Quantitative analysis of glucose-6-phosphate translocase gene expression in various human tissues and haematopoietic progenitor cells

Journal of Inherited Metabolic Disease

Volumn 23, Issue 6, 2000, Pages 583-592

  Ihara, K ^a   Nomura, A ^a   Hikino, S ^a   Takada, H ^a   Hara, T ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; CARRIER PROTEIN; COMPLEMENTARY DNA; GLUCOSE 6 PHOSPHATE; GLUCOSE 6 PHOSPHATE TRANSLOCASE; POLYPEPTIDE; UNCLASSIFIED DRUG;

ADULT; ARTICLE; BINDING AFFINITY; BRAIN; CONTROLLED STUDY; EXON; FETUS; GENE EXPRESSION; GENETIC ANALYSIS; GLYCOGEN STORAGE DISEASE TYPE 1; HEART; HEMATOPOIETIC CELL; HEPATOMEGALY; HUMAN; HUMAN CELL; HUMAN TISSUE; KIDNEY; KIDNEY HYPERTROPHY; LEUKOCYTE; LIVER; NEUTROPENIA; PRECURSOR CELL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SPLICING; SKELETAL MUSCLE; SYMPTOM; TISSUE SPECIFICITY;

ADOLESCENT; ADULT; AGED; ALTERNATIVE SPLICING; BRAIN; CHILD; FEMALE; FETUS; GENE EXPRESSION; HEMATOPOIETIC STEM CELLS; HUMAN; ISOENZYMES; KIDNEY; LEUKOCYTES; LIVER; MALE; MIDDLE AGE; MUSCLE, SKELETAL; MYOCARDIUM; ORGAN SPECIFICITY; PANCREAS; PHOSPHOTRANSFERASES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA; SUPPORT, NON-U.S. GOV'T;

EID: 0033797364     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005677912539     Document Type: Article

References (22)

1. Neutropenia and impaired neutrophil migration in type 1B glycogen storage disease
2. The molecular basis of the hepatic microsomal glucose-6-phosphatase system
3. Glycogen storage diseases
4. Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type 1b
5. Structure of the gene mutated in glycogen storage disease type 1b
6. A novel method for real time quantitative RT-PCR
7. Defective neutrophil and monocyte functions in glycogen storage disease type 1b: A literature review
8. Real time quantitative PCR
9. Genomic structure of the human glucose-6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type 1b
10. Assignment of the glucose-6-phosphate translocase (G6PT) to human chromosome band 11q23.3 by in situ hybridization
11. Molecular analysis of glycogen storage disease type 1b: Identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11
12. Treatment with lenograstim (glycosylated recombinant human granulocyte colony-stimulating factor) and orthotopic liver transplantation for glycogen storage disease type 1b
13. Type 1b glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system
14. Cloning and characterization of cDNAs encoding a candidate glycogen storage disease type 1b protein in rodents
15. Structure and mutation analysis of the glycogen storage disease type 1b gene
16. In vitro and in vivo effects of granulocyte colony-stimulating factor on neutrophils in glycogen storage disease type 1b: Granulocyte colony-stimulating factor therapy corrects the neutropenia and the defects in respiratory burst activity
17. A different isoform of the transport protein mutated in the glycogen storage disease 1b is expressed in brain
18. Persistence of mutipotent progenitors expressing AML1/ETO transcripts in long-term remission patients with t(8;21) acute myelogenous leukemia
19. A new variant of glycogen storage disease type I probably due to a defect in the glucose-6-phosphate transport system
20. Granulocyte and granulocyte-macrophage colony-stimulating factors for treatment of neutropenia in glycogen storage disease type 1b
21. A gene on chromosome 11q23 coding for a putative glucose-6-phosphate translocase is mutated in glycogen-storage disease types 1b and 1c
22. The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a