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Items: 1 to 50 of 110

1.
2.

Identification and functional characterization of polymorphisms in human cyclooxygenase-1 (PTGS1).

Lee CR, Bottone FG Jr, Krahn JM, Li L, Mohrenweiser HW, Cook ME, Petrovich RM, Bell DA, Eling TE, Zeldin DC.

Pharmacogenet Genomics. 2007 Feb;17(2):145-60.

3.

Exploration of methods to identify polymorphisms associated with variation in DNA repair capacity phenotypes.

Jones IM, Thomas CB, Xi T, Mohrenweiser HW, Nelson DO.

Mutat Res. 2007 Mar 1;616(1-2):213-20. Epub 2006 Dec 4.

PMID:
17145065
4.

Four human FANCG polymorphic variants show normal biological function in hamster CHO cells.

Hinz JM, Nham PB, Yamada NA, Tebbs RS, Salazar EP, Hinz AK, Mohrenweiser HW, Jones IM, Thompson LH.

Mutat Res. 2006 Dec 1;602(1-2):34-42. Epub 2006 Sep 28.

PMID:
17010390
5.

The genetic basis for variation in radiation sensitivity in the general population.

Jones IM, Thomas CB, Xi T, Nelson DO, Mohrenweiser HW.

Radiat Res. 2005 Jun;163(6):700-1. No abstract available.

PMID:
16044501
6.

Functional consequences of single nucleotide polymorphisms in the human organic anion transporter hOAT1 (SLC22A6).

Bleasby K, Hall LA, Perry JL, Mohrenweiser HW, Pritchard JB.

J Pharmacol Exp Ther. 2005 Aug;314(2):923-31. Epub 2005 May 24.

PMID:
15914676
7.
9.

A prospective study of XRCC1 haplotypes and their interaction with plasma carotenoids on breast cancer risk.

Han J, Hankinson SE, De Vivo I, Spiegelman D, Tamimi RM, Mohrenweiser HW, Colditz GA, Hunter DJ.

Cancer Res. 2003 Dec 1;63(23):8536-41.

10.

DNA-repair genetic polymorphisms and breast cancer risk.

Smith TR, Levine EA, Perrier ND, Miller MS, Freimanis RI, Lohman K, Case LD, Xu J, Mohrenweiser HW, Hu JJ.

Cancer Epidemiol Biomarkers Prev. 2003 Nov;12(11 Pt 1):1200-4.

11.

Genetic findings and functional studies of human CYP3A5 single nucleotide polymorphisms in different ethnic groups.

Lee SJ, Usmani KA, Chanas B, Ghanayem B, Xi T, Hodgson E, Mohrenweiser HW, Goldstein JA.

Pharmacogenetics. 2003 Aug;13(8):461-72.

PMID:
12893984
12.

Polymorphisms in human soluble epoxide hydrolase.

Przybyla-Zawislak BD, Srivastava PK, Vazquez-Matias J, Mohrenweiser HW, Maxwell JE, Hammock BD, Bradbury JA, Enayetallah AE, Zeldin DC, Grant DF.

Mol Pharmacol. 2003 Aug;64(2):482-90.

PMID:
12869654
13.
14.

Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer.

Smith TR, Miller MS, Lohman K, Lange EM, Case LD, Mohrenweiser HW, Hu JJ.

Cancer Lett. 2003 Feb 20;190(2):183-90.

PMID:
12565173
15.

Symposium overview: genetic polymorphisms in DNA repair and cancer risk.

Hu JJ, Mohrenweiser HW, Bell DA, Leadon SA, Miller MS.

Toxicol Appl Pharmacol. 2002 Nov 15;185(1):64-73.

PMID:
12460738
16.

Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans.

Mohrenweiser HW, Xi T, Vázquez-Matías J, Jones IM.

Cancer Epidemiol Biomarkers Prev. 2002 Oct;11(10 Pt 1):1054-64.

17.

Identification of variants of CYP3A4 and characterization of their abilities to metabolize testosterone and chlorpyrifos.

Dai D, Tang J, Rose R, Hodgson E, Bienstock RJ, Mohrenweiser HW, Goldstein JA.

J Pharmacol Exp Ther. 2001 Dec;299(3):825-31.

PMID:
11714865
18.

Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity.

Hu JJ, Smith TR, Miller MS, Mohrenweiser HW, Golden A, Case LD.

Carcinogenesis. 2001 Jun;22(6):917-22.

PMID:
11375899
19.

Genetic variability in susceptibility and response to toxicants.

Miller MC 3rd, Mohrenweiser HW, Bell DA.

Toxicol Lett. 2001 Mar 31;120(1-3):269-80. Review.

PMID:
11323185
20.

Polymorphisms in the DNA repair gene XRCC1 and breast cancer.

Duell EJ, Millikan RC, Pittman GS, Winkel S, Lunn RM, Tse CK, Eaton A, Mohrenweiser HW, Newman B, Bell DA.

Cancer Epidemiol Biomarkers Prev. 2001 Mar;10(3):217-22.

21.

Uncertainty of response to ionizing radiation due to genotype: potential role for variation in DNA repair genes.

Mohrenweiser HW, Jones IM.

Radiat Res. 2000 Dec;154(6):722-3;discussion 723-4. No abstract available.

PMID:
11187011
22.

Functional characterization of Ape1 variants identified in the human population.

Hadi MZ, Coleman MA, Fidelis K, Mohrenweiser HW, Wilson DM 3rd.

Nucleic Acids Res. 2000 Oct 15;28(20):3871-9.

23.

Production and processing of erythropoietin receptor transcripts in brain.

Chin K, Yu X, Beleslin-Cokic B, Liu C, Shen K, Mohrenweiser HW, Noguchi CT.

Brain Res Mol Brain Res. 2000 Sep 30;81(1-2):29-42.

PMID:
11000476
24.

Mapping of the chromosome 19 q-arm glioma tumor suppressor gene using fluorescence in situ hybridization and novel microsatellite markers.

Smith JS, Tachibana I, Lee HK, Qian J, Pohl U, Mohrenweiser HW, Borell TJ, Hosek SM, Soderberg CL, von Deimling A, Perry A, Scheithauer BW, Louis DN, Jenkins RB.

Genes Chromosomes Cancer. 2000 Sep;29(1):16-25.

PMID:
10918389
25.
26.

A transcript map of the chromosome 19q-arm glioma tumor suppressor region.

Smith JS, Tachibana I, Pohl U, Lee HK, Thanarajasingam U, Portier BP, Ueki K, Ramaswamy S, Billings SJ, Mohrenweiser HW, Louis DN, Jenkins RB.

Genomics. 2000 Feb 15;64(1):44-50.

PMID:
10708517
27.

EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteins.

Pohl U, Smith JS, Tachibana I, Ueki K, Lee HK, Ramaswamy S, Wu Q, Mohrenweiser HW, Jenkins RB, Louis DN.

Genomics. 2000 Jan 15;63(2):255-62.

PMID:
10673336
28.

A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13.

Servidei S, Capon F, Spinazzola A, Mirabella M, Semprini S, de Rosa G, Gennarelli M, Sangiuolo F, Ricci E, Mohrenweiser HW, Dallapiccola B, Tonali P, Novelli G.

Neurology. 1999 Sep 11;53(4):830-7.

PMID:
10489050
29.

Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene.

Her C, Wood TC, Eichler EE, Mohrenweiser HW, Ramagli LS, Siciliano MJ, Weinshilboum RM.

Genomics. 1998 Nov 1;53(3):284-95.

PMID:
9799594
30.

Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12.

Eichler EE, Hoffman SM, Adamson AA, Gordon LA, McCready P, Lamerdin JE, Mohrenweiser HW.

Genome Res. 1998 Aug;8(8):791-808.

31.
32.
33.

JAK3 maps to human chromosome 19p12 within a cluster of proto-oncogenes and transcription factors.

Hoffman SM, Lai KS, Tomfohrde J, Bowcock A, Gordon LA, Mohrenweiser HW.

Genomics. 1997 Jul 1;43(1):109-11. No abstract available.

PMID:
9226382
34.

Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity.

Eichler EE, Budarf ML, Rocchi M, Deaven LL, Doggett NA, Baldini A, Nelson DL, Mohrenweiser HW.

Hum Mol Genet. 1997 Jul;6(7):991-1002.

PMID:
9215666
35.

ANOVA, a putative astrocytic RNA-binding protein gene that maps to chromosome 19q13.3.

Ueki K, Ramaswamy S, Billings SJ, Mohrenweiser HW, Louis DN.

Neurogenetics. 1997 May;1(1):31-6.

PMID:
10735272
36.

Chromosomal localization to 19q13.3, partial genomic structure and 5' cDNA sequence of the human symplekin gene.

Ueki K, Ramaswamy S, Billings SJ, Mohrenweiser HW, Louis DN.

Somat Cell Mol Genet. 1997 May;23(3):229-31.

PMID:
9330635
37.

Refined deletion mapping of the chromosome 19q glioma tumor suppressor gene to the D19S412-STD interval.

Rosenberg JE, Lisle DK, Burwick JA, Ueki K, von Deimling A, Mohrenweiser HW, Louis DN.

Oncogene. 1996 Dec 5;13(11):2483-5.

PMID:
8957092
38.

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.

Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR.

Cell. 1996 Nov 1;87(3):543-52.

39.

Molecular cloning, genomic organization, and expression of a testicular isoform of hormone-sensitive lipase.

Holst LS, Langin D, Mulder H, Laurell H, Grober J, Bergh A, Mohrenweiser HW, Edgren G, Holm C.

Genomics. 1996 Aug 1;35(3):441-7.

PMID:
8812477
40.

The BAX gene maps to the glioma candidate region at 19q13.3, but is not altered in human gliomas.

Chou D, Miyashita T, Mohrenweiser HW, Ueki K, Kastury K, Druck T, von Deimling A, Huebner K, Reed JC, Louis DN.

Cancer Genet Cytogenet. 1996 Jun;88(2):136-40.

PMID:
8640722
41.

The location of MZF-1 at the telomere of human chromosome 19q makes it vulnerable to degeneration in aging cells.

Hoffman SM, Hromas R, Amemiya C, Mohrenweiser HW.

Leuk Res. 1996 Mar;20(3):281-3.

PMID:
8637224
42.
44.

Organization and evolution of the cytochrome P450 CYP2A-2B-2F subfamily gene cluster on human chromosome 19.

Hoffman SM, Fernandez-Salguero P, Gonzalez FJ, Mohrenweiser HW.

J Mol Evol. 1995 Dec;41(6):894-900.

PMID:
8587134
45.

A 30-Mb metric fluorescence in situ hybridization map of human chromosome 19q.

Gordon LA, Bergmann A, Christensen M, Danganan L, Lee DA, Ashworth LK, Nelson DO, Olsen AS, Mohrenweiser HW, Carrano AV, et al.

Genomics. 1995 Nov 20;30(2):187-94.

PMID:
8586418
46.

Cloning of a highly conserved human protein serine-threonine phosphatase gene from the glioma candidate region on chromosome 19q13.3.

Yong WH, Ueki K, Chou D, Reeves SA, von Deimling A, Gusella JF, Mohrenweiser HW, Buckler AJ, Louis DN.

Genomics. 1995 Sep 20;29(2):533-6.

PMID:
8666404
47.

Chromosome 19q deletions in human gliomas overlap telomeric to D19S219 and may target a 425 kb region centromeric to D19S112.

Yong WH, Chou D, Ueki K, Harsh GR 4th, von Deimling A, Gusella JF, Mohrenweiser HW, Louis DN.

J Neuropathol Exp Neurol. 1995 Sep;54(5):622-6.

PMID:
7666049
48.

The hormone-sensitive lipase (LIPE) gene located on chromosome 19q13.1-->13.2 is not duplicated on 19p13.3.

Laurell H, Grober J, Holst LS, Holm C, Mohrenweiser HW, Langin D.

Int J Obes Relat Metab Disord. 1995 Aug;19(8):590-2.

PMID:
7489032
49.

Molecular analysis of four ENU induced triosephosphate isomerase null mutants in Mus musculus.

Zingg BC, Pretsch W, Mohrenweiser HW.

Mutat Res. 1995 May;328(2):163-73.

PMID:
7739600
50.

Dehydroepiandrosterone sulfotransferase gene (STD): localization to human chromosome band 19q13.3.

Otterness DM, Mohrenweiser HW, Brandriff BF, Weinshilboum RM.

Cytogenet Cell Genet. 1995;70(1-2):45-7.

PMID:
7736787

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