151 related articles for article (PubMed ID: 15461631)
1. Hemojuvelin (HJV) mutations in persons of European, African-American and Asian ancestry with adult onset haemochromatosis.
Lee PL; Barton JC; Brandhagen D; Beutler E
Br J Haematol; 2004 Oct; 127(2):224-9. PubMed ID: 15461631
[TBL] [Abstract][Full Text] [Related]
2. Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population.
Barton JC; Rivers CA; Niyongere S; Bohannon SB; Acton RT
BMC Med Genet; 2004 Dec; 5():29. PubMed ID: 15610558
[TBL] [Abstract][Full Text] [Related]
3. Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patient.
Daraio F; Ryan E; Gleeson F; Roetto A; Crowe J; Camaschella C
Blood Cells Mol Dis; 2005; 35(2):174-6. PubMed ID: 15967692
[TBL] [Abstract][Full Text] [Related]
4. Genetic abnormalities and juvenile hemochromatosis: mutations of the HJV gene encoding hemojuvelin.
Lee PL; Beutler E; Rao SV; Barton JC
Blood; 2004 Jun; 103(12):4669-71. PubMed ID: 14982867
[TBL] [Abstract][Full Text] [Related]
5. Non-
Lv T; Zhang W; Xu A; Li Y; Zhou D; Zhang B; Li X; Zhao X; Wang Y; Wang X; Duan W; Wang Q; Xu H; Zheng J; Zhao R; Zhu L; Dong Y; Lu L; Chen Y; Long J; Zheng S; Wang W; You H; Jia J; Ou X; Huang J
J Med Genet; 2018 Oct; 55(10):650-660. PubMed ID: 30166352
[TBL] [Abstract][Full Text] [Related]
6. Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report.
Militaru MS; Popp RA; Trifa AP
J Gastrointestin Liver Dis; 2010 Jun; 19(2):191-3. PubMed ID: 20593054
[TBL] [Abstract][Full Text] [Related]
7. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
Santos PC; Cançado RD; Pereira AC; Schettert IT; Soares RA; Pagliusi RA; Hirata RD; Hirata MH; Teixeira AC; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
Blood Cells Mol Dis; 2011 Apr; 46(4):302-7. PubMed ID: 21411349
[TBL] [Abstract][Full Text] [Related]
8. Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes.
Pietrangelo A; Caleffi A; Henrion J; Ferrara F; Corradini E; Kulaksiz H; Stremmel W; Andreone P; Garuti C
Gastroenterology; 2005 Feb; 128(2):470-9. PubMed ID: 15685557
[TBL] [Abstract][Full Text] [Related]
9. The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype.
Le Gac G; Scotet V; Ka C; Gourlaouen I; Bryckaert L; Jacolot S; Mura C; Férec C
Hum Mol Genet; 2004 Sep; 13(17):1913-8. PubMed ID: 15254010
[TBL] [Abstract][Full Text] [Related]
10. Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis.
Lanzara C; Roetto A; Daraio F; Rivard S; Ficarella R; Simard H; Cox TM; Cazzola M; Piperno A; Gimenez-Roqueplo AP; Grammatico P; Volinia S; Gasparini P; Camaschella C
Blood; 2004 Jun; 103(11):4317-21. PubMed ID: 14982873
[TBL] [Abstract][Full Text] [Related]
11. Early age-of-onset iron overload and homozygosity for the novel hemojuvelin mutation HJV R54X (exon 3; c.160A-->T) in an African American male of West Indies descent.
Murugan RC; Lee PL; Kalavar MR; Barton JC
Clin Genet; 2008 Jul; 74(1):88-92. PubMed ID: 18492090
[TBL] [Abstract][Full Text] [Related]
12. Identification of a novel mutation (C321X) in HJV.
Huang FW; Rubio-Aliaga I; Kushner JP; Andrews NC; Fleming MD
Blood; 2004 Oct; 104(7):2176-7. PubMed ID: 15138164
[TBL] [Abstract][Full Text] [Related]
13. HJV gene mutations in European patients with juvenile hemochromatosis.
Gehrke SG; Pietrangelo A; Kascák M; Braner A; Eisold M; Kulaksiz H; Herrmann T; Hebling U; Bents K; Gugler R; Stremmel W
Clin Genet; 2005 May; 67(5):425-8. PubMed ID: 15811010
[TBL] [Abstract][Full Text] [Related]
14. Juvenile hemochromatosis associated with heterozygosity for novel hemojuvelin mutations and with unknown cofactors.
Pelusi S; Rametta R; Della Corte C; Congia R; Dongiovanni P; Pulixi EA; Fargion S; Fracanzani AL; Nobili V; Valenti L
Ann Hepatol; 2014; 13(5):568-71. PubMed ID: 25152992
[TBL] [Abstract][Full Text] [Related]
15. Adult onset hereditary hemochromatosis is associated with a novel recurrent Hemojuvelin (HJV) gene mutation in north Indians.
Dhillon BK; Chopra G; Jamwal M; Chandak GR; Duseja A; Malhotra P; Chawla YK; Garewal G; Das R
Blood Cells Mol Dis; 2018 Nov; 73():14-21. PubMed ID: 30195625
[TBL] [Abstract][Full Text] [Related]
16. Juvenile hemochromatosis caused by a novel combination of hemojuvelin G320V/R176C mutations in a 5-year old girl.
Aguilar-Martinez P; Lok CY; Cunat S; Cadet E; Robson K; Rochette J
Haematologica; 2007 Mar; 92(3):421-2. PubMed ID: 17339196
[TBL] [Abstract][Full Text] [Related]
17. Interaction of hemojuvelin with neogenin results in iron accumulation in human embryonic kidney 293 cells.
Zhang AS; West AP; Wyman AE; Bjorkman PJ; Enns CA
J Biol Chem; 2005 Oct; 280(40):33885-94. PubMed ID: 16103117
[TBL] [Abstract][Full Text] [Related]
18. Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele.
Biasiotto G; Roetto A; Daraio F; Polotti A; Gerardi GM; Girelli D; Cremonesi L; Arosio P; Camaschella C
Blood Cells Mol Dis; 2004; 33(3):338-43. PubMed ID: 15528154
[TBL] [Abstract][Full Text] [Related]
19. Hereditary hemochromatosis in north-eastern Romania.
Voicu PM; Cojocariu C; Petrescu-Dănilă E; Stanciu C; Covic M; Rusu M; Trifan A
Rev Med Chir Soc Med Nat Iasi; 2010; 114(4):982-7. PubMed ID: 21495455
[TBL] [Abstract][Full Text] [Related]
20. Recent advances in understanding haemochromatosis: a transition state.
Robson KJ; Merryweather-Clarke AT; Cadet E; Viprakasit V; Zaahl MG; Pointon JJ; Weatherall DJ; Rochette J
J Med Genet; 2004 Oct; 41(10):721-30. PubMed ID: 15466004
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]