GLUD1 (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "GLUD1" in Galician language version.

refsWebsite

Global rank Galician rank

15nih.gov

4^th place

6^th place

13doi.org

2^nd place

7^th place

2archive.org

6^th place

8^th place

1web.archive.org

1^st place

1jbc.org

4,455^th place

611^th place

archive.org (Global: 6^th place; Galician: 8^th place)

Pinney SE, MacMullen C, Becker S, Lin YW, Hanna C, Thornton P, Ganguly A, Shyng SL, Stanley CA (agosto de 2008). "Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations". The Journal of Clinical Investigation 118 (8): 2877–86. PMC 2441858. PMID 18596924. doi:10.1172/JCI35414.
Højlund K, Hansen T, Lajer M, Henriksen JE, Levin K, Lindholm J, Pedersen O, Beck-Nielsen H (xuño de 2004). "A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene". Diabetes 53 (6): 1592–8. PMID 15161766. doi:10.2337/diabetes.53.6.1592.

doi.org (Global: 2^nd place; Galician: 7^th place)

dx.doi.org

Shashidharan P, Michaelidis TM, Robakis NK, Kresovali A, Papamatheakis J, Plaitakis A (xuño de 1994). "Novel human glutamate dehydrogenase expressed in neural and testicular tissues and encoded by an X-linked intronless gene". J. Biol. Chem. 269 (24): 16971–6. PMID 8207021. doi:10.1016/S0021-9258(19)89484-X. Arquivado dende o orixinal o 29 de setembro de 2007. Consultado o 01 de xaneiro de 2022.
Smith TJ, Schmidt T, Fang J, Wu J, Siuzdak G, Stanley CA (maio de 2002). "The structure of apo human glutamate dehydrogenase details subunit communication and allostery". J. Mol. Biol. 318 (3): 765–77. PMID 12054821. doi:10.1016/S0022-2836(02)00161-4.
Banerjee S, Schmidt T, Fang J, Stanley CA, Smith TJ (abril de 2003). "Structural studies on ADP activation of mammalian glutamate dehydrogenase and the evolution of regulation". Biochemistry 42 (12): 3446–56. PMID 12653548. doi:10.1021/bi0206917.
Smith TJ, Peterson PE, Schmidt T, Fang J, Stanley CA (marzo de 2001). "Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation". J. Mol. Biol. 307 (2): 707–20. PMID 11254391. doi:10.1006/jmbi.2001.4499.
Peterson PE, Smith TJ (xullo de 1999). "The structure of bovine glutamate dehydrogenase provides insights into the mechanism of allostery". Structure 7 (7): 769–82. PMID 10425679. doi:10.1016/S0969-2126(99)80101-4.
George A, Bell JE (decembro de 1980). "Effects of adenosine 5'-diphosphate on bovine glutamate dehydrogenase: diethyl pyrocarbonate modification". Biochemistry 19 (26): 6057–61. PMID 7470450. doi:10.1021/bi00567a017.
Fang, J; Hsu, BY; MacMullen, CM; Poncz, M; Smith, TJ; Stanley, CA (2002). "Expression, purification and characterization of GLUD1 allosteric regulatory mutations". Biochem. J. 363 (Pt 1): 81–7. PMC 1222454. PMID 11903050. doi:10.1042/0264-6021:3630081.
Won JG, Tseng HS, Yang AH, Tang KT, Jap TS, Lee CH, Lin HD, Burcus N, Pittenger G, Vinik A (novembro de 2006). "Clinical features and morphological characterization of 10 patients with noninsulinoma pancreatogenous hypoglycaemia syndrome (NIPHS)". Clinical Endocrinology 65 (5): 566–78. PMID 17054456. doi:10.1111/j.1365-2265.2006.02629.x.
Pinney SE, MacMullen C, Becker S, Lin YW, Hanna C, Thornton P, Ganguly A, Shyng SL, Stanley CA (agosto de 2008). "Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations". The Journal of Clinical Investigation 118 (8): 2877–86. PMC 2441858. PMID 18596924. doi:10.1172/JCI35414.
Glaser B, Blech I, Krakinovsky Y, Ekstein J, Gillis D, Mazor-Aronovitch K, Landau H, Abeliovich D (outubro de 2011). "ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia". Genetics in Medicine 13 (10): 891–4. PMID 21716120. doi:10.1097/GIM.0b013e31821fea33.
Højlund K, Hansen T, Lajer M, Henriksen JE, Levin K, Lindholm J, Pedersen O, Beck-Nielsen H (xuño de 2004). "A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene". Diabetes 53 (6): 1592–8. PMID 15161766. doi:10.2337/diabetes.53.6.1592.
Mazor-Aronovitch K, Gillis D, Lobel D, Hirsch HJ, Pinhas-Hamiel O, Modan-Moses D, Glaser B, Landau H (outubro de 2007). "Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism". European Journal of Endocrinology 157 (4): 491–7. PMID 17893264. doi:10.1530/EJE-07-0445.
Stanley CA, Thornton PS, Ganguly A, MacMullen C, Underwood P, Bhatia P, Steinkrauss L, Wanner L, Kaye R, Ruchelli E, Suchi M, Adzick NS (xaneiro de 2004). "Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation". The Journal of Clinical Endocrinology and Metabolism 89 (1): 288–96. PMID 14715863. doi:10.1210/jc.2003-030965.

jbc.org (Global: 4,455^th place; Galician: 611^th place)

Shashidharan P, Michaelidis TM, Robakis NK, Kresovali A, Papamatheakis J, Plaitakis A (xuño de 1994). "Novel human glutamate dehydrogenase expressed in neural and testicular tissues and encoded by an X-linked intronless gene". J. Biol. Chem. 269 (24): 16971–6. PMID 8207021. doi:10.1016/S0021-9258(19)89484-X. Arquivado dende o orixinal o 29 de setembro de 2007. Consultado o 01 de xaneiro de 2022.

nih.gov (Global: 4^th place; Galician: 6^th place)

ncbi.nlm.nih.gov

Shashidharan P, Michaelidis TM, Robakis NK, Kresovali A, Papamatheakis J, Plaitakis A (xuño de 1994). "Novel human glutamate dehydrogenase expressed in neural and testicular tissues and encoded by an X-linked intronless gene". J. Biol. Chem. 269 (24): 16971–6. PMID 8207021. doi:10.1016/S0021-9258(19)89484-X. Arquivado dende o orixinal o 29 de setembro de 2007. Consultado o 01 de xaneiro de 2022.
Smith TJ, Schmidt T, Fang J, Wu J, Siuzdak G, Stanley CA (maio de 2002). "The structure of apo human glutamate dehydrogenase details subunit communication and allostery". J. Mol. Biol. 318 (3): 765–77. PMID 12054821. doi:10.1016/S0022-2836(02)00161-4.
Banerjee S, Schmidt T, Fang J, Stanley CA, Smith TJ (abril de 2003). "Structural studies on ADP activation of mammalian glutamate dehydrogenase and the evolution of regulation". Biochemistry 42 (12): 3446–56. PMID 12653548. doi:10.1021/bi0206917.
Smith TJ, Peterson PE, Schmidt T, Fang J, Stanley CA (marzo de 2001). "Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation". J. Mol. Biol. 307 (2): 707–20. PMID 11254391. doi:10.1006/jmbi.2001.4499.
Peterson PE, Smith TJ (xullo de 1999). "The structure of bovine glutamate dehydrogenase provides insights into the mechanism of allostery". Structure 7 (7): 769–82. PMID 10425679. doi:10.1016/S0969-2126(99)80101-4.
George A, Bell JE (decembro de 1980). "Effects of adenosine 5'-diphosphate on bovine glutamate dehydrogenase: diethyl pyrocarbonate modification". Biochemistry 19 (26): 6057–61. PMID 7470450. doi:10.1021/bi00567a017.
Fang, J; Hsu, BY; MacMullen, CM; Poncz, M; Smith, TJ; Stanley, CA (2002). "Expression, purification and characterization of GLUD1 allosteric regulatory mutations". Biochem. J. 363 (Pt 1): 81–7. PMC 1222454. PMID 11903050. doi:10.1042/0264-6021:3630081.
Won JG, Tseng HS, Yang AH, Tang KT, Jap TS, Lee CH, Lin HD, Burcus N, Pittenger G, Vinik A (novembro de 2006). "Clinical features and morphological characterization of 10 patients with noninsulinoma pancreatogenous hypoglycaemia syndrome (NIPHS)". Clinical Endocrinology 65 (5): 566–78. PMID 17054456. doi:10.1111/j.1365-2265.2006.02629.x.
Pinney SE, MacMullen C, Becker S, Lin YW, Hanna C, Thornton P, Ganguly A, Shyng SL, Stanley CA (agosto de 2008). "Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations". The Journal of Clinical Investigation 118 (8): 2877–86. PMC 2441858. PMID 18596924. doi:10.1172/JCI35414.
"Entrez Gene: glutamate dehydrogenase 1".
Glaser B, Blech I, Krakinovsky Y, Ekstein J, Gillis D, Mazor-Aronovitch K, Landau H, Abeliovich D (outubro de 2011). "ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia". Genetics in Medicine 13 (10): 891–4. PMID 21716120. doi:10.1097/GIM.0b013e31821fea33.
Højlund K, Hansen T, Lajer M, Henriksen JE, Levin K, Lindholm J, Pedersen O, Beck-Nielsen H (xuño de 2004). "A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene". Diabetes 53 (6): 1592–8. PMID 15161766. doi:10.2337/diabetes.53.6.1592.
Mazor-Aronovitch K, Landau H, Gillis D (marzo de 2009). "Surgical versus non-surgical treatment of congenital hyperinsulinism". Pediatric Endocrinology Reviews 6 (3): 424–30. PMID 19396028.
Mazor-Aronovitch K, Gillis D, Lobel D, Hirsch HJ, Pinhas-Hamiel O, Modan-Moses D, Glaser B, Landau H (outubro de 2007). "Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism". European Journal of Endocrinology 157 (4): 491–7. PMID 17893264. doi:10.1530/EJE-07-0445.
Stanley CA, Thornton PS, Ganguly A, MacMullen C, Underwood P, Bhatia P, Steinkrauss L, Wanner L, Kaye R, Ruchelli E, Suchi M, Adzick NS (xaneiro de 2004). "Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation". The Journal of Clinical Endocrinology and Metabolism 89 (1): 288–96. PMID 14715863. doi:10.1210/jc.2003-030965.

web.archive.org (Global: 1^st place; Galician: 1^st place)

Shashidharan P, Michaelidis TM, Robakis NK, Kresovali A, Papamatheakis J, Plaitakis A (xuño de 1994). "Novel human glutamate dehydrogenase expressed in neural and testicular tissues and encoded by an X-linked intronless gene". J. Biol. Chem. 269 (24): 16971–6. PMID 8207021. doi:10.1016/S0021-9258(19)89484-X. Arquivado dende o orixinal o 29 de setembro de 2007. Consultado o 01 de xaneiro de 2022.

GLUD1 (Galician Wikipedia)

archive.org (Global: 6th place; Galician: 8th place)

doi.org (Global: 2nd place; Galician: 7th place)