Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.
about
The effect of alpha+-thalassaemia on the incidence of malaria and other diseases in children living on the coast of Kenyaα-thalassaemiaHigh-speed shaking of frozen blood clots for extraction of human and malaria parasite DNA.Distribution of alpha thalassaemia gene variants in diverse ethnic populations in malaysia: data from the institute for medical research.Nutritional status of young children with inherited blood disorders in western Kenya.Heritability of the human infectious reservoir of malaria parasitesAlpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population.Molecular characterization of α- and β-thalassaemia among Malay patients.The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.A mechanism of ineffective erythropoiesis in β-thalassemia/Hb E diseaseSpecific receptor usage in Plasmodium falciparum cytoadherence is associated with disease outcome.A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand.High prevalence of alpha- and beta-thalassemia in the Kadazandusuns in East Malaysia: challenges in providing effective health care for an indigenous group.HbD Punjab/HbQ India Compound Heterozygosity: An Unusual Association.An assessment of the impact of host polymorphisms on Plasmodium falciparum var gene expression patterns among Kenyan childrenProcesses of copy-number change in human DNA: the dynamics of {alpha}-globin gene deletion.Cytokine profiles at birth predict malaria severity during infancy.Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong KongA human complement receptor 1 polymorphism that reduces Plasmodium falciparum rosetting confers protection against severe malaria.α-Thalassemia associated with hb instability: a tale of two features. the case of Hb Rogliano or α1 Cod 108(G15)Thr→Asn and Hb Policoro or α2 Cod 124(H7)Ser→ProInvestigating alpha-globin structural variants: a retrospective review of 135,000 Brazilian individualsCo-inheritance of alpha+-thalassaemia and sickle trait results in specific effects on haematological parametersMechanistic Studies of the Negative Epistatic Malaria-protective Interaction Between Sickle Cell Trait and α(+)thalassemiaNine unknown rearrangements in 16p13.3 and 11p15.4 causing alpha- and beta-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification.Rapid, accurate genotyping of the common -alpha(4.2) thalassaemia deletion based on the use of denaturing HPLCCompound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)(0)-thalassemia in eastern India.API2-MALT1 fusion transcripts involved in mucosa-associated lymphoid tissue lymphoma: multiplex RT-PCR detection using formalin-fixed paraffin-embedded specimensA comparative study of hematological parameters of α and β thalassemias in a high prevalence zone: Saudi Arabia.Development and validation of a high throughput, closed tube method for the determination of haemoglobin alpha gene (HBA1 and HBA2) numbers by gene ratio assay copy enumeration-PCR (GRACE-PCR).Hemoglobin E Prevalence among Ethnic Groups Residing in Malaria-Endemic Areas of Northern Thailand and Its Lack of Association with Plasmodium falciparum Invasion In Vitro.Inheritance of Hereditary Persistence of Fetal Haemoglobin (HPFH) in a Family of Western Odisha, IndiaMalaria and Age Variably but Critically Control Hepcidin Throughout Childhood in Kenya.Inherited hemoglobin disorders in an Afro-Amazonian community: SaracuraSickle cell disease: acute clinical manifestations in early childhood and molecular characteristics in a group of children in Rio de JaneiroEMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.Co-inheritance of sickle cell trait and thalassemia mutations in South central iranMutation screening for thalassaemia in the Jino ethnic minority population of Yunnan Province, Southwest China.Negative epistasis between the malaria-protective effects of alpha+-thalassemia and the sickle cell trait.Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic HybridizationHBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotype.
P2860
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P2860
Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.
description
2000 nî lūn-bûn
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2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
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2000年學術文章
@zh-hant
name
Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.
@en
type
label
Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.
@en
prefLabel
Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.
@en
P2093
P1433
P1476
Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.
@en
P2093
P304
P407
P577
2000-01-01T00:00:00Z