Halford S - Search Results

1

Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2.

Inglis-Broadgate SL, Ocaka L, Banerjee R, Gaasenbeek M, Chapple JP, Cheetham ME, Clark BJ, Hunt DM, Halford S. Inglis-Broadgate SL, et al. Among authors: halford s. Gene. 2005 Aug 15;356:19-31. doi: 10.1016/j.gene.2005.04.037. Gene. 2005. PMID: 16023307

2

Isolation and chromosomal localization of two human CDP-diacylglycerol synthase (CDS) genes.

Halford S, Dulai KS, Daw SC, Fitzgibbon J, Hunt DM. Halford S, et al. Genomics. 1998 Nov 15;54(1):140-4. doi: 10.1006/geno.1998.5547. Genomics. 1998. PMID: 9806839

3

Assignment of claudin-1 (CLDN1) to human chromosome 3q28-->q29 with somatic cell hybrids.

Halford S, Spencer P, Greenwood J, Winton H, Hunt DM, Adamson P. Halford S, et al. Cytogenet Cell Genet. 2000;88(3-4):217. doi: 10.1159/000015553. Cytogenet Cell Genet. 2000. PMID: 10828592 No abstract available.

4

Characterization of a novel human opsin gene with wide tissue expression and identification of embedded and flanking genes on chromosome 1q43.

Halford S, Freedman MS, Bellingham J, Inglis SL, Poopalasundaram S, Soni BG, Foster RG, Hunt DM. Halford S, et al. Genomics. 2001 Mar 1;72(2):203-8. doi: 10.1006/geno.2001.6469. Genomics. 2001. PMID: 11401433

5

Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy.

El-Ashry MF, Abd El-Aziz MM, Wilkins S, Cheetham ME, Wilkie SE, Hardcastle AJ, Halford S, Bayoumi AY, Ficker LA, Tuft S, Bhattacharya SS, Ebenezer ND. El-Ashry MF, et al. Among authors: halford s. Invest Ophthalmol Vis Sci. 2002 Feb;43(2):377-82. Invest Ophthalmol Vis Sci. 2002. PMID: 11818380

6

Assignment of panopsin (OPN3) to human chromosome band 1q43 by in situ hybridization and somatic cell hybrids.

Halford S, Bellingham J, Ocaka L, Fox M, Johnson S, Foster RG, Hunt DM. Halford S, et al. Cytogenet Cell Genet. 2001;95(3-4):234-5. doi: 10.1159/000059351. Cytogenet Cell Genet. 2001. PMID: 12063405 No abstract available.

7

Genomic organization of human CDS2 and evaluation as a candidate gene for corneal hereditary endothelial dystrophy 2 on chromosome 20p13.

Halford S, Inglis S, Gwilliam R, Spencer P, Mohamed M, Ebenezer ND, Hunt DM. Halford S, et al. Exp Eye Res. 2002 Nov;75(5):619-23. doi: 10.1006/exer.2002.2052. Exp Eye Res. 2002. PMID: 12457874 No abstract available.

8

Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).

Johnson S, Halford S, Morris AG, Patel RJ, Wilkie SE, Hardcastle AJ, Moore AT, Zhang K, Hunt DM. Johnson S, et al. Among authors: halford s. Genomics. 2003 Mar;81(3):304-14. doi: 10.1016/s0888-7543(03)00010-7. Genomics. 2003. PMID: 12659814

9

Chromosomal localization, genomic organization and evolution of the genes encoding human phosphatidylinositol transfer protein membrane-associated (PITPNM) 1, 2 and 3.

Ocaka L, Spalluto C, Wilson DI, Hunt DM, Halford S. Ocaka L, et al. Among authors: halford s. Cytogenet Genome Res. 2005;108(4):293-302. doi: 10.1159/000081519. Cytogenet Genome Res. 2005. PMID: 15627748

10

Differential expression of two distinct functional isoforms of melanopsin (Opn4) in the mammalian retina.

Pires SS, Hughes S, Turton M, Melyan Z, Peirson SN, Zheng L, Kosmaoglou M, Bellingham J, Cheetham ME, Lucas RJ, Foster RG, Hankins MW, Halford S. Pires SS, et al. Among authors: halford s. J Neurosci. 2009 Sep 30;29(39):12332-42. doi: 10.1523/JNEUROSCI.2036-09.2009. J Neurosci. 2009. PMID: 19793992 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

281 results

Search Page

Filters