Huisman TH - Search Results

1

The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C----G substitution at nucleotide -195 of the A gamma-globin gene.

Costa FF, Zago MA, Cheng G, Nechtman JF, Stoming TA, Huisman TH. Costa FF, et al. Among authors: huisman th. Blood. 1990 Nov 1;76(9):1896-7. Blood. 1990. PMID: 2224140 Free article. No abstract available.

2

An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene.

Stoming TA, Stoming GS, Lanclos KD, Fei YJ, Altay C, Kutlar F, Huisman TH. Stoming TA, et al. Among authors: huisman th. Blood. 1989 Jan;73(1):329-33. Blood. 1989. PMID: 2462941 Free article.

3

Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure.

Yang KG, Stoming TA, Fei YJ, Liang S, Wong SC, Masala B, Huang RB, Wei ZP, Huisman TH. Yang KG, et al. Among authors: huisman th. Blood. 1988 May;71(5):1414-7. Blood. 1988. PMID: 2451950 Free article.

4

One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain.

Fei YJ, Stoming TA, Kutlar A, Huisman TH, Stamatoyannopoulos G. Fei YJ, et al. Among authors: huisman th. Blood. 1989 Mar;73(4):1075-7. Blood. 1989. PMID: 2563949 Free article. No abstract available.

5

Distal CCAAT box deletion in the A gamma globin gene of two black adolescents with elevated fetal A gamma globin.

Gilman JG, Mishima N, Wen XJ, Stoming TA, Lobel J, Huisman TH. Gilman JG, et al. Among authors: huisman th. Nucleic Acids Res. 1988 Nov 25;16(22):10635-42. doi: 10.1093/nar/16.22.10635. Nucleic Acids Res. 1988. PMID: 2462713 Free PMC article.

6

Transient chloramphenicol acetyltransferase expression of the G gamma globin gene 5'-flanking regions containing substitutions of C----T at position -158, G----A at position -161, and T----A at position -175 in K562 cells.

Lanclos KD, Michael SK, Gu YC, Howard EF, Stoming TA, Huisman TH. Lanclos KD, et al. Among authors: huisman th. Biochim Biophys Acta. 1989 Jun 1;1008(1):109-12. doi: 10.1016/0167-4781(89)90176-0. Biochim Biophys Acta. 1989. PMID: 2719957

7

The detection of beta-globin gene mutations in beta-thalassemia using oligonucleotide probes and amplified DNA.

Diaz-Chico JC, Yang KG, Yang KY, Efremov DG, Stoming TA, Huisman TH. Diaz-Chico JC, et al. Among authors: huisman th. Biochim Biophys Acta. 1988 Jan 25;949(1):43-8. doi: 10.1016/0167-4781(88)90052-8. Biochim Biophys Acta. 1988. PMID: 2825812

8

Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene.

Gonzalez-Redondo JM, Stoming TA, Kutlar F, Kutlar A, McKie VC, McKie KM, Huisman TH. Gonzalez-Redondo JM, et al. Among authors: huisman th. Br J Haematol. 1989 Jan;71(1):113-7. doi: 10.1111/j.1365-2141.1989.tb06283.x. Br J Haematol. 1989. PMID: 2917118

9

High frequencies of a rearrangement (+ATA; -T) at -530 to the beta-globin gene in different populations indicate the absence of a correlation with a silent beta-thalassemia determinant.

Wong SC, Stoming TA, Efremov GD, Huisman TH. Wong SC, et al. Among authors: huisman th. Hemoglobin. 1989;13(1):1-5. doi: 10.3109/03630268908998048. Hemoglobin. 1989. PMID: 2703362

10

Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.

Yang KG, Kutlar F, George E, Wilson JB, Kutlar A, Stoming TA, Gonzalez-Redondo JM, Huisman TH. Yang KG, et al. Among authors: huisman th. Br J Haematol. 1989 May;72(1):73-80. doi: 10.1111/j.1365-2141.1989.tb07655.x. Br J Haematol. 1989. PMID: 2736244

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