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The Small Heat Shock-related Protein, HSP20, Is Phosphorylated on Serine 16 during Cyclic Nucleotide-dependent Relaxation

The Journal of biological chemistry, 1999-04, Vol.274 (16), p.11344-11351

1999

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Clinical and Genetic Heterogeneity in Black Patients With Homozygous β-Thalassemia From the Southeastern United States

Blood, 1988-09, Vol.72 (3), p.1007-1014

1988

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Mild and Severe β-Thalassemia Among Homozygotes From Turkey: Identification of the Types by Hybridization of Amplified DNA With Synthetic Probes

Blood, 1988-01, Vol.71 (1), p.248-251

1988

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A C → T substitution at nt ― 101 in a conserved DNA sequence of the promotor region of the β-globin gene is associated with silent β-thalassemia

Blood, 1989-05, Vol.73 (6), p.1705-1711

1989

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α and β thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization

British journal of haematology, 1994-02, Vol.86 (2), p.351-354

1994

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β-Thalassemia in Turkey

Hemoglobin, 1990, Vol.14 (1), p.1-13

1990

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Chromosomal Mapping of the Human CNP Gene Using a Meiotic Crossover DNA Panel, PCR, and Allele-Specific Probes

Genomics (San Diego, Calif.), 1993-05, Vol.16 (2), p.542-545

1993

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β-thalassemia due to A T→A mutation within the ATA box

Biochemical and biophysical research communications, 1988-06, Vol.153 (2), p.741-747

1988

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Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia

Hemoglobin, 1992, Vol.16 (1-2), p.51-66

1992

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Molecular identification of hereditary persistence of fetal hemoglobin type 2 (HPFH type 2) in patients from Brazil

Annals of hematology, 1995-03, Vol.70 (3), p.159-161

1995

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Hb S(C)‐β+‐thalassaemia: different mutations are associated with different levels of normal Hb A

British journal of haematology, 1988-09, Vol.70 (1), p.85-89

1988

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

Blood, 1990-11, Vol.76 (9), p.1896-1897

1990

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β-Thalassemia in Yugoslavia

Hemoglobin, 1990, Vol.14 (1), p.15-24

1990

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

British journal of haematology, 1988-03, Vol.68 (3), p.351-355

1988

Volltextzugriff (PDF)

Metabolic formation of 1,9,10-trihydroxy-9,10-dihydro-3-methylcholanthrene: a potential proximate carcinogen from 3-methylcholanthrene

Journal of the American Chemical Society, 1978-01, Vol.100 (2), p.645-647

1978

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High Frequencies of a Rearrangement (+ATA; -T) at -530 to the β-Globin Gene in Different Populations Indicate the Absence of a Correlation with a Silent β-Thalassemia Determinant

Hemoglobin, 1989, Vol.13 (1), p.1-5

1989

Volltextzugriff (PDF)

Association of Hb santa ANA [α2β288(F4)LEU→PRO] And Hb porto alegre [α2β29(A6)SER→CYS] in a brazilian female

Hemoglobin, 1994, Vol.18 (3), p.235-239

1994

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The metabolism of 3-methylcholanthrene by liver and lung microsomes: Effect of enzyme inducing agents

Cancer letters, 1983-10, Vol.20 (3), p.323-331

1983

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Gas Chromatographic Assay of Epoxide Hydrase Activity with 3-Methylcholanthrene-11,12-Oxide

Science (American Association for the Advancement of Science), 1973-09, Vol.181 (4103), p.951-952

1973

Volltextzugriff (PDF)

The metabolism of 1-hydroxy- and 2-hydroxy-3-methylcholanthrene by liver microsomes: Effect of enzyme inducing agents

Cancer letters, 1984-08, Vol.24 (1), p.103-110

1984

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Hepatic epoxide hydrase in neonatal and partially hepatectomized rats

Cancer research (Chicago, Ill.), 1974-10, Vol.34 (10), p.2810-2813

1974

Volltextzugriff (PDF)

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

British journal of haematology, 1989-05, Vol.72 (1), p.73-80

1989

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Chinese in West Malaysia : the geography of beta thalassaemia mutations

Singapore medical journal, 1990-08, Vol.31 (4), p.374-377

1990

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An Initiation Codon Mutation as a Cause of a β-Thalassemia

Hemoglobin, 1990, Vol.14 (2), p.169-176

1990

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

Biochimica et biophysica acta, 1988-01, Vol.949 (1), p.43-48

1988

Volltextzugriff (PDF)

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The Small Heat Shock-related Protein, HSP20, Is Phosphorylated on Serine 16 during Cyclic Nucleotide-dependent Relaxation

Clinical and Genetic Heterogeneity in Black Patients With Homozygous β-Thalassemia From the Southeastern United States

Mild and Severe β-Thalassemia Among Homozygotes From Turkey: Identification of the Types by Hybridization of Amplified DNA With Synthetic Probes

A C → T substitution at nt ― 101 in a conserved DNA sequence of the promotor region of the β-globin gene is associated with silent β-thalassemia

α and β thalassaemia among Chinese children in Guangxi Province, P.R. China: molecular and haematological characterization

β-Thalassemia in Turkey

Chromosomal Mapping of the Human CNP Gene Using a Meiotic Crossover DNA Panel, PCR, and Allele-Specific Probes

β-thalassemia due to A T→A mutation within the ATA box

Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia

Molecular identification of hereditary persistence of fetal hemoglobin type 2 (HPFH type 2) in patients from Brazil

Hb S(C)‐β+‐thalassaemia: different mutations are associated with different levels of normal Hb A

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

β-Thalassemia in Yugoslavia

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

Metabolic formation of 1,9,10-trihydroxy-9,10-dihydro-3-methylcholanthrene: a potential proximate carcinogen from 3-methylcholanthrene

High Frequencies of a Rearrangement (+ATA; -T) at -530 to the β-Globin Gene in Different Populations Indicate the Absence of a Correlation with a Silent β-Thalassemia Determinant

Association of Hb santa ANA [α2β288(F4)LEU→PRO] And Hb porto alegre [α2β29(A6)SER→CYS] in a brazilian female

The metabolism of 3-methylcholanthrene by liver and lung microsomes: Effect of enzyme inducing agents

Gas Chromatographic Assay of Epoxide Hydrase Activity with 3-Methylcholanthrene-11,12-Oxide

The metabolism of 1-hydroxy- and 2-hydroxy-3-methylcholanthrene by liver microsomes: Effect of enzyme inducing agents

Hepatic epoxide hydrase in neonatal and partially hepatectomized rats

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

Chinese in West Malaysia : the geography of beta thalassaemia mutations

An Initiation Codon Mutation as a Cause of a β-Thalassemia

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

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