Glicosa-6-fosfatase (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Glicosa-6-fosfatase" in Galician language version.

refsWebsite

Global rank Galician rank

15nih.gov

4^th place

6^th place

12doi.org

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1ebi.ac.uk

5,849^th place

619^th place

1omim.org

4,380^th place

1,519^th place

1biochemj.org

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4,880^th place

1web.archive.org

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1jbc.org

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611^th place

biochemj.org

van Schaftingen E, Gerin I (2002). "The glucose-6-phosphatase system". Biochem. J. 362 (Pt 3): 513–32. PMC 1222414. PMID 11879177. doi:10.1042/0264-6021:3620513.

doi.org

dx.doi.org

Ghosh A, Shieh JJ, Pan CJ, Sun MS, Chou JY (2002). "The catalytic center of glucose-6-phosphatase. HIS176 is the nucleophile forming the phosphohistidine-enzyme intermediate during catalysis". J. Biol. Chem. 277 (36): 32837–42. PMID 12093795. doi:10.1074/jbc.M201853200.
Ghosh A, Shieh JJ, Pan CJ, Chou JY (2004). "Histidine 167 is the phosphate acceptor in glucose-6-phosphatase-beta forming a phosphohistidine enzyme intermediate during catalysis". J. Biol. Chem. 279 (13): 12479–83. PMID 14718531. doi:10.1074/jbc.M313271200.
van Schaftingen E, Gerin I (2002). "The glucose-6-phosphatase system". Biochem. J. 362 (Pt 3): 513–32. PMC 1222414. PMID 11879177. doi:10.1042/0264-6021:3620513.
Pan CJ, Lei KJ, Annabi B, Hemrika W, Chou JY (1998). "Transmembrane topology of glucose-6-phosphatase". J. Biol. Chem. 273 (11): 6144–8. PMID 9497333. doi:10.1074/jbc.273.11.6144. Arquivado dende o orixinal o 30 de maio de 2020. Consultado o 11 de xaneiro de 2014.
Angaroni CJ, de Kremer RD, Argaraña CE; et al. (2004). "Glycogen storage disease type Ia in Argentina: two novel glucose-6-phosphatase mutations affecting protein stability". Mol. Genet. Metab. 83 (3): 276–9. PMID 15542400. doi:10.1016/j.ymgme.2004.06.010.
Chou JY, Jun HS, Mansfield BC (2010). "Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy". Nature Reviews Endocrinology 6 (12): 676–88. PMID 20975743. doi:10.1038/nrendo.2010.189.
Jun HS, Lee YM, Cheung YY; et al. (2010). "Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome". Blood 116 (15): 2783–92. PMC 2974586. PMID 20498302. doi:10.1182/blood-2009-12-258491.
Chou JY, Matern D, Mansfield BC, Chen YT (2002). "Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex". Curr. Mol. Med. 2 (2): 121–43. PMID 11949931. doi:10.2174/1566524024605798.
Froissart R, Piraud M, Boudjemline AM; et al. (2011). "Glucose-6-phosphatase deficiency". Orphanet J Rare Dis 6: 27. PMC 3118311. PMID 21599942. doi:10.1186/1750-1172-6-27.
Jun HS, Lee YM, Song KD, Mansfield BC, Chou JY (2011). "G-CSF improves murine G6PC3-deficient neutrophil function by modulating apoptosis and energy homeostasis". Blood 117 (14): 3881–92. PMC 3083300. PMID 21292774. doi:10.1182/blood-2010-08-302059.
Boztug K, Appaswamy G, Ashikov A; et al. (2009). "A syndrome with congenital neutropenia and mutations in G6PC3". N. Engl. J. Med. 360 (1): 32–43. PMC 2778311. PMID 19118303. doi:10.1056/NEJMoa0805051.
Hayee B, Antonopoulos A, Murphy EJ; et al. (2011). "G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction". Glycobiology 21 (7): 914–24. PMC 3110488. PMID 21385794. doi:10.1093/glycob/cwr023.

ebi.ac.uk

CHEMBL Glucose-6-phosphatase

jbc.org

Pan CJ, Lei KJ, Annabi B, Hemrika W, Chou JY (1998). "Transmembrane topology of glucose-6-phosphatase". J. Biol. Chem. 273 (11): 6144–8. PMID 9497333. doi:10.1074/jbc.273.11.6144. Arquivado dende o orixinal o 30 de maio de 2020. Consultado o 11 de xaneiro de 2014.

nih.gov

ncbi.nlm.nih.gov

Burchell A, Hume R. The glucose-6-phosphatase system in human development. Histol Histopathol. 1995 Oct;10(4):979-93. PMID 8574017. [1]
Ghosh A, Shieh JJ, Pan CJ, Sun MS, Chou JY (2002). "The catalytic center of glucose-6-phosphatase. HIS176 is the nucleophile forming the phosphohistidine-enzyme intermediate during catalysis". J. Biol. Chem. 277 (36): 32837–42. PMID 12093795. doi:10.1074/jbc.M201853200.
Ghosh A, Shieh JJ, Pan CJ, Chou JY (2004). "Histidine 167 is the phosphate acceptor in glucose-6-phosphatase-beta forming a phosphohistidine enzyme intermediate during catalysis". J. Biol. Chem. 279 (13): 12479–83. PMID 14718531. doi:10.1074/jbc.M313271200.
van Schaftingen E, Gerin I (2002). "The glucose-6-phosphatase system". Biochem. J. 362 (Pt 3): 513–32. PMC 1222414. PMID 11879177. doi:10.1042/0264-6021:3620513.
Pan CJ, Lei KJ, Annabi B, Hemrika W, Chou JY (1998). "Transmembrane topology of glucose-6-phosphatase". J. Biol. Chem. 273 (11): 6144–8. PMID 9497333. doi:10.1074/jbc.273.11.6144. Arquivado dende o orixinal o 30 de maio de 2020. Consultado o 11 de xaneiro de 2014.
B Surholt and E A Newsholme. Maximum activities and properties of glucose 6-phosphatase in muscles from vertebrates and invertebrates. Biochem J. 1981 September 15; 198(3): 621–629. [3]
Angaroni CJ, de Kremer RD, Argaraña CE; et al. (2004). "Glycogen storage disease type Ia in Argentina: two novel glucose-6-phosphatase mutations affecting protein stability". Mol. Genet. Metab. 83 (3): 276–9. PMID 15542400. doi:10.1016/j.ymgme.2004.06.010.
Chou JY, Jun HS, Mansfield BC (2010). "Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy". Nature Reviews Endocrinology 6 (12): 676–88. PMID 20975743. doi:10.1038/nrendo.2010.189.
Jun HS, Lee YM, Cheung YY; et al. (2010). "Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome". Blood 116 (15): 2783–92. PMC 2974586. PMID 20498302. doi:10.1182/blood-2009-12-258491.
Pagon RA, Bird TD, Dolan CR; et al. (19 de abril de 2006). "Glycogen Storage Disease Type I." (en inglés). PMID 20301489.
Chou JY, Matern D, Mansfield BC, Chen YT (2002). "Type I glycogen storage diseases: disorders of the glucose-6-phosphatase complex". Curr. Mol. Med. 2 (2): 121–43. PMID 11949931. doi:10.2174/1566524024605798.
Froissart R, Piraud M, Boudjemline AM; et al. (2011). "Glucose-6-phosphatase deficiency". Orphanet J Rare Dis 6: 27. PMC 3118311. PMID 21599942. doi:10.1186/1750-1172-6-27.
Jun HS, Lee YM, Song KD, Mansfield BC, Chou JY (2011). "G-CSF improves murine G6PC3-deficient neutrophil function by modulating apoptosis and energy homeostasis". Blood 117 (14): 3881–92. PMC 3083300. PMID 21292774. doi:10.1182/blood-2010-08-302059.
Boztug K, Appaswamy G, Ashikov A; et al. (2009). "A syndrome with congenital neutropenia and mutations in G6PC3". N. Engl. J. Med. 360 (1): 32–43. PMC 2778311. PMID 19118303. doi:10.1056/NEJMoa0805051.
Hayee B, Antonopoulos A, Murphy EJ; et al. (2011). "G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction". Glycobiology 21 (7): 914–24. PMC 3110488. PMID 21385794. doi:10.1093/glycob/cwr023.

omim.org

OMIM G6PC3 [2]

web.archive.org

Pan CJ, Lei KJ, Annabi B, Hemrika W, Chou JY (1998). "Transmembrane topology of glucose-6-phosphatase". J. Biol. Chem. 273 (11): 6144–8. PMID 9497333. doi:10.1074/jbc.273.11.6144. Arquivado dende o orixinal o 30 de maio de 2020. Consultado o 11 de xaneiro de 2014.