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Literature DB >> 5870194

Hereditary ovalocytosis and haemoglobin E-ovalocytosis in Malayan aborigines.

L I Eng.

Abstract

Entities: Disease

Mesh：

Substances：
Hemoglobins, Abnormal

Year: 1965 PMID： 5870194 DOI： 10.1038/2081329a0

Source DB: PubMed Journal: Nature ISSN： 0028-0836 Impact factor: 49.962

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Cited

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7 in total

1. High prevalence of Southeast Asian ovalocytosis in Malays with distal renal tubular acidosis.

Authors: Narazah Mohd Yusoff; Hans Van Rostenberghe; Taku Shirakawa; Kaoru Nishiyama; Noryati Amin; Zainal Darus; Nik Zainal; Nizam Isa; Hiroyuki Nozu; Masafumi Matsuo
Journal: J Hum Genet Date: 2003-11-15 Impact factor: 3.172

2. Erythrocyte β spectrin can be genetically targeted to protect mice from malaria.

Authors: Patrick M Lelliott; Hong Ming Huang; Matthew W Dixon; Arman Namvar; Adam J Blanch; Vijay Rajagopal; Leann Tilley; Cevayir Coban; Brendan J McMorran; Simon J Foote; Gaetan Burgio
Journal: Blood Adv Date: 2017-12-12

3. Glucose-6-phosphate dehydrogenase deficiency and Southeast Asian ovalocytosis in asymptomatic Plasmodium carriers in Sumba island, Indonesia.

Authors: Hana Shimizu; Moedrik Tamam; Augustinus Soemantri; Takafumi Ishida
Journal: J Hum Genet Date: 2005-07-30 Impact factor: 3.172

Review 4. The Peopling and Migration History of the Natives in Peninsular Malaysia and Borneo: A Glimpse on the Studies Over the Past 100 years.

Authors: Boon-Peng Hoh; Lian Deng; Shuhua Xu
Journal: Front Genet Date: 2022-01-27 Impact factor: 4.599

Hereditary ovalocytosis and haemoglobin E-ovalocytosis in Malayan aborigines.

1. High prevalence of Southeast Asian ovalocytosis in Malays with distal renal tubular acidosis.

2. Erythrocyte β spectrin can be genetically targeted to protect mice from malaria.

3. Glucose-6-phosphate dehydrogenase deficiency and Southeast Asian ovalocytosis in asymptomatic Plasmodium carriers in Sumba island, Indonesia.

Review 4. The Peopling and Migration History of the Natives in Peninsular Malaysia and Borneo: A Glimpse on the Studies Over the Past 100 years.

5. Trafficking defects of the Southeast Asian ovalocytosis deletion mutant of anion exchanger 1 membrane proteins.

6. The mode of inheritance of ovalocytosis/elliptocytosis in Malaysian Orang Asli families.

7. Accurate light microscopic diagnosis of South-East Asian ovalocytosis.