE, Swing DA, O'Sullivan TN, Fletcher CF, Copeland NG, Jenkins NA.

Proc Natl Acad Sci U S A. 2001 Aug 28;98(18):10238-43. Epub 2001 Aug 14.

14.

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.

Fletcher CF, Tottene A, Lennon VA, Wilson SM, Dubel SJ, Paylor R, Hosford DA, Tessarollo L, McEnery MW, Pietrobon D, Copeland NG, Jenkins NA.

FASEB J. 2001 May;15(7):1288-90. No abstract available.

PMID:
11344116
15.

Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)).

Mori Y, Wakamori M, Oda S, Fletcher CF, Sekiguchi N, Mori E, Copeland NG, Jenkins NA, Matsushita K, Matsuyama Z, Imoto K.

J Neurosci. 2000 Aug 1;20(15):5654-62.

16.

The status of voltage-dependent calcium channels in alpha 1E knock-out mice.

Wilson SM, Toth PT, Oh SB, Gillard SE, Volsen S, Ren D, Philipson LH, Lee EC, Fletcher CF, Tessarollo L, Copeland NG, Jenkins NA, Miller RJ.

J Neurosci. 2000 Dec 1;20(23):8566-71.

17.

Ataxic mouse mutants and molecular mechanisms of absence epilepsy.

Fletcher CF, Frankel WN.

Hum Mol Genet. 1999;8(10):1907-12. Review.

PMID:
10469844
18.

Mrvi1, a common MRV integration site in BXH2 myeloid leukemias, encodes a protein with homology to a lymphoid-restricted membrane protein Jaw1.

Shaughnessy JD Jr, Largaespada DA, Tian E, Fletcher CF, Cho BC, Vyas P, Jenkins NA, Copeland NG.

Oncogene. 1999 Mar 25;18(12):2069-84.

19.

Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalami.

Caddick SJ, Wang C, Fletcher CF, Jenkins NA, Copeland NG, Hosford DA.

J Neurophysiol. 1999 May;81(5):2066-74.

20.

Exon structure of the nuclear factor I DNA-binding domain from C. elegans to mammals.

Fletcher CF, Jenkins NA, Copeland NG, Chaudhry AZ, Gronostajski RM.

Mamm Genome. 1999 Apr;10(4):390-6.

PMID:
10087299
21.

Genetic analysis of voltage-dependent calcium channels.

Fletcher CF, Copeland NG, Jenkins NA.

J Bioenerg Biomembr. 1998 Aug;30(4):387-98. Review.

PMID:
9758334
22.

Assignment of the mouse Pde7A gene to the proximal region of chromosome 3 and of the human PDE7A gene to chromosome 8q13.

Han P, Fletcher CF, Copeland NG, Jenkins NA, Yaremko LM, Michaeli T.

Genomics. 1998 Mar 1;48(2):275-6. No abstract available.

PMID:
9521885
23.

The cut-homeodomain transcriptional activator HNF-6 is coexpressed with its target gene HNF-3 beta in the developing murine liver and pancreas.

Rausa F, Samadani U, Ye H, Lim L, Fletcher CF, Jenkins NA, Copeland NG, Costa RH.

Dev Biol. 1997 Dec 15;192(2):228-46.

24.

Mouse chromosomal locations of nine genes encoding homologs of human paraneoplastic neurologic disorder antigens.

Fletcher CF, Okano HJ, Gilbert DJ, Yang Y, Yang C, Copeland NG, Jenkins NA, Darnell RB.

Genomics. 1997 Oct 15;45(2):313-9.

PMID:
9344654
25.

Chromosomal mapping of five highly conserved murine homologues of the Drosophila RING finger gene seven-in-absentia.

Holloway AJ, Della NG, Fletcher CF, Largespada DA, Copeland NG, Jenkins NA, Bowtell DD.

Genomics. 1997 Apr 15;41(2):160-8.

PMID:
9143490
26.

Absence epilepsy in tottering mutant mice is associated with calcium channel defects.

Fletcher CF, Lutz CM, O'Sullivan TN, Shaughnessy JD Jr, Hawkes R, Frankel WN, Copeland NG, Jenkins NA.

Cell. 1996 Nov 15;87(4):607-17.

27.

Genesis, a winged helix transcriptional repressor with expression restricted to embryonic stem cells.

Sutton J, Costa R, Klug M, Field L, Xu D, Largaespada DA, Fletcher CF, Jenkins NA, Copeland NG, Klemsz M, Hromas R.

J Biol Chem. 1996 Sep 20;271(38):23126-33.

28.

"Expression patterns of two murine homologs of Drosophila single-minded suggest possible roles in embryonic patterning and in the pathogenesis of Down syndrome.".

Fan CM, Kuwana E, Bulfone A, Fletcher CF, Copeland NG, Jenkins NA, Crews S, Martinez S, Puelles L, Rubenstein LR, Tessier-Lavigne M.

Mol Cell Neurosci. 1996 Jun;7(6):519. No abstract available.

PMID:
8875433
29.

Expression patterns of two murine homologs of Drosophila single-minded suggest possible roles in embryonic patterning and in the pathogenesis of Down syndrome.

Fan CM, Kuwana E, Bulfone A, Fletcher CF, Copeland NG, Jenkins NA, Crews S, Martinez S, Puelles L, Rubenstein JL, Tessier-Lavigne M.

Mol Cell Neurosci. 1996 Jan;7(1):1-16. Erratum in: Mol Cell Neurosci 1996 Jun;7(6):519.

PMID:
8812055
30.

Genomic structure and mapping of precerebellin and a precerebellin-related gene.

Kavety B, Jenkins NA, Fletcher CF, Copeland NG, Morgan JI.

Brain Res Mol Brain Res. 1994 Nov;27(1):152-6.

PMID:
7877445
31.

Isolation of a collagenase cDNA clone and measurement of changing collagenase mRNA levels during induction in rabbit synovial fibroblasts.

Gross RH, Sheldon LA, Fletcher CF, Brinckerhoff CE.

Proc Natl Acad Sci U S A. 1984 Apr;81(7):1981-5.

32.

President's address.

Fletcher CF.

Va Dent J. 1979 Dec;56(6):44-50. No abstract available.

PMID:
298719
33.

Hepatitis B surface antigen (HBsAg) and its antibody (HBsAb) among dentists and auxiliary personnel in Virginia.

Escobar MR, Syrop HM, Fisher LM, Swenson PD, Blanke RV, Fletcher CF.

Va Dent J. 1978 Jun;55(3):22-7. No abstract available.

PMID:
287295
34.

Combating the illegal practice of dentistry.

Fletcher CF.

J Prosthet Dent. 1976 Jan;35(1):92-6.

PMID:
1062592
35.

The cochlear geometry as a frequency analyser. Further experimental observations on models.

Naftalin L, Fletcher CF.

J Laryngol Otol. 1974 Jul;88(7):675-8. No abstract available.

PMID:
4418399
36.

The Virginia program for implementing the work authorization law.

Martone AL, Fletcher CF, Wendt DC.

J Am Dent Assoc. 1966 May;72(5):1122-9. No abstract available.

PMID:
5218064

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