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Results: 1 to 20 of 27

1.

Differential expression of miR-17~92 identifies BCL2 as a therapeutic target in BCR-ABL-positive B-lineage acute lymphoblastic leukemia.

Scherr M, Elder A, Battmer K, Barzan D, Bomken S, Ricke-Hoch M, Schröder A, Venturini L, Blair HJ, Vormoor J, Ottmann O, Ganser A, Pich A, Hilfiker-Kleiner D, Heidenreich O, Eder M.

Leukemia. 2014 Mar;28(3):554-65. doi: 10.1038/leu.2013.361. Epub 2013 Nov 27.

PMID:
24280866
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Evc regulates a symmetrical response to Shh signaling in molar development.

Nakatomi M, Hovorakova M, Gritli-Linde A, Blair HJ, MacArthur K, Peterka M, Lesot H, Peterkova R, Ruiz-Perez VL, Goodship JA, Peters H.

J Dent Res. 2013 Mar;92(3):222-8. doi: 10.1177/0022034512471826. Epub 2013 Jan 11.

PMID:
23315474
[PubMed - indexed for MEDLINE]
3.

Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleus.

Blair HJ, Tompson S, Liu YN, Campbell J, MacArthur K, Ponting CP, Ruiz-Perez VL, Goodship JA.

BMC Biol. 2011 Feb 28;9:14. doi: 10.1186/1741-7007-9-14.

PMID:
21356043
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Evc is a positive mediator of Ihh-regulated bone growth that localises at the base of chondrocyte cilia.

Ruiz-Perez VL, Blair HJ, Rodriguez-Andres ME, Blanco MJ, Wilson A, Liu YN, Miles C, Peters H, Goodship JA.

Development. 2007 Aug;134(16):2903-12.

PMID:
17660199
[PubMed - indexed for MEDLINE]
Free Article
5.

Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis-van Creveld syndrome patients.

Tompson SW, Ruiz-Perez VL, Blair HJ, Barton S, Navarro V, Robson JL, Wright MJ, Goodship JA.

Hum Genet. 2007 Jan;120(5):663-70. Epub 2006 Sep 21.

PMID:
17024374
[PubMed - indexed for MEDLINE]
6.

Suicide and self-harm following prescription of SSRIs and other antidepressants: confounding by indication.

Didham RC, McConnell DW, Blair HJ, Reith DM.

Br J Clin Pharmacol. 2005 Nov;60(5):519-25.

PMID:
16236042
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy.

Garcia CC, Blair HJ, Seager M, Coulthard A, Tennant S, Buddles M, Curtis A, Goodship JA.

J Med Genet. 2004 Mar;41(3):183-6.

PMID:
14985377
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Mutations in two nonhomologous genes in a head-to-head configuration cause Ellis-van Creveld syndrome.

Ruiz-Perez VL, Tompson SW, Blair HJ, Espinoza-Valdez C, Lapunzina P, Silva EO, Hamel B, Gibbs JL, Young ID, Wright MJ, Goodship JA.

Am J Hum Genet. 2003 Mar;72(3):728-32. Epub 2003 Feb 4.

PMID:
12571802
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome.

Blair HJ, Reed V, Gormally E, Wilson JB, Novak J, McInnes RR, Phillips SJ, Taylor BA, Boyd Y.

Mamm Genome. 2000 Aug;11(8):710-2. No abstract available.

PMID:
10920247
[PubMed - indexed for MEDLINE]
10.

A phenotype map of the mouse X chromosome: models for human X-linked disease.

Boyd Y, Blair HJ, Cunliffe P, Masson WK, Reed V.

Genome Res. 2000 Mar;10(3):277-92. Review.

PMID:
10720569
[PubMed - indexed for MEDLINE]
Free Article
11.

Encyclopedia of the mouse genome VII. Mouse chromosome X.

Boyd Y, Blair HJ, Cunliffe P, Denny P, Gormally E, Herman GE.

Mamm Genome. 1998;8 Spec No:S361-77. No abstract available.

PMID:
9662637
[PubMed - indexed for MEDLINE]
12.

Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis.

Blair HJ, Gormally E, Uwechue IC, Boyd Y.

Hum Mol Genet. 1998 Mar;7(3):549-55.

PMID:
9467016
[PubMed - indexed for MEDLINE]
Free Article
13.

An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome.

Blair HJ, Uwechue IC, Barsh GS, Rowe PS, Boyd Y.

Genomics. 1998 Feb 15;48(1):128-31.

PMID:
9503026
[PubMed - indexed for MEDLINE]
14.

The structure of DXF34, a human X-linked sequence family with homology to a transcribed mouse Y-linked repeat.

Laval SH, Reed V, Blair HJ, Boyd Y.

Mamm Genome. 1997 Sep;8(9):689-91. No abstract available.

PMID:
9271673
[PubMed - indexed for MEDLINE]
15.

Mouse X chromosome.

Boyd Y, Herman GE, Avner P, Disteche CM, Adler D, Reed V, Blair HJ.

Mamm Genome. 1997;7 Spec No:S313-26. No abstract available.

PMID:
9233403
[PubMed - indexed for MEDLINE]
16.

The mouse X-linked developmental mutant, tattered, lies between DXMit55 and Xkh and is associated with hyperkeratinization.

Uwechue IC, Cooper BF, Goble C, Hacker T, Blair HJ, Burke DT, Herman G, Boyd Y.

Genomics. 1996 Oct 15;37(2):238-41.

PMID:
8921395
[PubMed - indexed for MEDLINE]
17.

Smcx lies distal to DXHX674 and DXHX679 on the mouse X chromosome.

Laval SH, Blair HJ, Mitchell MJ, Boyd Y.

Mamm Genome. 1996 Jul;7(7):552. No abstract available.

PMID:
8672147
[PubMed - indexed for MEDLINE]
18.

Encyclopedia of the mouse genome V. Mouse X chromosome.

Herman GE, Blair HJ, Boyd SD, de Gouyon B, Haynes A, Quaderi N.

Mamm Genome. 1996;6 Spec No:S317-30. No abstract available.

PMID:
8800776
[PubMed - indexed for MEDLINE]
19.

High-resolution comparative mapping of the proximal region of the mouse X chromosome.

Blair HJ, Ho M, Monaco AP, Fisher S, Craig IW, Boyd Y.

Genomics. 1995 Jul 20;28(2):305-10.

PMID:
8530041
[PubMed - indexed for MEDLINE]
20.

Evaluation of human microdissection clones from the FRAXA region as tools for comparative mapping in the mouse: isolation of a conserved genomic clone close to FMR1.

Blair HJ, Hirst MC, MacKinnon R, Davies KE, Boyd Y.

Mamm Genome. 1994 Sep;5(9):584-7. No abstract available.

PMID:
8000145
[PubMed - indexed for MEDLINE]

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