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Journal Abstract Search
141 related items for PubMed ID: 9107525
1. Molecular insights into the Rh protein family and associated antigens. Huang CH. Curr Opin Hematol; 1997 Mar; 4(2):94-103. PubMed ID: 9107525 [Abstract] [Full Text] [Related]
2. Defining the Rh blood group antigens. Biochemistry and molecular genetics. Cartron JP. Blood Rev; 1994 Dec; 8(4):199-212. PubMed ID: 7888828 [Abstract] [Full Text] [Related]
3. The human Rh50 glycoprotein gene. Structural organization and associated splicing defect resulting in Rh(null) disease. Huang CH. J Biol Chem; 1998 Jan 23; 273(4):2207-13. PubMed ID: 9442063 [Abstract] [Full Text] [Related]
4. Expression analysis of human Rhesus blood group antigens by gene transduction into erythroid and non-erythroid cells. Iwamoto S, Yamasaki M, Kawano M, Okuda H, Omi T, Takahashi J, Tani Y, Omine M, Kajii E. Int J Hematol; 1998 Oct 23; 68(3):257-68. PubMed ID: 9846010 [Abstract] [Full Text] [Related]
5. Identification of 5' flanking sequence of RH50 gene and the core region for erythroid-specific expression. Iwamoto S, Omi T, Yamasaki M, Okuda H, Kawano M, Kajii E. Biochem Biophys Res Commun; 1998 Feb 04; 243(1):233-40. PubMed ID: 9473510 [Abstract] [Full Text] [Related]
6. Molecular biology and genetics of the Rh blood group system. Huang CH, Liu PZ, Cheng JG. Semin Hematol; 2000 Apr 04; 37(2):150-65. PubMed ID: 10791884 [Abstract] [Full Text] [Related]
7. Advance in the Rh blood group system. Kajii E. Nihon Hoigaku Zasshi; 1998 Feb 04; 52(1):1-18. PubMed ID: 9591398 [Abstract] [Full Text] [Related]
8. The members of the RH gene family (RH50 and RH30) followed different evolutionary pathways. Matassi G, Chérif-Zahar B, Pesole G, Raynal V, Cartron JP. J Mol Evol; 1999 Feb 04; 48(2):151-9. PubMed ID: 9929383 [Abstract] [Full Text] [Related]
9. Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression. Ridgwell K, Spurr NK, Laguda B, MacGeoch C, Avent ND, Tanner MJ. Biochem J; 1992 Oct 01; 287 ( Pt 1)(Pt 1):223-8. PubMed ID: 1417776 [Abstract] [Full Text] [Related]
10. Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency. Cherif-Zahar B, Raynal V, Gane P, Mattei MG, Bailly P, Gibbs B, Colin Y, Cartron JP. Nat Genet; 1996 Feb 01; 12(2):168-73. PubMed ID: 8563755 [Abstract] [Full Text] [Related]
11. Rhmod syndrome: a family study of the translation-initiator mutation in the Rh50 glycoprotein gene. Huang C, Cheng GJ, Reid ME, Chen Y. Am J Hum Genet; 1999 Jan 01; 64(1):108-17. PubMed ID: 9915949 [Abstract] [Full Text] [Related]
12. Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment. Huang CH, Liu Z, Cheng G, Chen Y. Blood; 1998 Sep 01; 92(5):1776-84. PubMed ID: 9716608 [Abstract] [Full Text] [Related]
13. A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type. Hyland CA, Chérif-Zahar B, Cowley N, Raynal V, Parkes J, Saul A, Cartron JP. Blood; 1998 Feb 15; 91(4):1458-63. PubMed ID: 9454778 [Abstract] [Full Text] [Related]
14. Biochemical aspects of the blood group Rh (rhesus) antigens. Anstee DJ, Tanner MJ. Baillieres Clin Haematol; 1993 Jun 15; 6(2):401-22. PubMed ID: 8043932 [Abstract] [Full Text] [Related]
15. Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background. Huang CH, Chen Y, Reid ME, Seidl C. Blood; 1998 Jul 15; 92(2):664-71. PubMed ID: 9657769 [Abstract] [Full Text] [Related]
16. Expression of Rh30 and Rh-related glycoproteins during erythroid differentiation in a two-phase liquid culture system. Suyama K, Li H, Zhu A. Transfusion; 2000 Feb 15; 40(2):214-21. PubMed ID: 10686006 [Abstract] [Full Text] [Related]
17. [Molecular approaches to the Rh blood group system]. Kajii E. Nihon Hoigaku Zasshi; 2006 Oct 15; 60(2):110-9. PubMed ID: 17134012 [Abstract] [Full Text] [Related]
18. RH blood group system and molecular basis of Rh-deficiency. Cartron JP. Baillieres Best Pract Res Clin Haematol; 1999 Dec 15; 12(4):655-89. PubMed ID: 10895258 [Abstract] [Full Text] [Related]
19. Rh-deficiency of the regulator type caused by splicing mutations in the human RH50 gene. Chérif-Zahar B, Matassi G, Raynal V, Gane P, Delaunay J, Arrizabalaga B, Cartron JP. Blood; 1998 Oct 01; 92(7):2535-40. PubMed ID: 9746795 [Abstract] [Full Text] [Related]
20. Molecular basis of the rare gene complex, DIVa(C)-, which encodes four low-prevalence antigens in the Rh blood group system. Hipsky CH, Hue-Roye K, Lomas-Francis C, Huang CH, Reid ME. Vox Sang; 2012 Feb 01; 102(2):167-70. PubMed ID: 21729099 [Abstract] [Full Text] [Related] Page: [Next] [New Search]