121 related articles for article (PubMed ID: 3348218)
1. Introduction and expression of the human Bs-globin gene in transgenic mice.
Rubin EM; Lu RH; Cooper S; Mohandas N; Kan YW
Am J Hum Genet; 1988 Apr; 42(4):585-91. PubMed ID: 3348218
[TBL] [Abstract][Full Text] [Related]
2. High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequences.
Fabry ME; Nagel RL; Pachnis A; Suzuka SM; Costantini F
Proc Natl Acad Sci U S A; 1992 Dec; 89(24):12150-4. PubMed ID: 1465454
[TBL] [Abstract][Full Text] [Related]
3. Effect of human beta (s)-globin chains on cellular properties of red cells from beta-thalassemic mice.
Rubin EM; Kan YW; Mohandas N
J Clin Invest; 1988 Sep; 82(3):1129-33. PubMed ID: 3417869
[TBL] [Abstract][Full Text] [Related]
4. Human sickle hemoglobin in transgenic mice.
Ryan TM; Townes TM; Reilly MP; Asakura T; Palmiter RD; Brinster RL; Behringer RR
Science; 1990 Feb; 247(4942):566-8. PubMed ID: 2154033
[TBL] [Abstract][Full Text] [Related]
5. Towards a transgenic mouse model of sickle cell disease: hemoglobin SAD.
Trudel M; Saadane N; Garel MC; Bardakdjian-Michau J; Blouquit Y; Guerquin-Kern JL; Rouyer-Fessard P; Vidaud D; Pachnis A; Roméo PH
EMBO J; 1991 Nov; 10(11):3157-65. PubMed ID: 1915288
[TBL] [Abstract][Full Text] [Related]
6. Mouse model of human beta zero thalassemia: targeted deletion of the mouse beta maj- and beta min-globin genes in embryonic stem cells.
Ciavatta DJ; Ryan TM; Farmer SC; Townes TM
Proc Natl Acad Sci U S A; 1995 Sep; 92(20):9259-63. PubMed ID: 7568113
[TBL] [Abstract][Full Text] [Related]
7. A human embryonic hemoglobin inhibits Hb S polymerization in vitro and restores a normal phenotype to mouse models of sickle cell disease.
He Z; Russell JE
Proc Natl Acad Sci U S A; 2002 Aug; 99(16):10635-40. PubMed ID: 12124399
[TBL] [Abstract][Full Text] [Related]
8. Pathophysiology of a sickle cell trait mouse model: human alpha(beta)(S) transgenes with one mouse beta-globin allele.
Noguchi CT; Gladwin M; Diwan B; Merciris P; Smith R; Yu X; Buzard G; Fitzhugh A; Keefer LK; Schechter AN; Mohandas N
Blood Cells Mol Dis; 2001; 27(6):971-7. PubMed ID: 11831863
[TBL] [Abstract][Full Text] [Related]
9. Hypoxia-induced in vivo sickling of transgenic mouse red cells.
Rubin EM; Witkowska HE; Spangler E; Curtin P; Lubin BH; Mohandas N; Clift SM
J Clin Invest; 1991 Feb; 87(2):639-47. PubMed ID: 1991848
[TBL] [Abstract][Full Text] [Related]
10. A second generation transgenic mouse model expressing both hemoglobin S (HbS) and HbS-Antilles results in increased phenotypic severity.
Fabry ME; Sengupta A; Suzuka SM; Costantini F; Rubin EM; Hofrichter J; Christoph G; Manci E; Culberson D; Factor SM; Nagel RL
Blood; 1995 Sep; 86(6):2419-28. PubMed ID: 7662990
[TBL] [Abstract][Full Text] [Related]
11. Transgenic knockout mice exclusively expressing human hemoglobin S after transfer of a 240-kb betas-globin yeast artificial chromosome: A mouse model of sickle cell anemia.
Chang JC; Lu R; Lin C; Xu SM; Kan YW; Porcu S; Carlson E; Kitamura M; Yang S; Flebbe-Rehwaldt L; Gaensler KM
Proc Natl Acad Sci U S A; 1998 Dec; 95(25):14886-90. PubMed ID: 9843985
[TBL] [Abstract][Full Text] [Related]
12. Knockout-transgenic mouse model of sickle cell disease.
Ryan TM; Ciavatta DJ; Townes TM
Science; 1997 Oct; 278(5339):873-6. PubMed ID: 9346487
[TBL] [Abstract][Full Text] [Related]
13. A recombinant human hemoglobin with anti-sickling properties greater than fetal hemoglobin.
Levasseur DN; Ryan TM; Reilly MP; McCune SL; Asakura T; Townes TM
J Biol Chem; 2004 Jun; 279(26):27518-24. PubMed ID: 15084588
[TBL] [Abstract][Full Text] [Related]
14. Recombinant human hemoglobins designed for gene therapy of sickle cell disease.
McCune SL; Reilly MP; Chomo MJ; Asakura T; Townes TM
Proc Natl Acad Sci U S A; 1994 Oct; 91(21):9852-6. PubMed ID: 7937904
[TBL] [Abstract][Full Text] [Related]
15. DNase I super-hypersensitive sites direct high level erythroid expression of human alpha-, beta- and beta s- globin genes in transgenic mice.
Townes TM; Ryan TM; Behringer RR; Palmiter RD; Brinster RL
Prog Clin Biol Res; 1989; 316A():47-61. PubMed ID: 2594817
[No Abstract] [Full Text] [Related]
16. Use of a new mouse beta-globin haplotype (Hbbs2) to study hemoglobin expression during development.
Wawrzyniak CJ; Popp RA
Dev Biol; 1985 Dec; 112(2):477-84. PubMed ID: 4076548
[TBL] [Abstract][Full Text] [Related]
17. High oxygen environment during pregnancy rescues sickle cell anemia mice from prenatal death.
Ye L; Chang JC; Lu R; Kan YW
Blood Cells Mol Dis; 2008; 41(1):67-72. PubMed ID: 18207438
[TBL] [Abstract][Full Text] [Related]
18. High expression of human beta S- and alpha-globins in transgenic mice: erythrocyte abnormalities, organ damage, and the effect of hypoxia.
Fabry ME; Costantini F; Pachnis A; Suzuka SM; Bank N; Aynedjian HS; Factor SM; Nagel RL
Proc Natl Acad Sci U S A; 1992 Dec; 89(24):12155-9. PubMed ID: 1465455
[TBL] [Abstract][Full Text] [Related]
19. Novel metabolism of several beta zero-thalassemic beta-globin mRNAs in the erythroid tissues of transgenic mice.
Lim S; Mullins JJ; Chen CM; Gross KW; Maquat LE
EMBO J; 1989 Sep; 8(9):2613-9. PubMed ID: 2573525
[TBL] [Abstract][Full Text] [Related]
20. Transgenic knockout mice with exclusively human sickle hemoglobin and sickle cell disease.
Pászty C; Brion CM; Manci E; Witkowska HE; Stevens ME; Mohandas N; Rubin EM
Science; 1997 Oct; 278(5339):876-8. PubMed ID: 9346488
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]