These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

51 related articles for article (PubMed ID: 10738001)

  • 1. A novel polymorphism (219G>A) in the transferrin receptor gene.
    Meregalli M; Corbetta N; Pellagatti A; Martinez di Montemuros F; Tavazzi D; Fargion S; Sampietro M
    Hum Mutat; 2000 Apr; 15(4):389. PubMed ID: 10738001
    [No Abstract]   [Full Text] [Related]  

  • 2. Molecular analysis of the TFR2 gene: report of a novel polymorphism (1878C>T).
    Meregalli M; Pellagatti A; Bissolotti E; Fracanzani AL; Fargion S; Sampietro M
    Hum Mutat; 2000 Dec; 16(6):532. PubMed ID: 11102989
    [No Abstract]   [Full Text] [Related]  

  • 3. New TFR2 mutations in young Italian patients with hemochromatosis.
    Biasiotto G; Camaschella C; Forni GL; Polotti A; Zecchina G; Arosio P
    Haematologica; 2008 Feb; 93(2):309-10. PubMed ID: 18245657
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation screening of the muscarinic M(2) and M(3) receptor genes in normal and asthmatic subjects.
    Fenech AG; Ebejer MJ; Felice AE; Ellul-Micallef R; Hall IP
    Br J Pharmacol; 2001 May; 133(1):43-8. PubMed ID: 11325793
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Soluble transferrin receptor and mutations in hemochromatosis and transferrin genes in a general Catalan population.
    Bérez V; Camps J; Arija V; Aranda N; Fernández-Ballart J; Vilella E; Figuera L; Ferré N; Joven J
    Clin Chim Acta; 2005 Mar; 353(1-2):205-8. PubMed ID: 15698609
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Commentary: mutations of transferrin receptor 2 (Trf-2) and iron storage disease.
    Beutler E
    Blood Cells Mol Dis; 2001; 27(1):294-5. PubMed ID: 11358391
    [No Abstract]   [Full Text] [Related]  

  • 7. Two novel mutations, L490R and V561X, in transferrin receptor 2 in Japanese patients with hemochromatosis.
    Bergamaschi G
    Haematologica; 2005 Mar; 90(3):289A. PubMed ID: 15749651
    [No Abstract]   [Full Text] [Related]  

  • 8. Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).
    Lamoril J; Andant C; Gouya L; Malonova E; Grandchamp B; Martásek P; Deybac JC; Puy H
    Cell Mol Biol (Noisy-le-grand); 2002 Feb; 48(1):33-41. PubMed ID: 11929045
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.
    Koyama C; Wakusawa S; Hayashi H; Suzuki R; Yano M; Yoshioka K; Kozuru M; Takayamam Y; Okada T; Mabuchi H
    Haematologica; 2005 Mar; 90(3):302-7. PubMed ID: 15749661
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human GABA(B) receptor 1 gene: eight novel sequence variants.
    Hisama FM; Gruen JR; Choi J; Huseinovic M; Grigorenko EL; Pauls D; Mattson RH; Gelernter J; Wood FB; Goei VL
    Hum Mutat; 2001 Apr; 17(4):349-50. PubMed ID: 11295833
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin.
    Lee PL; Gelbart T; West C; Halloran C; Felitti V; Beutler E
    Blood Cells Mol Dis; 2001; 27(5):783-802. PubMed ID: 11783942
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.
    Morcuende JA; Minhas R; Dolan L; Stevens J; Beck J; Wang K; Weinstein SL; Sheffield V
    Spine (Phila Pa 1976); 2003 Sep; 28(17):2025-8; discussion 2029. PubMed ID: 12973153
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genomewide linkage analysis of soluble transferrin receptor plasma levels.
    Remacha AF; Souto JC; Soria JM; Buil A; Sardà MP; Lathrop M; Blangero J; Almasy L; Fontcuberta J
    Ann Hematol; 2006 Jan; 85(1):25-8. PubMed ID: 16132911
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent.
    Le Gac G; Mons F; Jacolot S; Scotet V; Férec C; Frébourg T
    Br J Haematol; 2004 Jun; 125(5):674-8. PubMed ID: 15147384
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Structure and methylation state of the human transferrin receptor gene: preliminary analysis on tumor cell lines, primary tumors and some normal tissues.
    Piva R; Barbieri R; Mischiati C; Feriotto G; Nastruzzi C; Volinia S; Gambari R
    Boll Soc Ital Biol Sper; 1987 Apr; 63(4):311-5. PubMed ID: 2896006
    [No Abstract]   [Full Text] [Related]  

  • 16. Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.
    Majore S; Milano F; Binni F; Stuppia L; Cerrone A; Tafuri A; De Bernardo C; Palka G; Grammatico P
    Haematologica; 2006 Aug; 91(8 Suppl):ECR33. PubMed ID: 16923517
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Detecting the DNA polymorphism of human complement component C8A by PCR-SSCP analysis].
    Yang ZH; Zhang L; Zhou B; Wang C; Jia J
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2006 May; 37(3):471-3. PubMed ID: 16761437
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Is the CACNA1A gene involved in familial migraine with aura?
    Brugnoni R; Leone M; Rigamonti A; Moranduzzo E; Cornelio F; Mantegazza R; Bussone G
    Neurol Sci; 2002 Apr; 23(1):1-5. PubMed ID: 12111613
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent.
    Gérolami V; Le Gac G; Mercier L; Nezri M; Bergé-Lefranc JL; Férec C
    Haematologica; 2008 May; 93(5):e45-6. PubMed ID: 18450729
    [No Abstract]   [Full Text] [Related]  

  • 20. Molecular and cellular characterization of transferrin receptor 2.
    Subramaniam VN; Summerville L; Wallace DF
    Cell Biochem Biophys; 2002; 36(2-3):235-9. PubMed ID: 12139409
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.