| Year |
Citation |
Score |
| 2005 |
Carter TA, Greenhall JA, Yoshida S, Fuchs S, Helton R, Swaroop A, Lockhart DJ, Barlow C. Mechanisms of aging in senescence-accelerated mice. Genome Biology. 6: R48. PMID 15960800 DOI: 10.1186/Gb-2005-6-6-R48 |
0.304 |
|
| 2004 |
Yoshida S, Mears AJ, Friedman JS, Carter T, He S, Oh E, Jing Y, Farjo R, Fleury G, Barlow C, Hero AO, Swaroop A. Expression profiling of the developing and mature Nrl-/- mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl. Human Molecular Genetics. 13: 1487-503. PMID 15163632 DOI: 10.1093/Hmg/Ddh160 |
0.408 |
|
| 2004 |
Yu J, Mears AJ, Yoshida S, Farjo R, Carter TA, Ghosh D, Hero A, Barlow C, Swaroop A. From disease genes to cellular pathways: a progress report. Novartis Foundation Symposium. 255: 147-60; discussion 1. PMID 14750602 DOI: 10.1002/0470092645.Ch11 |
0.455 |
|
| 2003 |
Scheel JR, Garrett LJ, Allen DM, Carter TA, Randolph-Moore L, Gambello MJ, Gage FH, Wynshaw-Boris A, Barlow C. An inbred 129SvEv GFPCre transgenic mouse that deletes loxP-flanked genes in all tissues. Nucleic Acids Research. 31: e57. PMID 12736323 DOI: 10.1093/Nar/Gng057 |
0.425 |
|
| 2001 |
Carter TA, Del Rio JA, Greenhall JA, Latronica ML, Lockhart DJ, Barlow C. Chipping away at complex behavior: transcriptome/phenotype correlations in the mouse brain. Physiology & Behavior. 73: 849-57. PMID 11566218 DOI: 10.1016/S0031-9384(01)00522-4 |
0.446 |
|
| 2001 |
Allen DM, van Praag H, Ray J, Weaver Z, Winrow CJ, Carter TA, Braquet R, Harrington E, Ried T, Brown KD, Gage FH, Barlow C. Ataxia telangiectasia mutated is essential during adult neurogenesis. Genes & Development. 15: 554-66. PMID 11238376 DOI: 10.1101/Gad.869001 |
0.351 |
|
| 2000 |
Kaneshige M, Kaneshige K, Zhu X, Dace A, Garrett L, Carter TA, Kazlauskaite R, Pankratz DG, Wynshaw-Boris A, Refetoff S, Weintraub B, Willingham MC, Barlow C, Cheng S. Mice with a targeted mutation in the thyroid hormone beta receptor gene exhibit impaired growth and resistance to thyroid hormone. Proceedings of the National Academy of Sciences of the United States of America. 97: 13209-14. PMID 11069286 DOI: 10.1073/Pnas.230285997 |
0.375 |
|
| 2000 |
Sandberg R, Yasuda R, Pankratz DG, Carter TA, Del Rio JA, Wodicka L, Mayford M, Lockhart DJ, Barlow C. Regional and strain-specific gene expression mapping in the adult mouse brain. Proceedings of the National Academy of Sciences of the United States of America. 97: 11038-43. PMID 11005875 DOI: 10.1073/Pnas.97.20.11038 |
0.39 |
|
| 1997 |
Wang CH, Carter TA, Das K, Xu J, Ross BM, Penchaszadeh GK, Gilliam TC. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues. Annals of Neurology. 42: 41-9. PMID 9225684 DOI: 10.1002/Ana.410420109 |
0.589 |
|
| 1997 |
Carter TA, Bönnemann CG, Wang CH, Obici S, Parano E, De Fatima Bonaldo M, Ross BM, Penchaszadeh GK, Mackenzie A, Soares MB, Kunkel LM, Gilliam TC. A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions. Human Molecular Genetics. 6: 229-36. PMID 9063743 DOI: 10.1093/Hmg/6.2.229 |
0.601 |
|
| 1996 |
Wang CH, Xu J, Carter TA, Ross BM, Dominski MK, Bellcross CA, Penchaszadeh GK, Munsat TL, Gilliam TC. Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy. Human Molecular Genetics. 5: 359-65. PMID 8852661 DOI: 10.1093/Hmg/5.3.359 |
0.587 |
|
| 1994 |
Wang CH, Kleyn PW, Xu J, Vitale E, Carter TA, Ross BM, Das K, Soares MB, Brzustowicz LM, Kunkel LM, Conrad Gilliam T. Isolation of coding sequences and evaluation of candidate genes for spinal muscular atrophy Pediatric Neurology. 11: 101. DOI: 10.1016/0887-8994(94)90206-2 |
0.39 |
|
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