Similar articles for PMID: 3467311

Year	Number of Results
1924	1
1929	1
1966	1
1971	2
1972	1
1973	5
1974	5
1975	10
1976	9
1977	18
1978	6
1979	11
1980	9
1981	13
1982	12
1983	7
1984	7
1985	3
1986	12
1987	10
1988	5
1989	3
1990	7
1991	5
1992	2
1993	6
1994	9
1995	4
1996	8
1997	7
1998	6
1999	6
2001	2
2002	8
2003	1
2004	5
2006	3
2007	2
2008	1
2009	2
2010	6
2011	2
2012	5
2013	2
2014	1
2015	4
2016	5
2017	1
2018	3
2019	3
2020	6
2021	5
2022	7
2023	2
2024	0

1

Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes.

Monplaisir N, Merault G, Poyart C, Rhoda MD, Craescu C, Vidaud M, Galacteros F, Blouquit Y, Rosa J. Monplaisir N, et al. Proc Natl Acad Sci U S A. 1986 Dec;83(24):9363-7. doi: 10.1073/pnas.83.24.9363. Proc Natl Acad Sci U S A. 1986. PMID: 3467311 Free PMC article.

2

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. Fabry ME, et al. Blood. 1995 Sep 15;86(6):2419-28. Blood. 1995. PMID: 7662990 Free article.

3

A transgenic mouse model of hemoglobin S Antilles disease.

Popp RA, Popp DM, Shinpock SG, Yang MY, Mural JG, Aguinaga MP, Kopsombut P, Roa PD, Turner EA, Rubin EM. Popp RA, et al. Blood. 1997 Jun 1;89(11):4204-12. Blood. 1997. PMID: 9166865 Free article.

4

Haemoglobin alpha 2 beta 2 23Val----Ile produced in Escherichia coli facilitates Hb S polymerization.

Pagnier J, Baudin-Chich V, Lacaze N, Bohn B, Poyart C. Pagnier J, et al. Br J Haematol. 1990 Apr;74(4):531-4. doi: 10.1111/j.1365-2141.1990.tb06346.x. Br J Haematol. 1990. PMID: 2189492

5

A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry).

Cohen-Solal M, Préhu C, Wajcman H, Poyart C, Bardakdjian-Michau J, Kister J, Promé D, Valentin C, Bachir D, Galactéros F. Cohen-Solal M, et al. Br J Haematol. 1998 Dec;103(4):950-6. doi: 10.1046/j.1365-2141.1998.01094.x. Br J Haematol. 1998. PMID: 9886305 Free article.

6

HbS-oman heterozygote: a new dominant sickle syndrome.

Nagel RL, Daar S, Romero JR, Suzuka SM, Gravell D, Bouhassira E, Schwartz RS, Fabry ME, Krishnamoorthy R. Nagel RL, et al. Blood. 1998 Dec 1;92(11):4375-82. Blood. 1998. PMID: 9834244 Free article.

7

A novel sickle hemoglobin: hemoglobin S-south end.

Luo HY, Adewoye AH, Eung SH, Skelton TP, Quillen K, McMahon L, Steinberg MH, Chui DH. Luo HY, et al. J Pediatr Hematol Oncol. 2004 Nov;26(11):773-6. doi: 10.1097/00043426-200411000-00019. J Pediatr Hematol Oncol. 2004. PMID: 15543018

8

Hypoxia-induced in vivo sickling of transgenic mouse red cells.

Rubin EM, Witkowska HE, Spangler E, Curtin P, Lubin BH, Mohandas N, Clift SM. Rubin EM, et al. J Clin Invest. 1991 Feb;87(2):639-47. doi: 10.1172/JCI115041. J Clin Invest. 1991. PMID: 1991848 Free PMC article.

9

Hb S-São Paulo: a new sickling hemoglobin with stable polymers and decreased oxygen affinity.

Jorge SE, Petruk AA, Kimura EM, Oliveira DM, Caire L, Suemasu CN, Silveira PA, Albuquerque DM, Costa FF, Skaf MS, Martínez L, Sonati Mde F. Jorge SE, et al. Arch Biochem Biophys. 2012 Mar 1;519(1):23-31. doi: 10.1016/j.abb.2012.01.001. Epub 2012 Jan 8. Arch Biochem Biophys. 2012. PMID: 22244832 Free article.

10

Recombinant human hemoglobins designed for gene therapy of sickle cell disease.

McCune SL, Reilly MP, Chomo MJ, Asakura T, Townes TM. McCune SL, et al. Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9852-6. doi: 10.1073/pnas.91.21.9852. Proc Natl Acad Sci U S A. 1994. PMID: 7937904 Free PMC article.

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