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Results: 1 to 20 of 93

1.

What my genome told me--and what it didn't.

Petsko GA.

Genome Biol. 2009;10(6):108. doi: 10.1186/gb-2009-10-6-108. Epub 2009 Jun 29.

PMID:
19591645
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

HFE gene and hemochromatosis.

Anderson GJ, Ramm GA, Subramaniam VN, Powell LW.

J Gastroenterol Hepatol. 2004 Jun;19(6):712. No abstract available.

PMID:
15151632
[PubMed - indexed for MEDLINE]
3.

Low clinical penetrance of homozygosity for HFE C282Y: implications for genetic testing?

Födinger M, Sunder-Plassmann G.

Eur J Clin Invest. 2003 Sep;33(9):737-9. No abstract available.

PMID:
12925029
[PubMed - indexed for MEDLINE]
4.

[Hemochromatosis, a public health problem].

Aguilar Martinez P.

Soins. 2007 Jun;(716):34-5. French. No abstract available.

PMID:
17718029
[PubMed - indexed for MEDLINE]
5.

Can defects in transferrin receptor 2 and hereditary hemochromatosis genes account for iron overload in HbH disease?

Chan V, Wong MS, Ooi C, Chen FE, Chim CS, Liang RH, Todd D, Chan TK.

Blood Cells Mol Dis. 2003 Jan-Feb;30(1):107-11.

PMID:
12667993
[PubMed - indexed for MEDLINE]
6.

[Mutations in the HFE gene in patients with rheumatic diseases].

Půtová I, Cimburová M, Jarosová K, Vencovský J, Horák J.

Cas Lek Cesk. 2005;144(6):391-7; discussion 397-8. Czech.

PMID:
16047841
[PubMed - indexed for MEDLINE]
7.

Letter by Sullivan regarding article, "HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: the hemochromatosis and iron overload screening study".

Sullivan JL.

Circ Cardiovasc Genet. 2009 Jun;2(3):e1. doi: 10.1161/CIRCGENETICS.109.863860. No abstract available.

PMID:
20031587
[PubMed - indexed for MEDLINE]
Free Article
8.

Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.

Shi Z, Johnstone D, Talseth-Palmer BA, Evans TJ, Spigelman AD, Groombridge C, Milward EA, Olynyk JK, Suchy J, Kurzawski G, Lubinski J, Scott RJ.

Int J Cancer. 2009 Jul 1;125(1):78-83. doi: 10.1002/ijc.24304.

PMID:
19291797
[PubMed - indexed for MEDLINE]
9.

Genetic screening for hemochromatosis: a cautionary tale.

Starczynski J, Hooper L, Ali N, Hill M, Fegan C, Pratt G.

Clin Chem. 2005 Mar;51(3):673. No abstract available.

PMID:
15738526
[PubMed - indexed for MEDLINE]
Free Article
10.

The complete genome of an individual by massively parallel DNA sequencing.

Wheeler DA, Srinivasan M, Egholm M, Shen Y, Chen L, McGuire A, He W, Chen YJ, Makhijani V, Roth GT, Gomes X, Tartaro K, Niazi F, Turcotte CL, Irzyk GP, Lupski JR, Chinault C, Song XZ, Liu Y, Yuan Y, Nazareth L, Qin X, Muzny DM, Margulies M, Weinstock GM, Gibbs RA, Rothberg JM.

Nature. 2008 Apr 17;452(7189):872-6. doi: 10.1038/nature06884.

PMID:
18421352
[PubMed - indexed for MEDLINE]
11.

Frequency and spectrum of hemochromatosis mutations in Tunisia.

Zorai A, Harteveld CL, Rachdi R, Dellagi K, Abbes S, Delbini P, Giordano PC.

Hematol J. 2003;4(6):433-5.

PMID:
14671616
[PubMed - indexed for MEDLINE]
12.

Advances in genome studies: The PAG 2010 conference.

Appels R, Barrerro R, Keeble G, Bellgard M.

Funct Integr Genomics. 2010 Mar;10(1):1-9. doi: 10.1007/s10142-010-0164-5.

PMID:
20182762
[PubMed - indexed for MEDLINE]
13.

The significance of the 187G (H63D) mutation in hemochromatosis.

Beutler E.

Am J Hum Genet. 1997 Sep;61(3):762-4. No abstract available.

PMID:
9326341
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Bioelectronic detection of point mutations using discrimination of the H63D polymorphism of the Hfe gene as a model.

Umek RM, Lin SS, Chen Yp Y, Irvine B, Paulluconi G, Chan V, Chong Y, Cheung L, Vielmetter J, Farkas DH.

Mol Diagn. 2000 Dec;5(4):321-8.

PMID:
11172496
[PubMed - indexed for MEDLINE]
15.

Liver disorder and the HFE locus.

Stewart SF, Day CP.

QJM. 2001 Sep;94(9):453-6. No abstract available.

PMID:
11528007
[PubMed - indexed for MEDLINE]
Free Article
16.

Detection of an unusual combination of mutations in the HFE gene for hemochromatosis.

Thorstensen K, Asberg A, Kvitland M, Svaasand E, Hveem K, Bjerve KS.

Genet Test. 2000;4(4):371-6.

PMID:
11216661
[PubMed - indexed for MEDLINE]
17.

High-performance genetic analysis using microfabricated capillary array electrophoresis microplates.

Medintz IL, Paegel BM, Blazej RG, Emrich CA, Berti L, Scherer JR, Mathies RA.

Electrophoresis. 2001 Oct;22(18):3845-56. Review.

PMID:
11700713
[PubMed - indexed for MEDLINE]
18.

Evolutionary genetics. Jumbled DNA separates chimps and humans.

Pennisi E.

Science. 2002 Oct 25;298(5594):719-21. No abstract available.

PMID:
12399553
[PubMed - indexed for MEDLINE]
19.

Juvenile hemochromatosis due to homozygosity for the G320V mutation in the HJV gene with fatal outcome.

Brakensiek K, Fegbeutel C, Mälzer M, Strüber M, Kreipe H, Stuhrmann M.

Clin Genet. 2009 Nov;76(5):493-5. doi: 10.1111/j.1399-0004.2009.01261.x. Epub 2009 Sep 30. No abstract available.

PMID:
19796184
[PubMed - indexed for MEDLINE]
20.

Cardiac hemochromatosis in an HFE His63Asp (187C->G) heterozygote.

Winer D, Silversides C, Israel N, Rinne C, Chang WS, Butany J.

Can J Cardiol. 2004 Aug;20(10):971-2. No abstract available.

PMID:
15332145
[PubMed - indexed for MEDLINE]

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