PMID: 2699473DOI: 10.3109/03630268908998845Jan 1, 1989Paper

Alpha thalassemia.

Hemoglobin
S A Liebhaber

Abstract

No abstract listed.

References

Supersaturation in sickle cell hemoglobin solutions

Sep 1, 1976·Proceedings of the National Academy of Sciences of the United States of America·J HofrichterW A Eaton

Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene

Aug 11, 1979·Lancet·D R HiggsG R Serjeant

Gelation of sickle cell hemoglobin in mixtures with normal adult and fetal hemoglobins

Oct 9, 1979·Journal of Molecular Biology·H R SunshineW A Eaton

Human embryonic haemoglobins Gower 1 and Gower 2

Jul 12, 1979·Nature·R E GaleE R Huehns

Acquired haemoglobin H disease in leukemia: pathophysiology and molecular basis

Mar 1, 1978·British Journal of Haematology·D J WeatherallM J Lewis

Chromosomal localization of human beta globin gene on human chromosome 11 in somatic cell hybrids

Mar 1, 1978·Proceedings of the National Academy of Sciences of the United States of America·A DeisserothF H Ruddle

The duplicated human alpha globin genes lie close together in cellular DNA

Dec 1, 1978·Proceedings of the National Academy of Sciences of the United States of America·S H Orkin

13C NMR quantitation of polymer in deoxyhemoglobin S gels

Oct 1, 1979·Proceedings of the National Academy of Sciences of the United States of America·C T NoguchiA N Schechter

Precise localization of human beta-globin gene complex on chromosome 11

Oct 1, 1979·Proceedings of the National Academy of Sciences of the United States of America·J GusellaD Housman

Sickle cell anemia as a syndrome: a review of diagnostic features

Jan 1, 1979·American Journal of Hematology·T H Huisman

Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes

Jun 1, 1979·The Journal of Clinical Investigation·S H EmburyY W Kan

alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia

Aug 16, 1979·Nature·A M DozyH M Koenig

The association of sickle cell anemia with heterozygous and homozygous alpha-thalassemia-2: in vitro HB chain synthesis

Jan 1, 1979·American Journal of Hematology·A E FeliceT H Huisman

Modification of hemoglobin H disease by sickle trait

Oct 1, 1979·The Journal of Clinical Investigation·K K MatthayD F Bainton

Localization of the human alpha-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay

Sep 1, 1977·Cell·A DeisserothR Kucherlapati

Differences in affinity of variant beta chains for alpha chains: a possible explanation for the variation in the percentages of beta chain variants in heterozygotes

Jan 1, 1977·Hemoglobin·E C Abraham, T H Huisman

Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome

Apr 1, 1978·The Journal of Pediatrics·G R HonigL N Vida

Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletion

Jul 27, 1978·The New England Journal of Medicine·S H OrkinD G Nathan

Restriction endonuclease analysis of human globin genes in cellular DNA

Aug 14, 1978·Biochemical and Biophysical Research Communications·S SurreyE Schwartz

Competition of normal beta chains and sickle haemoglobin beta chains for alpha chains as a post-translational control mechanism

Dec 7, 1978·Nature·J R ShaefferH F Bunn

Energy reserve and cation composition of irreversibly sickled cells in vivo

Dec 1, 1978·British Journal of Haematology·B E GladerD G Nathan

Trimodality in the percentages of beta chain variants in heterozygotes: the effect of the number of active Hbalpha structural loci

Jan 1, 1977·Hemoglobin·T H Huisman

Identification of a nondeletion defect in alpha-thalassemia

Nov 17, 1977·The New England Journal of Medicine·Y W KanD Todd

Studies of the proporation and synthesis of haemoblogin C Philadelphia in red cells of heterozygotes, a homozygote, and a heterozygote for both haemoglobin G and alpha thalassaemia

Oct 1, 1976·British Journal of Haematology·P F Milner, T H Huisman

Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains

Mar 1, 1976·Proceedings of the National Academy of Sciences of the United States of America·M Seid-AkhavanD L Rucknagel

Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain loci

Oct 11, 1976·Proceedings of the National Academy of Sciences of the United States of America·R M BaineJ G Adams

The interaction of alpha-thalassaemia and haemoglobin G Philadelphia

Feb 1, 1976·British Journal of Haematology·R F RiederD L Rucknagel

The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia

Apr 1, 1986·American Journal of Hematology·P F MilnerJ T Wilson

Alpha thalassaemia and the haematology of normal Jamaican children

Jan 1, 1985·Clinical and Laboratory Haematology·G H MaudeG R Serjeant

Cation depletion by the sodium pump in red cells with pathologic cation leaks. Sickle cells and xerocytes

Dec 1, 1986·The Journal of Clinical Investigation·C H JoinerS E Lux

Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia

Aug 1, 1987·American Journal of Hematology·A E FeliceV C McKie

Molecular screening for haemoglobin constant spring.

May 6, 1989·Lancet·Y E HsiaN S Ching

The influence of fetal hemoglobin on the clinical expression of sickle cell anemia.

Jan 1, 1989·Annals of the New York Academy of Sciences·D R PowarsW A Schroeder

Haemoglobin switching in human embryos: asynchrony of zeta----alpha and epsilon----gamma-globin switches in primitive and definite erythropoietic lineage

Jan 17, 1985·Nature·C PeschleM Marinucci

Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin type

Apr 4, 1985·The New England Journal of Medicine·R L NagelD Labie

Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease

May 1, 1985·The Journal of Clinical Investigation·C T NoguchiA N Schechter

Allele-specific enzymatic amplification of beta-globin genomic DNA for diagnosis of sickle cell anemia.

Apr 1, 1989·Proceedings of the National Academy of Sciences of the United States of America·D Y WuR B Wallace

Hematologic changes in alpha-thalassemia

Aug 1, 1988·American Journal of Clinical Pathology·S FucharoenP Winichagoon

A simple sensitive prenatal test for hydrops fetalis caused by alpha-thalassaemia

Jan 12, 1985·Lancet·E M Rubin, Y W Kan

High resolution gene mapping of the human alpha globin locus.

Jan 1, 1987·Journal of Medical Genetics·R D NichollsD R Higgs

HB Q-Thailand-HB H disease in a Chinese living in Geneva, Switzerland: characterization of the variant and identification of the two alpha-thalassemic chromosomes.

Apr 1, 1987·American Journal of Hematology·P BerisT H Huisman

The primate alpha-globin gene family: a paradigm of the fluid genome.

Jan 1, 1986·Cold Spring Harbor Symposia on Quantitative Biology·J MarksC K Shen

Correlation of clinical phenotype to genotype in haemoglobin H disease.

Feb 27, 1988·Lancet·C KattamisA Metaxotou-Mavrommati

A large deletion encompassing the entire alpha-like globin gene cluster in a family of northern European extraction

Dec 9, 1988·Nucleic Acids Research·P FortinaS Surrey

Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysis

Jan 1, 1988·Hemoglobin·L OggianoM Longinotti

Locus assignment of alpha-globin structural mutations by hybrid-selected translation.

Jan 1, 1985·The Journal of Clinical Investigation·S A Liebhaber, F E Cash

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16.

Oct 10, 1985·Nature·S T ReedersD J Weatherall

Recombination within the human embryonic xi-globin locus: a common xi-xi chromosome produced by gene conversion of the psi xi gene.

Oct 1, 1985·Cell·A V HillD R Higgs

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

Dec 20, 1985·Science·R K SaikiN Arnheim

Molecular defects in 2 examples of severe Hb H disease.

Mar 1, 1986·Scandinavian Journal of Haematology·R J TrentH Kronenberg

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Citations

The switch from fetal to adult erythropoiesis

Sep 15, 2000·Clinics in Perinatology·C Dame, S E Juul

Homozygous frameshift mutation in the SLC22A12 gene in a patient with primary gout and high levels of serum uric acid

Jul 31, 2007·Journal of Clinical Pathology·J Vázquez-MelladoS A Cuevas-Covarrubias

A laboratory strategy for genotyping haemoglobin H disease in the Chinese

Oct 5, 2006·Journal of Clinical Pathology·Amy Yuk-Yin ChanLi-Chong Chan

Active stabilization of human endothelial nitric oxide synthase mRNA by hnRNP E1 protects against antisense RNA and microRNAs

Mar 13, 2013·Molecular and Cellular Biology·J J David HoPhilip A Marsden

History and current status of newborn screening for hemoglobinopathies

Mar 9, 2010·Seminars in Perinatology·Jane M Benson, Bradford L Therrell

Molecular genetic studies in black families with sickle cell anemia and unusually high levels of fetal hemoglobin

Jan 1, 1992·Hemoglobin·W K SeltzerJ H Githens

The possible role of genetic modifiers in the clinical severity of sickle cell syndromes

Jan 1, 1989·Annals of the New York Academy of Sciences·S Piomelli

Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin gene

Jan 17, 2002·Hemoglobin·J S WayeD H Chui

Hb H disease among Tunisians: molecular characterization of alpha-thalassemia determinants and hematological findings

Feb 27, 2003·Hemoglobin·Amine ZoraiKousay Dellagi

The nondeletional types of Hb H disease in Guangxi

Jan 1, 1992·Hemoglobin·X J WenW X Lin

A novel alpha-thalassemia-2 (-2.7-kb) observed in a Chinese patient with Hb H disease

Nov 1, 1991·American Journal of Hematology·J B ZhaoT H Huisman

A new alpha alpha alpha anti-3.7 alpha-globin allele

Nov 1, 1994·Hemoglobin·Z H Lu, M H Steinberg

Postnatal changes in the quantities of globin chains and hemoglobin types in two babies with Hb H disease

Jan 1, 1993·American Journal of Hematology·K M McKieT H Huisman

Expression and developmental control of the human alpha-globin gene cluster

Jul 21, 1998·Annals of the New York Academy of Sciences·S A Liebhaber, J E Russell

Regarding Luecke T, Pfister S, Duerken M. Neurodevelopmental outcome and haematological course of a long-time survivor with homozygous alpha-thalassaemia: case report and review of the literature. Acta Paediatr 2005;94:1330-3

Aug 3, 2006·Acta Paediatrica·Roswitha Dickerhoff

Detection of deletions/duplications in α-globin gene cluster by multiplex ligation-dependent probe amplification

Jun 27, 2012·Genetic Testing and Molecular Biomarkers·Naghmeh Nezhat, Mohammad Taghi Akbari

Rapid detection of -alpha 4.2 deletion of alpha-thalassemia-2 by polymerase chain reaction

Oct 1, 1994·Annals of Hematology·J G ChangC P Lin

An mRNA stability complex functions with poly(A)-binding protein to stabilize mRNA in vitro.

Jun 22, 1999·Molecular and Cellular Biology·Z WangM Kiledjian

Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 cases

Sep 18, 2001·American Journal of Hematology·J S WayeD H Chui

Detection of a small novel deletion in the alpha-globin gene and type II-alpha(3.7) deletion by heteroduplex formation

Oct 31, 2002·Hemoglobin·Amy Yuk-Yin ChanLi Chong Chan

Detection of α-Thalassemia by Using Multiplex Ligation-Dependent Probe Amplification as an Additional Method for Rare Mutations in Southern Turkey

Nov 5, 2016·Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion·Ozge Ozalp YuregirTugce B Balci

Thalassemia: genotypes and phenotypes

May 1, 1991·Annals of Hematology·D Loukopoulos

Hb Fukuyama or alpha 2 beta(2)77(EF1)His----Tyr observed in an Indonesian female

Jan 1, 1991·Hemoglobin·J W SmitT H Huisman

Alpha alpha alpha alpha anti-3.7 type II: a new alpha-globin gene rearrangement suggesting that the alpha-globin gene duplication could be caused by intrachromosomal recombination

Apr 1, 1992·Human Genetics·M De AngiolettiC Carestia

Molecular basis of alpha-thalassemia in Portugal

Jan 1, 1995·Hemoglobin·M J PeresJ Lavinha

Hb F in sickle cell anemia

Jan 15, 1993·Experientia·A D Adekile, T H Huisman

Hemoglobin disorders in Macao

May 1, 1997·Hemoglobin·M L Ribeiro, G P Tamagnini

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

Jul 1, 1994·American Journal of Hematology·E Baysal, T H Huisman

Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin gene

Mar 11, 1998·Hemoglobin·E PagliettiR Galanello

Polycythaemia and microcytosis arising from the combination of a new high oxygen affinity haemoglobin (Hb luton, alpha 89 His-->Leu) and alpha thalassaemia trait

Nov 1, 1992·British Journal of Haematology·D WilliamsonS C Davies

DNA polymorphisms associated with Hb D-Los Angeles [beta 121(GH4)Glu-->Gln] in southern Italy

Feb 1, 1993·Hemoglobin·G FiorettiC Carestia

Molecular characterization of a new family with alpha-thalassemia-1 (--MA mutation)

Aug 1, 1995·American Journal of Hematology·A VillegasM Lozano

Chicken Egg Yolk Antibodies Specific for the γ Chain of Human Hemoglobin for Diagnosis of Thalassemia

Jun 1, 2006·International Journal of Hematology·Pornrutsami JintaridthWatchara Kasinrerk

Thalassemia: genotypes and phenotypes

Apr 1, 1991·Annals of Hematology·D Loukopoulos

A new gene deletion involving the alpha 2-, alpha 1-, and theta 1-globin genes in a black family with Hb H disease

Apr 1, 1992·American Journal of Hematology·Y J FeiT H Huisman

Detection of the (--SEA) double alpha-globin gene deletion by a simple immunologic assay for embryonic zeta-globin chains

Sep 1, 1993·American Journal of Hematology·J H IrelandY E Hsia

A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian family

Aug 1, 1991·British Journal of Haematology·P FortinaC Camaschella

Detection of the Hb Quong Sze mutation in a Chinese family by selective amplification of the alpha 2-globin gene and restriction map analysis with Msp I

Jan 1, 1991·Hemoglobin·S LiangW X Lin

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

Sep 1, 1993·British Journal of Haematology·M A CürükT H Huisman

Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin gene.

Jan 1, 1990·Hemoglobin·W ZhaoT H Huisman

Hb Bart's levels in cord blood and alpha-thalassemia mutations in Cyprus

Sep 7, 2000·Hemoglobin·K KyriacouM Kleanthous

Homozygous Hb Sallanches [alpha104(G11)Cys-->Tyr] in a Pakistani child with Hb H disease

Feb 24, 2001·Hemoglobin·J S WayeM Kirby

Lethal alpha-thalassaemia created by gene targeting in mice and its genetic rescue

Sep 1, 1995·Nature Genetics·C PásztyE M Rubin

Chicken egg yolk antibodies specific for the gamma chain of human hemoglobin for diagnosis of thalassemia

Jun 22, 2006·International Journal of Hematology·Pornrutsami JintaridthWatchara Kasinrerk

Human alpha-globin genes demonstrate autonomous developmental regulation in transgenic mice.

Jul 1, 1991·Molecular and Cellular Biology·M AlbitarS A Liebhaber

Developmental silencing of the embryonic zeta-globin gene: concerted action of the promoter and the 3'-flanking region combined with stage-specific silencing by the transcribed segment.

Jun 1, 1996·Molecular and Cellular Biology·S A LiebhaberJ E Russell

Differential diagnosis and management of anemia in the newborn

Jul 28, 2004·Pediatric Clinics of North America·Matthew J BizzarroRichard A Ehrenkranz

Neonatal anemia

Apr 16, 2008·Seminars in Fetal & Neonatal Medicine·Sanjay AherSandeep Kadam

Clinical and genetic characteristics of hemoglobin H disease in Iran.

Dec 25, 2021·Pediatric Hematology and Oncology·Hassan AbolghasemiSamin Alavi

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