Steinberg MH - Search Results

1

The -87 (C----A) beta(+)-thalassemia mutation in a black family.

Coleman MB, Steinberg MH, Harrell AH, Plonczynski MW, Walker AM, Adams JG 3rd. Coleman MB, et al. Among authors: steinberg mh. Hemoglobin. 1992;16(5):399-401. doi: 10.3109/03630269209005691. Hemoglobin. 1992. PMID: 1428943 No abstract available.

2

Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.

Coleman MB, Adams JG 3rd, Plonczynski MW, Harrell AH, Walker AM, Fairbanks V, Steinberg MH. Coleman MB, et al. Among authors: steinberg mh. Am J Med Sci. 1992 Aug;304(2):73-8. doi: 10.1097/00000441-199208000-00001. Am J Med Sci. 1992. PMID: 1380206

3

Hb Mississippi [beta 44(CD3)Ser----Arg]: a new variant with anomalous properties.

Adams JG 3rd, Morrison WT, Barlow RL, Steinberg MH. Adams JG 3rd, et al. Among authors: steinberg mh. Hemoglobin. 1987;11(5):435-52. doi: 10.3109/03630268708998004. Hemoglobin. 1987. PMID: 3429243

4

G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesis.

Coleman MB, Adams JG 3rd, Steinberg MH, Plonczynski MW, Harrell AH, Castro O, Winter WP. Coleman MB, et al. Among authors: steinberg mh. Am J Hematol. 1993 Feb;42(2):186-90. doi: 10.1002/ajh.2830420209. Am J Hematol. 1993. PMID: 7679879

5

Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).

Coleman MB, Lu ZH, Smith CM 2nd, Adams JG 3rd, Harrell A, Plonczynski M, Steinberg MH. Coleman MB, et al. Among authors: steinberg mh. J Clin Invest. 1995 Feb;95(2):503-9. doi: 10.1172/JCI117691. J Clin Invest. 1995. PMID: 7860732 Free PMC article.

6

Beta-thalassemia in southwestern Iran.

Merat A, Haghshenas M, Pour ZM, Plonczynski MW, Harrell AN, Coleman MB, Steinberg MH. Merat A, et al. Among authors: steinberg mh. Hemoglobin. 1993 Oct;17(5):427-37. doi: 10.3109/03630269308997497. Hemoglobin. 1993. PMID: 8294202

7

Severe Hb S-beta+ thalassemia caused by IVS-I splice site mutations.

Li J, Plonczynski M, Steinberg MH, Kheradpour A, Alter BP. Li J, et al. Among authors: steinberg mh. Hemoglobin. 1998 Jul;22(4):383-6. doi: 10.3109/03630269809071533. Hemoglobin. 1998. PMID: 9730369 No abstract available.

8

Genetic studies suggest a multicentric origin for Hb G-Coushatta [beta22(B4)Glu-->Ala].

Li J, Wilson D, Plonczynski M, Harrell A, Cook CB, Scheer WD, Zeng YT, Coleman MB, Steinberg MH. Li J, et al. Among authors: steinberg mh. Hemoglobin. 1999 Feb;23(1):57-67. doi: 10.3109/03630269908996148. Hemoglobin. 1999. PMID: 10081986

9

Disappearance of the protein of a somatic mutation: a possible example of stem cell inactivation.

Adams JG, Hardy CL, Steinberg MH. Adams JG, et al. Among authors: steinberg mh. Am J Physiol. 1991 Sep;261(3 Pt 1):C448-54. doi: 10.1152/ajpcell.1991.261.3.C448. Am J Physiol. 1991. PMID: 1887872

10

Hemoglobin A2: origin, evolution, and aftermath.

Steinberg MH, Adams JG 3rd. Steinberg MH, et al. Blood. 1991 Nov 1;78(9):2165-77. Blood. 1991. PMID: 1932737 Free article. Review. No abstract available.

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