Hematology and Oncology

Research Output 1963 2019

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11 Citations (Scopus)

Hb f-charlotte, an aγ variant with a threonine residue in position γ75 and a glycine residue in position γ136

Plaseska, D., Kutlar, F., Wilson, J. B., Fei, Y. J. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 6, p. 617-625 9 p.

Research output: Contribution to journalArticle

Threonine
Glycine
Blood
Substitution reactions
Genes
6 Citations (Scopus)

Hb f-cle or α2265(e9)lys → asn

Kutlar, A., Kutlar, F., Wilson, J. B., Webber, B. B., Gonzalez Redondo, J. M. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 185-188 4 p.

Research output: Contribution to journalArticle

Abnormal Hemoglobins
Fetal Hemoglobin
Peptide Mapping
Asparagine
Hispanic Americans
7 Citations (Scopus)

HB f-cobb OR α2aγ237(c3)TRP→GLY

Chen, S. S., Webber, B. B., Kutlar, A., Wilson, J. B. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 6, p. 617-619 3 p.

Research output: Contribution to journalArticle

Hemoglobins
Substitution reactions
Cells
hemoglobin A(0)
10 Citations (Scopus)

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

Hemoglobin M
Abnormal Hemoglobins
Fetal Hemoglobin
4 Citations (Scopus)

Hb f-jiangsu, the first γ chain variant with a valine -methionine substitution: Αgamma;2134(h12) val→met

Plaseska, D., Kutlar, F., Wilson, J. B., Webber, B. B., Zeng, Y. T. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 2, p. 177-183 7 p.

Research output: Contribution to journalArticle

methionylmethionine
Valine
Fetal Blood
Methionine
Substitution reactions

HB f-Kingston or α2 6γ255(d6)met→arg in a spanish newborn

Pablos, J. M. D., Wilson, J. B., Kutlar, A., Kutlar, F., Webber, B. B. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 5, p. 513-516 4 p.

Research output: Contribution to journalArticle

High pressure liquid chromatography
Abnormal Hemoglobins
Fetal Hemoglobin
Amino Acids
10 Citations (Scopus)

Hb f-oakd or α2gγi226(b8)glu → lys

Kleman, K., Lubin, B., Wilson, J. B., Kutlar, A., Webber, B. B. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 181-183 3 p.

Research output: Contribution to journalArticle

Abnormal Hemoglobins
Fetal Hemoglobin
DEAE-Cellulose Chromatography
Peptide Mapping
Glutamine
4 Citations (Scopus)

Hb f-onoda or α2gγ2146(HC3)histyr a newly discovered fetal hemoglobin variant in a japanese newborn

Harano, T., Harano, K., Doi, K., Ueda, S., Imai, K., Ohba, Y., Kutlar, F. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 2, p. 217-222 6 p.

Research output: Contribution to journalArticle

Fetal Hemoglobin
Gene Order
Globins
High performance liquid chromatography
Reverse-Phase Chromatography
4 Citations (Scopus)

Hb fort worth or α227 (b8)glu→glyβ2 in a black family from Canada

Carstairs, K. C., Raulfs, A., Kutlar, A., Chen, S. S., Webber, B. B., Wilson, J. B. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 2, p. 201-205 5 p.

Research output: Contribution to journalArticle

High pressure liquid chromatography
Abnormal Hemoglobins
Chromatography
Amino Acids
Hot Temperature

Hb fulton-georgia [α20(B1)His→Pro; HBA1: C.62A>C]: A new α-Globin variant coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC disease

Zhuang, L., Patel, N., Bryant, S., Kutlar, A., Kutlar, F. & Young, A. N., Sep 12 2013, In : Hemoglobin. 37, 5, p. 481-485 5 p.

Research output: Contribution to journalArticle

Hemoglobin SC Disease
Thalassemia
Globins
Hemoglobins
Genes
8 Citations (Scopus)

HB f-xin-su or aγt73(e17)asp→his: A new slow-moving fetal hemoglobin variant

Ma, M., Hu, H., Kutlar, F., Wilson, J. B. & Huismn, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 5, p. 473-479 7 p.

Research output: Contribution to journalArticle

Fetal Hemoglobin
Fetal Blood
Ethnic Groups
Blood
Substitution reactions
5 Citations (Scopus)

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

Blood Protein Electrophoresis
Abnormal Hemoglobins
Hemoglobin A
Fetal Hemoglobin
High Pressure Liquid Chromatography
1 Citation (Scopus)

Hb g-copenhagen or α2β 247(cd6)asp→asn observed in a black newborn

Chen, S. S., Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 4, p. 405-408 4 p.

Research output: Contribution to journalArticle

High pressure liquid chromatography
Abnormal Hemoglobins
Peptide Fragments
Asparagine
Aspartic Acid

Hb g-Taipei or β22(b4)glu → gly in a chinese family livinn the Netherlands

Landman, H., Wilson, J. B., Kutlar, A., Gonzalez Redondo, J. M. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 169-171 3 p.

Research output: Contribution to journalArticle

High pressure liquid chromatography
Abnormal Hemoglobins
Glutamine
Glycine
Amino Acids
9 Citations (Scopus)

Hb Hammersmith [β 42(CD1) Phe→Ser]: Occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies

McMorrow Tuohy, A. M., McKie, V. C., Sabio, H., Kutlar, F., Kutlar, A. & Wilson, J. B., Jan 1 1998, In : Journal of Pediatric Hematology/Oncology. 20, 6, p. 563-566 4 p.

Research output: Contribution to journalArticle

Monozygotic Twins
Mutation
African Americans
Hemolytic Anemia
Oximetry
13 Citations (Scopus)

Hb Hekinan observed in three chinese from macau; identification of the gag→gat mutation in the αl-globin gene

Zhao, W., Wilson, J. B., Webber, B. B., Kutlar, A., Tamagnini, G. P., Kuan, B. & Huisnan, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 6, p. 627-635 9 p.

Research output: Contribution to journalArticle

Macau
Globins
High performance liquid chromatography
Aspartic Acid
Purification
10 Citations (Scopus)

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

3 Citations (Scopus)

Hb inkster [α85(F6)asp→val] found in a caucasian male with polycythemia

Aguinaga, M. D. P., Kutlar, F., Turner, E. A. & Park, D., Jan 1 2000, In : Hemoglobin. 24, 4, p. 333-339 7 p.

Research output: Contribution to journalArticle

High pressure liquid chromatography
Abnormal Hemoglobins
Globins
hemoglobin Inkster
12 Citations (Scopus)

Hb J-Antakya or α2β265(E9)Lys → Met in a Turkish family and Hb Complutense or α2β2127(H5)Gln → Glu in a Spanish family; correction of a previously published identification

Huisman, T. H. J., Wilson, J. B., Kutlar, A., Yang, K. G., Chen, S. S., Webber, B. B., Altay, C. & Martinez, A. V., Jun 5 1986, In : Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular. 871, 2, p. 229-231 3 p.

Research output: Contribution to journalArticle

Substitution reactions
Communication
hemoglobin Complutense
hemoglobin J Antakya
6 Citations (Scopus)

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

Hemoglobin J
Abnormal Hemoglobins
5 Citations (Scopus)

Hb J- Meerut [α 120 (H3) Ala →Glu (α1)] in a Turkish male

Dinçol, G., Güvenç, S., Elam, D., Kutlar, A. & Kutlar, F., Feb 2 2006, In : International Journal of Medical Sciences. 3, 1, p. 26-27 2 p.

Research output: Contribution to journalArticle

Erythrocyte Count
Globins
Oxygen
Population
hemoglobin J Meerut
5 Citations (Scopus)

HB J-pontoise or α263(E12)ALA→ASPβ2 in four members of a Spanish family

Gonzalez Redondo, J. M., Wilson, J. B., Kutlar, A., Huisman, T. H., Sicilia, A., Romero, C. & Fernandes Fuertes, I., Aug 21 1987, In : Hemoglobin. 11, 1, p. 47-50 4 p.

Research output: Contribution to journalArticle

Hemoglobin J
Hemoglobins
Substitution reactions
Observation
11 Citations (Scopus)

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

High performance liquid chromatography
Electrophoresis
Spain
Hemoglobins
Substitution reactions
7 Citations (Scopus)

Hb lepore-Baltimore in a north sardinian family

Nasala, B., Manca, L., Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 3, p. 241-246 6 p.

Research output: Contribution to journalArticle

Abnormal Hemoglobins
Italy
Amino Acids
hemoglobin Lepore Baltimore
9 Citations (Scopus)

Hb M Dothan [β 25/26 (B7/B8)/(GGT/GAG→GAG//Gly/Glu→Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics

Kutlar, F., Hilliard, L. M., Zhuang, L., Patel, N., Eroglu, B., Meiler, S. E., Carmichael, H., Russell, R. B. & Kutlar, A., Nov 1 2009, In : Blood Cells, Molecules, and Diseases. 43, 3, p. 235-238 4 p.

Research output: Contribution to journalArticle

Methemoglobin
Globins
Hemoglobin M
Phenotype
Polymerase Chain Reaction
31 Citations (Scopus)

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

DNA Mutational Analysis
Abnormal Hemoglobins
RNA Splice Sites
Thalassemia
Gene Rearrangement
13 Citations (Scopus)

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

kyotorphin
Heme
Codon
Tyrosine
Oxygen
15 Citations (Scopus)

Hb oloc or α2β286(f2)ala → asp, a new high oxygen affinity variant

Indrak, K., Wiedermann, B. F., Batek, F., Wilson, J. B., Webber, B. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 2, p. 151-155 5 p.

Research output: Contribution to journalArticle

High pressure liquid chromatography
Abnormal Hemoglobins
Aspartic Acid
Alanine
Oxygen
7 Citations (Scopus)

HB p-nilotic or α2(βdelta;2 in a turkish family

Altay, C., Kutlar, A., Wilson, J. B., Webber, B. B. & Huisman, T. H. J., Jan 1 1987, In : Hemoglobin. 11, 4, p. 395-399 5 p.

Research output: Contribution to journalArticle

Sickle Hemoglobin
Siblings
Hemoglobins
Students
Hemoglobinopathies
14 Citations (Scopus)

Hb Q‐Thailand‐Hb H disease in a chinese living in Geneva, Switzerland: Characterization of the variant and identification of the two α‐thalassemic chromosomes

Beris, P., Huber, P., Miescher, P. A., Wilson, J. B., Kutlar, A., Chen, S. S. & Huisman, T. H. J., Jan 1 1987, In : American Journal of Hematology. 24, 4, p. 395-400 6 p.

Research output: Contribution to journalArticle

Globins
Switzerland
Chromosomes
Chromosome Mapping
Liquid Chromatography
23 Citations (Scopus)

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

Thalassemia
Mutation
Globins
Oligonucleotide Probes
Hematology
11 Citations (Scopus)

Hb saint louis or α2β228(b10)leu→gln in a czechoslovakian Male

Wiedermann, B. F., Indrak, K., Wilson, J. B., Webber, B. B., Yang, K. G., Kutlar, F., Kutlar, A. & Huisman, T. H. J., Jan 1 1986, In : Hemoglobin. 10, 6, p. 673-676 4 p.

Research output: Contribution to journalArticle

Hemoglobin M
Abnormal Hemoglobins
Czechoslovakia
Hematologic Tests
High Pressure Liquid Chromatography
6 Citations (Scopus)

Hb Setif [α94(G1)Asp→Tyr (α2)] Detected in a Turkish Family

Dinçol, G., Elam, D., Kutlar, A. & Kutlar, F., Dec 1 2003, In : Hemoglobin. 27, 4, p. 249-252 4 p.

Research output: Contribution to journalArticle

DNA Mutational Analysis
Abnormal Hemoglobins
Protein Denaturation
Family Health
Turkey
6 Citations (Scopus)

HB shelby [α2β2131(h9)GLN→LYS]-βdeg;thalassemia [codon 15 (TGG→TGA)] identified by DNA sequencing

Cürük, M. A., Kutlar, A. & Huisman, T. H. J., Jan 1 1992, In : Hemoglobin. 16, 5, p. 417-419 3 p.

Research output: Contribution to journalArticle

Abnormal Hemoglobins
DNA
26 Citations (Scopus)

Hb sun prae or α213o(h13)ala → proβ2 a new unstable variant occurring in low quantities

Harkness, M., Harkness, D. R., Kutlar, F., Kutlar, A., Wilson, J. B., Webber, B. B., Codrington, J. F. & Huisman, T. H. J., Jan 1 1990, In : Hemoglobin. 14, 5, p. 479-489 11 p.

Research output: Contribution to journalArticle

Solar System
Sun
Globins
Genes
Mutation
6 Citations (Scopus)

Hb zengcg or α2β2114(g16)leu → met

Plaseska, D., Wilson, J. B., Gu, L. H., Kutlar, F., Huisman, T. H. J., Zeng, Y. T. & Shen, M., Jan 1 1990, In : Hemoglobin. 14, 5, p. 555-557 3 p.

Research output: Contribution to journalArticle

Molecular Sequence Data
Abnormal Hemoglobins
Heterozygote
Amino Acid Sequence
Newborn Infant
32 Citations (Scopus)

Heat shock protein 90 inhibitors prevent lps-induced endothelial barrier dysfunction by disrupting Rhoa signaling

Joshi, A. D., Dimitropoulou, C., Thangjam, G., Snead, C., Feldman, S., Barabutis, N., Fulton, D., Hou, Y., Kumar, S., Patel, V., Gorshkov, B., Verin, A. D., Black, S. M. & Catravas, J. D., Jan 1 2014, In : American journal of respiratory cell and molecular biology. 50, 1, p. 170-179 10 p.

Research output: Contribution to journalArticle

HSP90 Heat-Shock Proteins
tanespimycin
Endothelial cells
Myosin Light Chains
Phosphorylation
10 Citations (Scopus)

Helicobacter pylori Infection in Sickle Cell Disease

Woods, K. F., Onuoha, A., Schade, R. R. & Kutlar, A., Jul 1 2000, In : Journal of the National Medical Association. 92, 7, p. 361-365 5 p.

Research output: Contribution to journalArticle

Sickle Cell Anemia
Helicobacter Infections
Helicobacter pylori
Peptic Ulcer
Abdominal Pain
37 Citations (Scopus)

Hematological observations on arabian SS patients with a homozygosity or heterozygosity for a βs chromosome with haplotype 31

Kutlar, A., Hattori, Y., Bakioglu, I., Kutlar, F., Huisman, T. H. J. & Kamel, K., Jan 1 1985, In : Hemoglobin. 9, 6, p. 545-557 13 p.

Research output: Contribution to journalArticle

Chromosomes
Haplotypes
Sickle Cell Anemia
Heterozygote
Hemoglobins
45 Citations (Scopus)

HemoglobinBibba or α2136Pro β2, an unstable α chain abnormal hemoglobin

Kleihauer, E. F., Reynolds, C. A., Dozy, A. M., Wilson, J. B., Moores, R. R., Berenson, M. P., Wright, C. S. & Huisman, T. H. J., Jan 22 1968, In : BBA - Protein Structure. 154, 1, p. 220-222 3 p.

Research output: Contribution to journalArticle

Autoanalysis
Congenital Hemolytic Anemia
Abnormal Hemoglobins
Ion Exchange Chromatography
Splenectomy
17 Citations (Scopus)

Hemoglobin binding to Aβ and HBG2 SNP association suggest a role in Alzheimer's disease

Perry, R. T., Gearhart, D. A., Wiener, H. W., Harrell, L. E., Barton, J. C., Kutlar, A., Kutlar, F., Ozcan, O., Go, R. C. P. & Hill, W. D., Feb 1 2008, In : Neurobiology of Aging. 29, 2, p. 185-193 9 p.

Research output: Contribution to journalArticle

gamma-Globins
Fetal Hemoglobin
Poisons
Heme
Single Nucleotide Polymorphism
9 Citations (Scopus)

Hemoglobin Birmingham and hemoglobin Galicia: Two unstable β chain variants characterized by small deletions and insertions

Wilson, J. B., Webber, B. B., Hu, H., Kutlar, A., Kutlar, F., Codrington, J. F., Prchal, J. T., Hall, K. M., De Pablos, J. M., Rodriguez, I. & Huisman, T. H. J., Jan 1 1990, In : Blood. 75, 9, p. 1883-1887 5 p.

Research output: Contribution to journalArticle

DNA-Directed DNA Polymerase
Glutamine
Codon
Leucine
Hemoglobins
2 Citations (Scopus)

Hemoglobin daneshgah-Tehran or α272(ef1)his→argβ2 in an argentinean family

De Weinstein, B. I., Kutlar, A., Webber, B. B., Wilson, J. B. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 4, p. 409-411 3 p.

Research output: Contribution to journalArticle

High pressure liquid chromatography
Abnormal Hemoglobins
Macromolecular Substances
Peptide Fragments
Argentina
2 Citations (Scopus)

Hemoglobin F only syndrome at birth: A case of maternal HbA2' complicating the diagnosis of β-thalassemia

Yee, M. E. M., Quarmyne, M. O., Segbefia, C., Young, A. N., Zhuang, L. & Kutlar, F., Jan 1 2016, In : Journal of Pediatric Hematology/Oncology. 38, 1, p. e32-e34

Research output: Contribution to journalArticle

Fetal Hemoglobin
Thalassemia
Globins
Mothers
Parturition
2 Citations (Scopus)

Hemoglobin h disease in two turkish females and one iranian newborn

Aksoy, M., Kutlar, A., Kutlar, F., Harano, T., Chen, S. S. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 4, p. 373-384 12 p.

Research output: Contribution to journalArticle

Globins
Hemoglobins
Genes
Chromosomes
Thalassemia
4 Citations (Scopus)

Hemoglobin o-padova or α230(b11)GLU→LYSβ2 observed in members of a turkish family

Kilinç, Y., Kumi, M., Gurgey, A., Altay, C., Webber, B. B., Wilson, J. B., Kutlar, A. & Huisman, T. H. J., Jan 1 1985, In : Hemoglobin. 9, 6, p. 621-625 5 p.

Research output: Contribution to journalArticle

Hemoglobins
Hemoglobin C
Fathers
Siblings
Blood
41 Citations (Scopus)

Hemoglobinopathies among the gond tribal groups of central India; interaction of α and βthalassemia with β chain variants

Gupta, R. B., Tiwary, R. S., Pande, P. L., Kutlar, F., Öner, C., Öner, R. & Huisman, T. H. J., Jan 1 1991, In : Hemoglobin. 15, 5, p. 441-458 18 p.

Research output: Contribution to journalArticle

Abnormal Hemoglobins
Globins
12 Citations (Scopus)

Hepatic failure caused by plasma cell infiltration in multiple myeloma

Rahhal, F. E., Schade, R. R., Nayak, A. & Coleman, T. A., Apr 28 2009, In : World Journal of Gastroenterology. 15, 16, p. 2038-2040 3 p.

Research output: Contribution to journalArticle

Liver Failure
Plasma Cells
Multiple Myeloma
Liver Diseases
Thalidomide
48 Citations (Scopus)

Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the Gγ and Aγ types of γ chain

Kutlar, A., Gardiner, M. B., Headlee, M. G., Reese, A. L., Cleek, M. P., Nagle, S., Sukumaran, P. K. & Huisman, T. H. J., Feb 1 1984, In : Biochemical Genetics. 22, 1-2, p. 21-35 15 p.

Research output: Contribution to journalArticle

Fetal Hemoglobin
DNA Restriction Enzymes
hemoglobin
Heterozygote
heterozygosity
1 Citation (Scopus)

Heterogeneity of γ-globin chain synthesis in Saudi newborns

Niazi, G. A., Yaish, H. M., Kutlar, F. & Huisman, T. H. J., Jan 1 1991, In : International Journal of Hematology. 54, 5, p. 377-383 7 p.

Research output: Contribution to journalArticle

Globins
Fetal Hemoglobin
Gene Order
Saudi Arabia
Multigene Family