Literature DB >> 489017

High genetic polymorphism of hemoglobin disorders in Laos. Complex phenotypes due to associated thalassemic syndromes.

D Sicard, Y Lieurzou, C Lapoumeroulie, D Labie.   

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Year:  1979        PMID： 489017     DOI： 10.1007/bf00399399

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  21 in total

1.  Hemoglobin Koya Dora: high frequency of a chain termination mutant.

Authors:  W W De Jong; P Meera Khan; L F Bernini
Journal:  Am J Hum Genet       Date:  1975-01       Impact factor: 11.025

2.  THE COEXISTENCE OF THE GENES FOR HEMOGLOBIN E AND ALPHA-THALASSEMIA IN THAIS, WITH RESULTANT SUPPRESSION OF HEMOGLOBIN E SYNTHESIS.

Authors:  S TUCHINDA; D L RUCKNAGEL; V MINNICH; U BOONYAPRAKOB; K BALANKURA; V SUVATEE
Journal:  Am J Hum Genet       Date:  1964-09       Impact factor: 11.025

3.  [FREQUENCY OF HEMOGLOBIN E IN LAOS].

Authors:  H BAUP
Journal:  Med Trop (Mars)       Date:  1964 Jan-Feb

4.  HEMOGLOBIN HOPE: A BETA CHAIN VARIANT.

Authors:  V MINNICHI; R J HILL; P D KHURI; M E ANDERSON
Journal:  Blood       Date:  1965-05       Impact factor: 22.113

5.  Abnormal functional properties of Hb Hope alpha C2A beta2 (H14) Gly-Asp: a low oxygen affinity hemoglobin with decreased DPG effect.

Authors:  J Thillet; J Caburi; B Brun; M Cohen-Solal; M C Garel; M N Minh; J Rosa
Journal:  FEBS Lett       Date:  1974-10-01       Impact factor: 4.124

6.  Defect in hemoglobin synthesis possibly due to a disturbed association.

Authors:  J Pagnier; H Wajcman; A Labie
Journal:  FEBS Lett       Date:  1974-09-01       Impact factor: 4.124

7.  Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain.

Authors:  P F Milner; J B Clegg; D J Weatherall
Journal:  Lancet       Date:  1971-04-10       Impact factor: 79.321

8.  Evidence for a new haemoglobin chain (zeta-chain).

Authors:  G L Capp; D A Rigas; R T Jones
Journal:  Nature       Date:  1970-10-17       Impact factor: 49.962

9.  The separation of human and animal hemoglobins by isoelectric focusing in polyacrylamide gel.

Authors:  J W Drysdale; P Righetti; H F Bunn
Journal:  Biochim Biophys Acta       Date:  1971-01-19

10.  Studies of the distribution of haemoglobin E, thalassaemias and glucose-6-phosphate dehydrogenase deficiency in north-eastern Thailand.

Authors:  P Wasi; S Na-Nakorn; A Suingdumrong
Journal:  Nature       Date:  1967-04-29       Impact factor: 49.962
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  5 in total

1.  Hemoglobin abnormalities. An evaluation on new-born infants and their mothers in a maternity unit close to Brazzaville (P.R. Congo).

Authors:  M Lallemant; F Galacteros; S Lallemant-Lecoeur; J Feingold; P Carnevale; V Boukila; J Mouchet; J Rosa
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

Review 2.  The thalassemias: molecular mechanisms of human genetic disease.

Authors:  R A Spritz; B G Forget
Journal:  Am J Hum Genet       Date:  1983-05       Impact factor: 11.025

3.  Impairment of the growth of Plasmodium falciparum in HbEE erythrocytes.

Authors:  R L Nagel; C Raventos-Suarez; M E Fabry; H Tanowitz; D Sicard; D Labie
Journal:  J Clin Invest       Date:  1981-07       Impact factor: 14.808

4.  Next-generation sequencing improves thalassemia carrier screening among premarital adults in a high prevalence population: the Dai nationality, China.

Authors:  Jing He; Wenhui Song; Jinlong Yang; Sen Lu; Yuan Yuan; Junfu Guo; Jie Zhang; Kai Ye; Fan Yang; Fangfang Long; Zhiyu Peng; Haijing Yu; Le Cheng; Baosheng Zhu
Journal:  Genet Med       Date:  2017-01-26       Impact factor: 8.822

5.  Interaction-based evolution: how natural selection and nonrandom mutation work together.

Authors:  Adi Livnat
Journal:  Biol Direct       Date:  2013-10-18       Impact factor: 4.540
  5 in total

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