赤血球酵素異常症
English Journal
- Erythrocytic pyruvate kinase mutations causing hemolytic anemia, osteosclerosis, and seconday hemochromatosis in dogs.
- Gultekin GI, Raj K, Foureman P, Lehman S, Manhart K, Abdulmalik O, Giger U.SourceSection of Medical Genetics, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA.
- Journal of veterinary internal medicine / American College of Veterinary Internal Medicine.J Vet Intern Med.2012 Jul-Aug;26(4):935-44.
- BACKGROUND: Erythrocytic pyruvate kinase (PK) deficiency, first documented in Basenjis, is the most common inherited erythroenzymopathy in dogs.OBJECTIVES: To report 3 new breed-specific PK-LR gene mutations and a retrospective survey of PK mutations in as mall and selected group of Beagles and West
- PMID 22805166
- Glucose-6-phosphate isomerase deficiency results in mTOR activation, failed translocation of lipin 1α to the nucleus and hypersensitivity to glucose: Implications for the inherited glycolytic disease.
- Haller JF, Krawczyk SA, Gostilovitch L, Corkey BE, Zoeller RA.SourceDepartment of Physiology and Biophysics, Boston University School of Medicine, USA.
- Biochimica et biophysica acta.Biochim Biophys Acta.2011 Nov;1812(11):1393-402. doi: 10.1016/j.bbadis.2011.07.007. Epub 2011 Jul 21.
- Inherited glucose-6-phosphate isomerase (GPI) deficiency is the second most frequent glycolytic erythroenzymopathy in humans. Patients present with non-spherocytic anemia of variable severity and with neuromuscular dysfunction. We previously described Chinese hamster (CHO) cell lines with mutations
- PMID 21787864
- A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil.
- Oliveira RA, Oshiro M, Hirata MH, Hirata RD, Ribeiro GS, Medeiros TM, de O Barretto OC.SourceDepartamento de Farmácia, Universidade Federal do Maranhão, São Luis, MA Brazil.
- Genetics and molecular biology.Genet Mol Biol.2009 Apr;32(2):251-4. doi: 10.1590/S1415-47572009005000033. Epub 2009 Jun 1.
- In this study, we used red cell glucose-6-phosphate dehydrogenase (G6PD) activity to screen for G6PD-deficient individuals in 373 unrelated asymptomatic adult men who were working with insecticides (organophosphorus and carbamate) in dengue prevention programs in 27 cities in São Paulo State, Brazi
- PMID 21637675
Japanese Journal
- 遺伝性球状赤血球症を他の溶血性貧血から識別するための鑑別検査
- 日本におけるグルコース-6-リン酸脱水素酵素異常症
- Real-time PCR genotyping assay for feline erythrocyte pyruvate kinase deficiency and mutant allele frequency in purebred cats in Japan
Related Links
- PK deficiency is the most common erythroenzymopathy associated with hereditary non-spherocytic hemolytic anemia due to a glycolytic enzyme defect. We determined three mutations (664-6 ins GAC, 1468T, 1436A) by the ...
- programs in 27 cities in São Paulo State, Brazil. Twenty-one unrelated male children suspected of having erythroenzymopathy who were attended at hospitals in São Paulo city were also studied. Fifteen of the 373 ...
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- 英
- erythroenzymopathy, red blood cell enzymopathy, red cell enzyme abnormalities