Hematology and Oncology

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1989

HB extremadura or α2β2133(h11)VAU→LEU, a new mildly unstable hemoglobin in a Spanish female

Villegas, A., Martín, G., Wilson, J. B., Webber, B. B., Hu, H., Kutlar, A., Kutlar, F. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 5, p. 505-508 4 p.

Research output: Contribution to journalArticle

12 Scopus citations

HB f-h-Osaka or (α2gγ;263(e7)HIS→TYR in a caucasian male infant

Glader, B. E., Zwerdling, D., Kutlar, F., Kutlar, A., Wilson, J. B. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 7-8, p. 769-773 5 p.

Research output: Contribution to journalArticle

10 Scopus citations

Hb gainesville-ga or α2β246(cd5) gly→arg; second report

Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 6, p. 623-624 2 p.

Research output: Contribution to journalArticle

6 Scopus citations

Hb Himeji or α2β2140(h18)ala→asp in a portuguese family

Martins, M. C., Rosado, L., Wilson, J. B., Kutlar, A., Hu, H. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 4, p. 411-415 5 p.

Research output: Contribution to journalArticle

10 Scopus citations

HB j-Lome or α2β259(e3)LYS→ASN in a vietnamese family

Prior, J. F., Raven, J. L., Wilson, J. B., Kutlar, A., Kutlar, F. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 1, p. 79-81 3 p.

Research output: Contribution to journalArticle

6 Scopus citations

HB monroe or α2β230(b12)ARG→THR, a variant associated with βthalassemia due to a g→c substitution adjacent to the donor splice site of the first intron

Gonzalez-Redondo, J. M., Stoming, T. A., Kutlar, F., Kutlar, A., Hu, H., Wilson, J. B. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 1, p. 67-74 8 p.

Research output: Contribution to journalArticle

31 Scopus citations

Hydrops fetalis due to homozygosity for α-thalassemia-1, -(α)-20.5 kb: The first observation in a Turkish family

Gurgey, A., Altay, Beksaç, M. S., Bhattacharya, R., Kutlar, F. & Huisman, T. H. J., Jan 1 1989, In : Acta Haematologica. 81, 3, p. 169-171 3 p.

Research output: Contribution to journalArticle

14 Scopus citations

Mechanisms for the stimulation of prostanoid synthesis by cyclosporine and bacterial lipopolysacch aride

Zhang, H., Kaseki, H., Davis, W. B., Whisler, R. L. & Cornwell, D. G., Jan 1 1989, In : Transplantation. 47, 5, p. 864-871 8 p.

Research output: Contribution to journalArticle

7 Scopus citations

Molecular characterization of β‐globin gene mutations in Malay patients with Hb E‐β‐thalassaemia and thalassaemia major

Yang, K. G., Kutlar, F., George, E., Wilson, J. B., Kutlar, A., Stoming, T. A., Redondo, J. M. G. & Huisman, T. H. J., May 1989, In : British Journal of Haematology. 72, 1, p. 73-80 8 p.

Research output: Contribution to journalArticle

84 Scopus citations

Molecular heterogeneity of beta-thalassemia intermedia in turkey

Gurgey, A., Altay, Diaz-Chico, J. C., Kutlar, F., Kutlar, A. & Huisman, T. H. J., Jan 1 1989, In : Acta Haematologica. 81, 1, p. 22-27 6 p.

Research output: Contribution to journalArticle

20 Scopus citations

Normal Fetal Hemoglobin Levels in the Sudden Infant Death Syndrome

Zielke, H. R., Meny, R. G., O'brien, M. J., Smialek, J. E., Kutlar, F., Huisman, T. H. J. & Dover, G. J., Nov 16 1989, In : New England Journal of Medicine. 321, 20, p. 1359-1364 6 p.

Research output: Contribution to journalArticle

19 Scopus citations

Phenotype and function of T lymphocytes infiltrating the skin during graft-versus-host disease following allogeneic bone marrow transplantation

Kasten-Sportès, C., Masset, M., Varrin, F., Devergie, A. & Gluckman, E., Apr 1989, In : Transplantation. 47, 4, p. 621-624 4 p.

Research output: Contribution to journalArticle

19 Scopus citations

Quantitation of hemoglobins Bart's, H, Portland-I, Portland-II and constant spring by anion-exchange high-performance liquid chromatography

Kutlar, F., Gu, L. H., Hu, H. & Huisman, T. H. J., 1989, In : Journal of Chromatography B: Biomedical Sciences and Applications. 487, C, p. 265-274 10 p.

Research output: Contribution to journalArticle

12 Scopus citations

Severe Hb S-β°-thalassaemia with a T→C substitution in the donor splice site of the first intron of the β-globin gene

Gonzalez-Redondo, J. M., Stoming, T. A., Kutlar, F., Kutlar, A., McKie, V. C., McKie, K. M. & Huisman, T. H. J., Jan 1 1989, In : British Journal of Haematology. 71, 1, p. 113-117 5 p.

Research output: Contribution to journalArticle

41 Scopus citations

Studies on oxidized low density lipoproteins. Controlled oxidation and a prostaglandin artifact

Zhang, H., Davis, W. B., Chen, X., Whisler, R. L. & Cornwell, D. G., Jan 1 1989, In : Journal of Lipid Research. 30, 2, p. 141-148 8 p.

Research output: Contribution to journalArticle

17 Scopus citations

The levels of ζ, γ, and δ chains in patients with Hb H disease

Kutlar, F., Gonzalez-Redondo, J. M., Kutlar, A., Gurgey, A., Altay, Ç., Efremov, G. D., Kleman, K. & Huisman, T. H. J., May 1 1989, In : Human Genetics. 82, 2, p. 179-186 8 p.

Research output: Contribution to journalArticle

32 Scopus citations

The types of hemoglobins and globin chains in hydrops fetalis

Kutlar, F., Reese, A. L., Hsia, Y. E., Kleman, K. M. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 7-8, p. 671-683 13 p.

Research output: Contribution to journalArticle

14 Scopus citations

Two rare unstable β chain variants, HB mozhaisk or α2β292(f8)his ARG and HB DJELFA or α2β298(FG5)VAL→ALA, each being observed for the second time

Bird, A. R., Elliott, T., Wison, J. B., Webber, B. B., Hu, H., Kutlar, A., Kutlar, F. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 2, p. 193-197 5 p.

Research output: Contribution to journalArticle

6 Scopus citations

α‐thalassemia among Pediatric Hemoglobin S Homozygotes: Molecular and Clinical Studies

FELICE, A. E., ZHAO, J., KUTLAR, A., RHODES, M., McKie, K. & McKie, V., Jul 1989, In : Annals of the New York Academy of Sciences. 565, 1, p. 381-382 2 p.

Research output: Contribution to journalArticle

βthalassemia intermedia in two turkish families is caused by the interaction of HB knossos [β27(b9)ALA→SER] and of HB city of Hope [β69(e13)gly→ser] with b°thalassemia

Kutlar, A., Kutlar, F., Aksoy, M., Gurgey, A., Altay, C., Wilson, J. B., Diaz-Chico, J. C., Hu, H. & Huisman, T. H. J., Jan 1 1989, In : Hemoglobin. 13, 1, p. 7-16 10 p.

Research output: Contribution to journalArticle

18 Scopus citations
1988

A chromosome with five γ-globin genes

Fei, Y. J., Lanclos Ke., D., Kutlar, F., Walker, E. F. & Huisman, T. H. J., Jan 1 1988, In : Blood. 72, 2, p. 827-829 3 p.

Research output: Contribution to journalArticle

7 Scopus citations

Biochemical and molecular aspects of βthalassemia types in northern sardinia

Masala, B., Manca, L., Gallisai, D., Stangoni, A., Lanclos, K. D., Kutlar, F., Yang, K. G. & Huisnan, T. H. J., Jan 1 1988, In : Hemoglobin. 12, 5-6, p. 661-671 11 p.

Research output: Contribution to journalArticle

13 Scopus citations

Characterization of abnormalities in the γglobin gene arrangements of japanese newborns

Harano, T., Harano, K., Ukita, H., Wada, Y., Hayashi, A., Ohba, Y., Miyaji, T., Kutlar, F. & Huisman, T. H. J., Jan 1 1988, In : Hemoglobin. 12, 5-6, p. 723-739 17 p.

Research output: Contribution to journalArticle

8 Scopus citations

Clinical and genetic heterogeneity in black patients with homozygous β-thalassemia from the Southeastern United States

Gonzalez-Redondo, J. M., Stoming, T. A., Lanclos, K. D., Gu, Y. C., Kutlar, A., Nakatsuji, T., Deng, B., Han, I. S., McKie, V. C. & Huisman, T. H. J., Jan 1 1988, In : Blood. 72, 3, p. 1007-1014 8 p.

Research output: Contribution to journalArticle

145 Scopus citations

HB duan [α75(EF4)ASP→ALA), HB Westmead [α122(h5)HIS→GLN], and αthalassemia-2 (-4.2 KB deletion) in a chinese family

Liang, S., Tang, Z., Su, C., Lung, Q., Liang, R., Fei, Y. J., Kutlar, F., Wilson, J. B., Mebber, B. B., Hu, H. & Huisman, T. H. J., Jan 1 1988, In : Hemoglobin. 12, 1, p. 13-21 9 p.

Research output: Contribution to journalArticle

9 Scopus citations

Hb las palms or α2β249(cd8)ser→phe, a mildly unstable hemiglobin variant

Malcorra-Azpiazu, J. J., Balda-Aguirre, H. I., Diaz-Chico, J. C., Hu, H., Wilson, J. B., Webber, B. B., Kutlar, F., Kutlar, A. & Huisman, T. H. J., Jan 1 1988, In : Hemoglobin. 12, 2, p. 163-170 8 p.

Research output: Contribution to journalArticle

11 Scopus citations

Hb Natal or α2(minus Tyr-Arg)β2: A high oxygen affinity α chain variant with a deleted carboxy-terminus resulting from a TAC → TAA (Tyr → terminating codon) mutation in codon α140

Jogessar, V. B., Westermeyer, K., Webber, B. B., Wilson, J. B., Hu, H., Gonzalez-Redondo, J. M., Kutlar, A. & Huisman, T. H. J., Nov 10 1988, In : BBA - Gene Structure and Expression. 951, 1, p. 36-41 6 p.

Research output: Contribution to journalArticle

13 Scopus citations

Hb S(c)-β+ -thalassaemia: Different mutations are associated with different levels of normal Hb A

Gonzalez-Redondo, J. M., Kutlar, F., Kutlar, A., Stoming, T. A., De Pablos, J. M., Kilinc, Y. & Huisman, T. H. J., Jan 1 1988, In : British Journal of Haematology. 70, 1, p. 85-89 5 p.

Research output: Contribution to journalArticle

23 Scopus citations

Inclusion body β-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended β chain carboxy-terminus due to a modification in codon β114

Beris, P., Miescher, P. A., Diaz-Chico, J. C., Han, I. S., Kutlar, A., Hu, H., Wilson, J. B. & Huisman, T. H. J., Jan 1 1988, In : Blood. 72, 2, p. 801-805 5 p.

Research output: Contribution to journalArticle

51 Scopus citations

Mild and severe β-thalassemia among homozygotes from Turkey: Identification of the types by hybridization of amplified DNA with synthetic probes

Diaz-Chico, J. C., Yang, K. G., Stoming, T. A., Efremov, D. G., Kutlar, A., Kutlar, F., Aksoy, M., Altay, C., Gurgey, A., Kilinc, Y. & Huisman, T. H. J., Jan 1 1988, In : Blood. 71, 1, p. 248-251 4 p.

Research output: Contribution to journalArticle

83 Scopus citations

Quantification of hemoglobins S, C, and F by a magnetic affinity immunoassay

Moscoso, H., Kiefer, C. R., Kutlar, A. & Garver, F. A., Jan 1 1988, In : Clinical Chemistry. 34, 5, p. 902-905 4 p.

Research output: Contribution to journalArticle

10 Scopus citations

Some rare hemoglobin variants with altered oxygen affinities; hb linkoping [β36(c2)pro→thr], hb caribbean [β91(f7)leu→ar6], and hb sunnybrook [β 36(c2)pro→arg]

Ali, M. A. M., Pinkerton, P., Chow, S. W. S., Zaetz, S. D., Wilson, J. B., Webber, B. B., Hu, H., Kutlar, F. & Huisman, T. H. J., Jan 1 1988, In : Hemoglobin. 12, 2, p. 137-148 12 p.

Research output: Contribution to journalArticle

16 Scopus citations
21 Scopus citations
20 Scopus citations

Upstream promoter mutation associated with a modest elevation of fetal hemoglobin expression in human adults

Gilman, J. G., Mishima, N., Wen, X. J., Kutlar, F. & Huisman, T. H. J., Jan 1 1988, In : Blood. 72, 1, p. 78-81 4 p.

Research output: Contribution to journalArticle

28 Scopus citations

Variation in clinical severity among patients with Hb Lepore-Boston-β-thalassaemia is related to the type of β-thalassaemia

Efremov, D. G., Efremov, G. D., Zisovski, N., Stojanovski, N., Kutlar, F., Diaz-Chico, J. C., Kutlar, A., Yang, K. G., Stoming, T. A. & Huisman, T. H. J., Jan 1 1988, In : British Journal of Haematology. 68, 3, p. 351-355 5 p.

Research output: Contribution to journalArticle

27 Scopus citations

Variations in gγ, and aγ ratios in the fetal hemiglobin of newborn babies

Huisman, T. H. J., Fei, Y. J. & Kutlar, F., Jan 1 1988, In : Hemoglobin. 12, 5-6, p. 699-705 7 p.

Research output: Contribution to journalArticle

7 Scopus citations
1987

Adult hemoglobin levels in newborn babies from different countries and in babies with some significant hemoglobinopathies

Kutlar, F., Kutlar, A., Gu, Y. C. & Huisman, T. H. J., Jan 1 1987, In : Acta Haematologica. 78, 1, p. 28-32 5 p.

Research output: Contribution to journalArticle

10 Scopus citations

A G to A nucleotide substitution 161 base pairs 5' of the G gamma globin gene cap site (-161) in a high G gamma non-anemic person.

Gilman, J. G., Kutlar, F., Johnson, M. E. & Huisman, T. H., Jan 1 1987, In : Progress in Clinical and Biological Research. 251, p. 383-390 8 p.

Research output: Contribution to journalArticle

12 Scopus citations

An ~300 bp deletion involving part of the 5' β-globin gene region is observed in members of a Turkish family with β-thalassemia

Diaz-Chico, J. C., Yang, K. G., Kutlar, A., Reese, A. L., Aksoy, M. & Huisman, T. H. J., Jan 1 1987, In : Blood. 70, 2, p. 583-586 4 p.

Research output: Contribution to journalArticle

30 Scopus citations

An indonesian family with the southeast asian type of α-thalassemia-1 and a γ-globin gene triplication

Daenen, S., Reese, A. L., Kutlar, F. & Huisman, T., Jan 1 1987, In : Acta Haematologica. 78, 1, p. 23-27 5 p.

Research output: Contribution to journalArticle

1 Scopus citations

Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya

Lanclos, K. D., Patterson, J., Efremov, G. D., Wong, S. C., Villegas, A., Ojwang, P. J., Wilson, J. B., Kutlar, F. & Huisman, T. H. J., Jan 1 1987, In : Human Genetics. 77, 1, p. 40-45 6 p.

Research output: Contribution to journalArticle

21 Scopus citations

Detection of the embryonic ζ chain in blood from newborn babies by reversed-phase high-perfomance liquid chromatogrphy

Kutlar, F., Fei, Y. J., Wilson, J. B., Kutlar, A. & Huisman, T. H. J., 1987, In : Journal of Chromatography A. 394, 2, p. 333-343 11 p.

Research output: Contribution to journalArticle

18 Scopus citations

Effects of α‐thalassemia‐2 on the developmental changes of hematological values in children with sickle cell disease from georgia

Felice, A. E., McKie, K. M., Cleek, M. P., Marino, E. M., Kutlar, A. & McKie, V. C., Jan 1 1987, In : American Journal of Hematology. 25, 4, p. 389-400 12 p.

Research output: Contribution to journalArticle

18 Scopus citations

Fetal hemoglobin heterogeneity in chinese newborns of the uygur and han nationalities; comparisons of babies from xinjiang and Beijing

Chu, Z. F., Liang, C. C., Kutalar, F. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 123-128 6 p.

Research output: Contribution to journalArticle

4 Scopus citations

Haplotypes and α globin gene analyses in sickle cell anaemia patients from Kenya

Ojwang, P. J., Ogada, T., Beris, P., Hattori, Y., Lanclos, K. D., Kutlar, A., Kutlar, F. & Huisman, T. H. J., Jan 1 1987, In : British Journal of Haematology. 65, 2, p. 211-215 5 p.

Research output: Contribution to journalArticle

42 Scopus citations

Hb borås or α2β288(f4)leu → arg in a south african female

Bird, A. R., Elliot, T. E., Wilson, J. B., Webber, B. B., Kutlar, F., Kutlar, A. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 157-160 4 p.

Research output: Contribution to journalArticle

1 Scopus citations

Hb bushwick [β74(e18)GLY→VAL] heterozygotes in a yugoslavian family have 35 to 40% of the unstable variant

Efremov, G. D., Jankovic, L., Juricic, D., Stojancov, A., Wilson, J. B., Webber, B. B., Kutlar, F., Kutlar, A., Hu, H. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 6, p. 557-562 6 p.

Research output: Contribution to journalArticle

3 Scopus citations

Hb d-Granada or α2β222(b4)GLU→VAL

De Pablos, J. M., Kutlar, A., Wilson, J. B., Webber, B. B., Hu, H. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 6, p. 563-565 3 p.

Research output: Contribution to journalArticle

6 Scopus citations

Hb e-Saskatoon or α2β222(b4)glu→lys in a spanish family

Gonzalez Redondo, J. M., Sicilia, A., Murga, M. J., Kutlar, A., Wilson, J. B. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 1, p. 35-38 4 p.

Research output: Contribution to journalArticle

5 Scopus citations