E. Baysal

发表

Modulation of iron-mediated oxidant damage in erythrocytes by cellular energy levels.

C. Rice-Evans, E. Baysal, C. Rice-evans, 1987, Free radical research communications.

t-butyl hydroperoxide-induced perturbations of human erythrocytes as a model for oxidant stress.

C. Rice-Evans, P. Hochstein, D. Pashby, 1985, Biochimica et biophysica acta.

Polymorphic pattern of the (AT)x(T)y motif at −530 5′ to the β‐globin gene in over 40 patients homozygous for various β‐thalassemia mutations

V. Divoky, T. Huisman, A. Adekile, 1994 .

Polymorphic pattern of the (AT)X(T)Y motif at -530 5' to the beta-globin gene in over 40 patients homozygous for various beta-thalassemia mutations.

V. Divoky, T. Huisman, A. Adekile, 1994, American journal of hematology.

ICSH recommendations for the measurement of Haemoglobin F

J. Hoyer, S. Fucharoen, A. Mosca, 2012, International journal of laboratory hematology.

Desferrioxamine protects human red blood cells from hemin-induced hemolysis.

A. Stern, E. Baysal, S. G. Sullivan, 1990, Free radical biology & medicine.

Iron-mediated oxidative stress in erythrocytes.

C. Rice-Evans, E. Baysal, Erol Baysal, 1987, The Biochemical journal.

β‐thalassemia alleles and unstable hemoglobin types among russian pediatric patients

T. Huisman, N. S. Smetanina, Y. Postnikov, 1994, American journal of hematology.

Molecular characterization of β-thalassemia in Czechoslovakia

M. Jarošová, K. Indrák, Y. Fei, 1992, Human Genetics.

Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions

C. Farra, V. Viprakasit, H. Najmabadi, 2007, Clinical chemistry and laboratory medicine.

Beta-thalassemia mutations in the Portuguese; high frequencies of two alleles in restricted populations.

T. Huisman, M. Ribeiro, J. Kaeda, 1993, Hemoglobin.

An IVS‐I‐117 (G→A) acceptor splice site mutation in the α 1‐globin gene is a nondeletional α‐thalassaemia‐2 determinant in an Indian population

E. Baysal, T. Huisman, S. Sharma, 1993 .

A large beta-thalassemia deletion in a family of Indonesian-Malay descent.

T. Huisman, A. Dimovski, D. Efremov, 1996, Hemoglobin.

Sickle cell anemia, sickle cell β-thalassemia, and thalassemia major in Albania: characterization of mutations

V. Divoky, A. Adekile, A. Dimovski, 1994, Human Genetics.

Molecular characterization of β-thalassemia in Azerbaijan

G. Yüreğir, M. Ribeiro, E. Baysal, 1992, Human Genetics.

Compound heterozygosity for a β∘-thalassemia (frameshift codons 38/39; -C) and a nondeletional swiss type of HPFH (A→C at NT -110, Gγ) in a Czechoslovakian family

D. Pospíšilová, K. Indrák, T. Huisman, 1991, Annals of Hematology.

Inhibition of hemin-induced hemolysis by desferrioxamine: binding of hemin to red cell membranes and the effects of alteration of membrane sulfhydryl groups.

A. Stern, E. Baysal, S. G. Sullivan, 1992, Biochimica et biophysica acta.

A de novo Deletion Causing εγδβ-Thalassemia in a Dutch Patient

L. Bernini, T. Huisman, N. S. Smetanina, 1996 .

Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β‐thalassaemia due to a homozygosity for the IVS‐I‐6 (T→C) mutation

T. Huisman, A. Gürgey, G. Schilirò, 1994, British journal of haematology.

The β- and δ-Thalassemia Repository (Eighth Edition)

E. Baysal, M. F. Carver, 1995 .

A Czechoslovakian teenager with Hb E-β∘-thalassemia [IVS-I-1 (G → A)] complicated by the presence of an α-globin gene triplication

K. Indrák, Y. Fei, T. Huisman, 1991, Annals of Hematology.

The T→C mutation at position +96 of the untranslated region 3′ to the terminating codon of the β-globin gene is a rare polymorphism that does not cause a β-thalassemia as previously ascribed

V. Divoky, K. Indrák, E. Baysal, 2004, Human Genetics.

Sickle cell membranes and oxidative damage.

C. Rice-Evans, E. Baysal, S. Omorphos, 1986, The Biochemical journal.

ICSH recommendations for the measurement of Haemoglobin A2

J. Hoyer, S. Fucharoen, A. Mosca, 2012, International journal of laboratory hematology.

The β‐thalassaemia mutations in the population of Cyprus

K. Indrák, P. Ioannou, M. Angastiniotis, 1992 .

HB Coimbra or α2β299(Gl)ASP→GLU, A Newly Discovered High Oxygen Affinity Variant

T. Huisman, M. Ribeiro, E. Baysal, 1991 .

Oxidative effects of iron on erythrocytes.

C. Rice-Evans, A. Hoffbrand, G. Kontoghiorghes, 1985, Free radical research communications.

Genotype-phenotype correlation of sickle cell disease in the United Arab Emirates.

E. Baysal, S. El-kalla, Erol Baysal, 1998, Pediatric hematology and oncology.

GENOTYPE-PHENOTYPE CORRELATION OF SICKLE CELL DISEASE IN

U. Emirates, Arab Emirates, E. Baysal, 1998 .

Prooxidant and antioxidant effects of ascorbate on tBuOOH-induced erythrocyte membrane damage.

A. Stern, E. Baysal, S. G. Sullivan, 1989, The International journal of biochemistry.

Detection of common deletional α‐thalassemia‐2 determinants by PCR

E. Baysal, T. Huisman, 1994 .

Thalassemia intermedia in two patients with Hb lepore-β°-thalassemia (Frameshift codon 8, -AA)

T. Huisman, E. Baysal, L. Gu, 1994 .

Black β‐thalassemia homozygotes with specific sequence variations in the 5′ hypersensitive site‐2 of the locus control region have high levels of fetal hemoglobin

T. Huisman, A. Dimovski, P. Beris, 1992, American journal of hematology.

Molecular Characterization of α-Thalassemia Determinants, β-Thalassemia Alleles, and βs Haplotypes among Kuwaiti Arabs

T. Huisman, A. Adekile, M. Haider, 1994 .

Distribution of beta-thalassemia mutations in three Asian Indian populations with distant geographical locations.

T. Huisman, S. Wong, E. Baysal, 1994, Hemoglobin.

Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.

Y. Fei, T. Huisman, A. Gurgey, 1992, Acta haematologica.

Hb H disease in a Turkish family resulting from the interaction of a deletional α‐thalassaemia‐1 and a newly discovered poly A mutation

Y. Fei, T. Huisman, N. Dikmen, 1992, British journal of haematology.

Types of thalassemia among patients attending a large university clinic in Kuala Lumpur, Malaysia.

Y. Fei, J. Nechtman, E. Baysal, 1992, Hemoglobin.

Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1‐globin variant, observed in combination with the ‐(α)20.5 KB α‐thal‐1 deletion in two Turkish patients

T. Huisman, A. Gürgey, A. Gurgey, 1993 .

Molecular characterization of Hb S(C) β‐thalassemia in American blacks

A. Kutlar, T. Huisman, V. Mckie, 1991 .

HB Mizuho or α2β268(E12)Leu→pro in a Caucasian Boy with high levels of HB F; Identification by Sequencing of Amplified DNA

S. Bertolone, T. Huisman, E. Baysal, 1991 .

Hb Costa Rica or α2β277(EF1)His→Arg: The first example of a somatic cell mutation in a globin gene

N. S. Smetanina, M. Castillo, E. Baysal, 1996, Human Genetics.

Hb Costa Rica or ·2‚277(EF1)His→Arg: the first example of a somatic cell mutation in a globin gene

T. Huisman, N. S. Smetanina, M. Castillo, 1996, Human Genetics.

Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.

D. Pospíšilová, K. Indrák, T. Huisman, 1991, Annals of hematology.

Role of membrane-bound haemoglobin products in oxidative damage in sickle cell membranes.

C. Rice-Evans, E. Baysal, 1987, Acta haematologica.

Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs.

T. Huisman, A. Adekile, M. Haider, 1994, Acta haematologica.

Molecular Basis of β-Thalassemia in the United Arab Emirates

E. Baysal, 2011, Hemoglobin.

α-Thalassemia Syndromes in the United Arab Emirates

E. Baysal, 2011, Hemoglobin.

PRESENTED AT THE INTERNATIONAL CONFERENCE ON HEMOGLOBIN DISORDERS, KUWAIT, February 5-7th, 2011 MOLECULAR BASIS OF β-THALASSEMIA IN THE UNITED ARAB EMIRATES

U. Emirates, E. Baysal, 2011 .

The relative levels of α2-, α1-, and ζ-mRNA in HB H patients with different deletional and nondeletional α-thalassemia determinants

T. Huisman, N. S. Smetanina, A. Adekile, 1996 .

Alpha-Thalassemia and fetal hemoglobin [letter]

T. Huisman, E. Baysal, W. Qin, 1994 .

A novel deletion of approximately 27 kb including the beta-globin gene and the locus control region 3'HS-1 regulatory sequence: beta zero-thalassemia or hereditary persistence of fetal hemoglobin?

T. Huisman, A. Adekile, A. Dimovski, 1994, Blood.

A mild type of Hb S‐β+‐thalassemia [‐92(C→T)] in a sicilian family

E. Baysal, T. Huisman, V. Divoký, 1993 .

A mild type of Hb S-beta(+)-thalassemia [-92(C-->T)] in a Sicilian family.

T. Huisman, G. Schilirò, E. Baysal, 1993, American journal of hematology.

α‐Thalassaemia in the population of Cyprus

M. Angastiniotis, M. Kleanthous, P. Ioannou, 1995 .

A Repository of Deletional HPFH and δβ-Thalassemia Conditions

E. Baysal, 1993 .

HEMOGLOBINOPATHIES IN THE UNITED ARAB EMIRATES

E. Baysal, 2001, Hemoglobin.

α-Thalassemia in the United Arab Emirates

E. Baysal, S. El-kalla, 1998, Acta Haematologica.

The molecular basis of Hb H disease in Turkey.

A. Gürgey, E. Baysal, Ç. Altay, 1997, Hemoglobin.

Rare β‐thalassemia mutation IVS‐II‐848 (C‐A) first reported in a Turkish cypriot family

A. Başak, E. Baysal, Sürkü Tüzmen, 1997, American journal of hematology.

Molecular Heterogeneity of Beta-Thalassemia in the United Arab Emirates

E. Baysal, 2005, Public Health Genomics.

alpha-thalassemia in the United Arab Emirates.

E. Baysal, S. El-kalla, 1998, Acta haematologica.

The beta-thalassaemia mutations in the population of Cyprus.

K. Indrák, P. Ioannou, M. Angastiniotis, 1992, British journal of haematology.

Validation of a semiconductor next-generation sequencing assay for the clinical genetic screening of CFTR

Maximilian E. R. Weiss, K. Kandaswamy, C. Farra, 2015, Molecular genetics & genomic medicine.

The relative levels of alpha 2-, alpha 1-, and zeta-mRNA in HB H patients with different deletional and nondeletional alpha-thalassemia determinants.

T. Huisman, A. Gürgey, N. S. Smetanina, 1996, Biochimica et biophysica acta.

The Unstable HB Hammersmith or α2β242(CD1)PHE→SER Observed in an Indian Child; Identification by HPLC AND by Sequence Analysis of Amplified DNA

T. Huisman, N. Kobrinsky, E. Baysal, 1992 .

Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.

T. Huisman, A. Gürgey, A. Dimovski, 1993, American journal of hematology.

A Czechoslovakian teenager with Hb E-beta zero-thalassemia [IVS-I-1 (G----A)] complicated by the presence of an alpha-globin gene triplication.

K. Indrák, Y. Fei, T. Huisman, 1991, Annals of hematology.

Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.

S. Zeinali, M. Naderi, R. Mahdian, 2009, Blood cells, molecules & diseases.

Detection of common deletional alpha-thalassemia-2 determinants by PCR.

T. Huisman, E. Baysal, 1994, American journal of hematology.

Quantities of αQ chain variants in heterozygotes with and without a concomitant β‐thalassemia trait

K. Wong, E. Baysal, T. Huisman, 1994 .

Molecular characterization of Hb S(C) beta-thalassemia in American blacks.

A. Kutlar, T. Huisman, V. Mckie, 1991, American journal of hematology.

HB Bibba OR α2136(H19)LEU→PROβ2 in a Caucasian Family from Alabama

J. Prchal, E. Baysal, B. Adler, 1995 .

Binding of nuclear factors to the proximal and distal CACCC motifs of the beta-globin gene promoter: implications for the -101 (C-->T) 'silent' beta-thalassemia mutation.

T. Huisman, E. Baysal, M. L. Ribeiro, 1994, Acta haematologica.

alpha-Thalassaemia in the population of Cyprus.

P. Ioannou, T. Huisman, M. Angastiniotis, 1995, British journal of haematology.

A de novo deletion causing epsilon gamma delta beta-thalassemia in a Dutch patient.

L. Bernini, T. Huisman, N. S. Smetanina, 1996, Acta haematologica.