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Items: 1 to 50 of 65

1.

Recombination hotspots and block structure of linkage disequilibrium in the human genome exemplified by detailed analysis of PGM1 on 1p31.

Rana NA, Ebenezer ND, Webster AR, Linares AR, Whitehouse DB, Povey S, Hardcastle AJ.

Hum Mol Genet. 2004 Dec 15;13(24):3089-102. Epub 2004 Oct 27.

PMID:
15509594
2.

Alpha1-antitrypsin as a risk for infant and adult respiratory outcomes in a national birth cohort.

Wadsworth ME, Vinall LE, Jones AL, Hardy RJ, Whitehouse DB, Butterworth SL, Hilder WS, Lovegrove JU, Swallow DM.

Am J Respir Cell Mol Biol. 2004 Nov;31(5):559-64. Epub 2004 Jul 22.

PMID:
15271689
3.

New monoclonal antibodies to non-glycosylated domains of the secreted mucins MUC5B and MUC7.

Rousseau K, Wickstrom C, Whitehouse DB, Carlstedt I, Swallow DM.

Hybrid Hybridomics. 2003 Oct;22(5):293-9.

PMID:
14678646
4.

Progression of atherosclerosis is associated with variation in the alpha1-antitrypsin gene.

Talmud PJ, Martin S, Steiner G, Flavell DM, Whitehouse DB, Nagl S, Jackson R, Taskinen MR, Frick MH, Nieminen MS, Kesäniemi YA, Pasternack A, Humphries SE, Syvänne M; Diabetes Atherosclerosis Intervention Study Investigators.

Arterioscler Thromb Vasc Biol. 2003 Apr 1;23(4):644-9. Epub 2003 Mar 6.

PMID:
12692006
5.

Identification of alpha(1)-antitrypsin variants in plasma with the use of proteomic technology.

Mills K, Mills PB, Clayton PT, Johnson AW, Whitehouse DB, Winchester BG.

Clin Chem. 2001 Nov;47(11):2012-22.

6.

Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1).

Yip SP, Putt W, Hopkinson DA, Whitehouse DB.

Ann Hum Genet. 1999 Mar;63(Pt 2):129-40.

PMID:
10738524
7.

Anti-neutrophil cytoplasmic antibodies (ANCA) against bactericidal/permeability-increasing protein (BPI) and cystic fibrosis lung disease.

Mahadeva R, Dunn AC, Westerbeek RC, Sharples L, Whitehouse DB, Carroll NR, Ross-Russell RI, Webb AK, Bilton D, Lomas DA, Lockwood CM.

Clin Exp Immunol. 1999 Sep;117(3):561-7.

8.

Mapping recombination hotspots in human phosphoglucomutase (PGM1).

Yip SP, Lovegrove JU, Rana NA, Hopkinson DA, Whitehouse DB.

Hum Mol Genet. 1999 Sep;8(9):1699-706.

PMID:
10441333
9.

Improvement of SSCP analysis by use of denaturants.

Yip SP, Hopkinson DA, Whitehouse DB.

Biotechniques. 1999 Jul;27(1):20-2, 24. No abstract available.

10.

Alpha1-antitrypsin deficiency alleles and the Taq-I G-->A allele in cystic fibrosis lung disease.

Mahadeva R, Westerbeek RC, Perry DJ, Lovegrove JU, Whitehouse DB, Carroll NR, Ross-Russell RI, Webb AK, Bilton D, Lomas DA.

Eur Respir J. 1998 Apr;11(4):873-9.

11.

A phylogenetic approach to the identification of phosphoglucomutase genes.

Whitehouse DB, Tomkins J, Lovegrove JU, Hopkinson DA, McMillan WO.

Mol Biol Evol. 1998 Apr;15(4):456-62.

PMID:
9549096
12.

A new alpha 1-antitrypsin mutation, Thr-Met 85, (PI Zbristol) associated with novel electrophoretic properties.

Lovegrove JU, Jeremiah S, Gillett GT, Temple IK, Povey S, Whitehouse DB.

Ann Hum Genet. 1997 Sep;61(Pt 5):385-91.

13.

Molecular and cytological investigations of phosphoglucomutase (PGM1) in the K562 cell line.

Tomkins J, Fox M, Lovegrove JU, Parrington J, Hopkinson DA, Whitehouse DB.

Ann Hum Genet. 1997 Mar;61(Pt 2):99-108.

14.
15.

DNA polymorphisms in the lactase gene. Linkage disequilibrium across the 70-kb region.

Harvey CB, Pratt WS, Islam I, Whitehouse DB, Swallow DM.

Eur J Hum Genet. 1995;3(1):27-41.

PMID:
7767654
16.

Lack of association between maternal phosphoglucomutase-1 phenotype and fetal macrosomia in diabetic pregnancy.

Johnstone FD, West JD, Steel J, Whitehouse DB, Drago GA, Greer IA, Prescott RJ.

Br J Obstet Gynaecol. 1994 Mar;101(3):239-45.

PMID:
8193100
17.

'SZ like' alpha 1-antitrypsin phenotypes in PI ZZ children with liver disease.

Whitehouse DB, Lovegrove JU, Mieli-Vergani G, Mowat AP, Hopkinson DA.

Ann Hum Genet. 1994 Jan;58(1):11-7.

PMID:
8031012
18.
19.

Phosphoglucomutase 1: a gene with two promoters and a duplicated first exon.

Putt W, Ives JH, Hollyoake M, Hopkinson DA, Whitehouse DB, Edwards YH.

Biochem J. 1993 Dec 1;296 ( Pt 2):417-22.

20.

Fetal growth, gestation length and phosphoglucomutase-1 phenotype.

Johnstone FD, West JD, Prescott RJ, Steel JM, Flockhart JA, Greer IA, Drago GA, Whitehouse DB.

Dis Markers. 1993 Dec;11(5-6):251-62.

PMID:
8082314
21.

The classical human phosphoglucomutase (PGM1) isozyme polymorphism is generated by intragenic recombination.

March RE, Putt W, Hollyoake M, Ives JH, Lovegrove JU, Hopkinson DA, Edwards YH, Whitehouse DB.

Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10730-3.

22.

Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 cases.

Abbott CM, Lovegrove JU, Whitehouse DB, Hopkinson DA, Povey S.

Prenat Diagn. 1993 Jun;13(6):544. No abstract available.

PMID:
8372083
23.

Genetic polymorphism in the 3' untranslated region of human phosphoglucomutase-1.

March RE, Hollyoake M, Putt W, Hopkinson DA, Edwards YH, Whitehouse DB.

Ann Hum Genet. 1993 Jan;57(1):1-8.

PMID:
8333728
24.

A monoclonal antibody to alcohol dehydrogenase cross-reacts with human complement component C3.

Leone NA, Whitehouse DB, Swallow DM, Adinolfi A.

Exp Clin Immunogenet. 1993;10(1):50-5.

PMID:
7691112
25.

Two TaqI polymorphisms at the human PGM1 locus.

Hollyoake M, Putt W, Edwards YH, Whitehouse DB.

Hum Mol Genet. 1992 Aug;1(5):354. No abstract available.

PMID:
1363877
26.

Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 cases.

Abbott CM, Lovegrove JU, Whitehouse DB, Hopkinson DA, Povey S.

Prenat Diagn. 1992 Apr;12(4):235-40. Erratum in: Prenat Diagn 1993 Jun;13(6):544.

PMID:
1614981
27.

Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1.

Whitehouse DB, Putt W, Lovegrove JU, Morrison K, Hollyoake M, Fox MF, Hopkinson DA, Edwards YH.

Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):411-5.

28.

Antigenic analysis of the major human phosphoglucomutase isozymes: PGM1, PGM2, PGM3 and PGM4.

Drago GA, Hopkinson DA, Westwood SA, Whitehouse DB.

Ann Hum Genet. 1991 Oct;55(4):263-71.

PMID:
1840235
29.

HLA phenotypes and gene polymorphisms in juvenile liver disease associated with alpha 1-antitrypsin deficiency.

Doherty DG, Donaldson PT, Whitehouse DB, Mieli-Vergani G, Duthie A, Hopkinson DA, Mowat AP.

Hepatology. 1990 Aug;12(2):218-23.

PMID:
1975247
30.

Genetic studies on a new deficiency gene (PI*Ztun) at the PI locus.

Whitehouse DB, Abbott CM, Lovegrove JU, McIntosh I, McMahon CJ, Mieli-Vergani G, Mowat AP, Hopkinson DA.

J Med Genet. 1989 Dec;26(12):744-9.

31.
32.

Isozyme and DNA analysis of human S-adenosyl-L-homocysteine hydrolase (AHCY).

Arredondo-Vega FX, Charlton JA, Edwards YH, Hopkinson DA, Whitehouse DB.

Ann Hum Genet. 1989 May;53(2):157-67.

PMID:
2574561
33.

Immunological detection of human phosphoglucomutase (PGM 1) subtypes.

Whitehouse DB, Drago GA, Hopkinson DA, Westwood SA, Werrett DJ.

Forensic Sci Int. 1989 Apr-May;41(1-2):25-34.

PMID:
2527794
34.

Rhodanese isozymes in three subjects with Leber's optic neuropathy.

Whitehouse DB, Poole CJ, Kind PR, Hopkinson DA.

J Med Genet. 1989 Feb;26(2):113-5.

35.

Variation in alpha-1-antitrypsin phenotypes associated with penicillamine therapy.

Whitehouse DB, Lovegrove JU, Hopkinson DA.

Clin Chim Acta. 1989 Jan 13;179(1):109-15.

PMID:
2784082
36.

Inheritance and linkage data for an unusual combination of genes (at the LKE, PI and C6 loci) in a single large sibship.

Whitehouse DB, Attwood J, Green C, Bruce M, McQuade M, Tippett P.

Ann Hum Genet. 1988 Jul;52(3):197-201.

PMID:
3250330
37.

Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction.

Abbott CM, McMahon CJ, Whitehouse DB, Povey S.

Lancet. 1988 Apr 2;1(8588):763-4. No abstract available.

PMID:
2895285
38.

Rhodanese isozymes in human tissues.

Whitehouse DB, Pilz AJ, Porta G, Hopkinson DA.

Ann Hum Genet. 1988 Jan;52(1):1-10.

PMID:
3178139
39.

Genetic polymorphisms of animal complement components.

Whitehouse DB.

Exp Clin Immunogenet. 1988;5(2-3):143-64. Review.

PMID:
3078568
40.

Alpha 1-antitrypsin-related gene (ATR) for prenatal diagnosis.

Abbott CM, McMahon CJ, Kelsey GD, Parkar M, Whitehouse DB, Corney G, Povey S, Hopkinson DA, Mieli-Vergani G, Mowat A.

Lancet. 1987 Jun 20;1(8547):1425-6. No abstract available.

PMID:
2884507
41.

Prenatal diagnosis of alpha-1-antitrypsin deficiency by fetal blood sampling.

Corney G, Whitehouse DB, Hopkinson DA, Rodeck CH, Nicolaides K, Norman M, Mowat AP.

Prenat Diagn. 1987 Feb;7(2):101-8.

PMID:
3494989
42.

Sensitive techniques for the detection of genetic variation in human isozymes.

Whitehouse DB, Hopkinson DA.

Isozymes Curr Top Biol Med Res. 1987;16:101-24.

PMID:
3610587
43.

Ahaptoglobinaemia in Melanesia: DNA and malarial antibody studies.

Hill AV, Whitehouse DB, Bowden DK, Hopkinson DA, Draper CC, Peto TE, Clegg JB, Weatherall DJ.

Trans R Soc Trop Med Hyg. 1987;81(4):573-7.

PMID:
3328345
44.

A population genetic survey of the haptoglobin polymorphism in Melanesians by DNA analysis.

Hill AV, Bowden DK, Flint J, Whitehouse DB, Hopkinson DA, Oppenheimer SJ, Serjeantson SW, Clegg JB.

Am J Hum Genet. 1986 Mar;38(3):382-9.

45.

Adenosine deaminase activity in a series of 19 patients with the Diamond-Blackfan syndrome.

Whitehouse DB, Hopkinson DA, Pilz AJ, Arredondo FX.

Adv Exp Med Biol. 1986;195 Pt A:85-92. No abstract available.

PMID:
3728189
46.

Analysis of genetic variation in two human thyroxine-binding plasma proteins by immunodetection after isoelectric focusing.

Whitehouse DB, Hopkinson DA, Hill AV, Bowden DK.

Ann Hum Genet. 1985 Oct;49(4):259-65.

PMID:
3935040
47.
48.

Adenosine deaminase activity in Diamond-Blackfan syndrome.

Whitehouse DB, Hopkinson DA, Evans DI.

Lancet. 1984 Dec 15;2(8416):1398-9. No abstract available.

PMID:
6150395
49.

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