Smith A - Search Results

1

Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray genotyping.

Pask R, Rance HE, Barratt BJ, Nutland S, Smyth DJ, Sebastian M, Twells RC, Smith A, Lam AC, Smink LJ, Walker NM, Todd JA. Pask R, et al. Among authors: smith a. BMC Biotechnol. 2004 Jul 27;4:15. doi: 10.1186/1472-6750-4-15. BMC Biotechnol. 2004. PMID: 15279678 Free PMC article.

2

Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.

Nejentsev S, Smink LJ, Smyth D, Bailey R, Lowe CE, Payne F, Masters J, Godfrey L, Lam A, Burren O, Stevens H, Nutland S, Walker NM, Smith A, Twells R, Barratt BJ, Wright C, French L, Chen Y, Deloukas P, Rogers J, Dunham I, Todd JA. Nejentsev S, et al. Among authors: smith a. BMC Genet. 2007 May 17;8:24. doi: 10.1186/1471-2156-8-24. BMC Genet. 2007. PMID: 17509149 Free PMC article.

3

Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation.

Mein CA, Barratt BJ, Dunn MG, Siegmund T, Smith AN, Esposito L, Nutland S, Stevens HE, Wilson AJ, Phillips MS, Jarvis N, Law S, de Arruda M, Todd JA. Mein CA, et al. Among authors: smith an. Genome Res. 2000 Mar;10(3):330-43. doi: 10.1101/gr.10.3.330. Genome Res. 2000. PMID: 10720574 Free PMC article.

4

Haplotype tagging for the identification of common disease genes.

Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA. Johnson GC, et al. Among authors: smith an. Nat Genet. 2001 Oct;29(2):233-7. doi: 10.1038/ng1001-233. Nat Genet. 2001. PMID: 11586306

5

Candidate gene association study of solute carrier family 11a members 1 (SLC11A1) and 2 (SLC11A2) genes in Alzheimer's disease.

Jamieson SE, White JK, Howson JM, Pask R, Smith AN, Brayne C, Evans JG, Xuereb J, Cairns NJ, Rubinsztein DC, Blackwell JM. Jamieson SE, et al. Neurosci Lett. 2005 Feb 10;374(2):124-8. doi: 10.1016/j.neulet.2004.10.038. Neurosci Lett. 2005. PMID: 15644277

6

A search for type 1 diabetes susceptibility genes in families from the United Kingdom.

Mein CA, Esposito L, Dunn MG, Johnson GC, Timms AE, Goy JV, Smith AN, Sebag-Montefiore L, Merriman ME, Wilson AJ, Pritchard LE, Cucca F, Barnett AH, Bain SC, Todd JA. Mein CA, et al. Among authors: smith an. Nat Genet. 1998 Jul;19(3):297-300. doi: 10.1038/991. Nat Genet. 1998. PMID: 9662409

7

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss.

Stover EH, Borthwick KJ, Bavalia C, Eady N, Fritz DM, Rungroj N, Giersch AB, Morton CC, Axon PR, Akil I, Al-Sabban EA, Baguley DM, Bianca S, Bakkaloglu A, Bircan Z, Chauveau D, Clermont MJ, Guala A, Hulton SA, Kroes H, Li Volti G, Mir S, Mocan H, Nayir A, Ozen S, Rodriguez Soriano J, Sanjad SA, Tasic V, Taylor CM, Topaloglu R, Smith AN, Karet FE. Stover EH, et al. Among authors: smith an. J Med Genet. 2002 Nov;39(11):796-803. doi: 10.1136/jmg.39.11.796. J Med Genet. 2002. PMID: 12414817 Free PMC article.

8

Molecular cloning and characterization of Atp6n1b: a novel fourth murine vacuolar H+-ATPase a-subunit gene.

Smith AN, Finberg KE, Wagner CA, Lifton RP, Devonald MA, Su Y, Karet FE. Smith AN, et al. J Biol Chem. 2001 Nov 9;276(45):42382-8. doi: 10.1074/jbc.M107267200. Epub 2001 Aug 8. J Biol Chem. 2001. PMID: 11495928 Free article.

9

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing.

Smith AN, Skaug J, Choate KA, Nayir A, Bakkaloglu A, Ozen S, Hulton SA, Sanjad SA, Al-Sabban EA, Lifton RP, Scherer SW, Karet FE. Smith AN, et al. Nat Genet. 2000 Sep;26(1):71-5. doi: 10.1038/79208. Nat Genet. 2000. PMID: 10973252

10

Self-monitoring of blood pressure following a stroke or transient ischaemic attack (TASMIN5S): a randomised controlled trial.

McManus RJ, Smith A, Temple E, Yu LM, Allen J, Doogue R, Ford GA, Glynn L, Guthrie B, Hall P, Hinton L, Hobbs FDR, Mant J, McKinstry B, Mead G, Morton K, Rai T, Rice C, Roman C, Stoddart A, Tarassenko L, Velardo C, Williams M, Yardley L; TASMIN5S investigators. McManus RJ, et al. Among authors: smith a. BMC Cardiovasc Disord. 2024 Dec 27;24(1):746. doi: 10.1186/s12872-024-04320-0. BMC Cardiovasc Disord. 2024. PMID: 39731065 Clinical Trial.

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