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Hypertryptophanemia (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hypertryptophanemia" in English language version.

refsWebsite
Global rank English rank
14nih.gov
4th place
4th place
13doi.org
2nd place
2nd place
6worldcat.org
5th place
5th place
5semanticscholar.org
11th place
8th place
2omim.org
4,380th place
4,305th place
1nutrition.org
7,878th place
low place
1zenodo.org
621st place
380th place

doi.org

  • Martin JR, Mellor CS, Fraser FC (April 1995). "Familial hypertryptophanemia in two siblings". Clin. Genet. 47 (4): 180–183. doi:10.1111/j.1399-0004.1995.tb03956.x. PMID 7628119. S2CID 27203561.
  • Snedden W, Mellor CS, Martin JR (July 1983). "Familial hypertryptophanemia, tryptophanuria and indoleketonuria". Clinica Chimica Acta. 131 (3): 247–256. doi:10.1016/0009-8981(83)90094-3. ISSN 0009-8981. PMID 6883719.
  • Snedden W, Mellor CS, Martin JR (November 1982). "Hypertryptophanemia and indoleketonuria in two mentally subnormal siblings" (Free full text). The New England Journal of Medicine. 307 (22): 1405. doi:10.1056/NEJM198211253072219. ISSN 0028-4793. PMID 7133092.
  • Seow HF, Bröer S, Bröer A, Bailey CG, Potter SJ, Cavanaugh JA, Rasko JE (September 2004). "Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19". Nature Genetics. 36 (9): 1003–1007. doi:10.1038/ng1406. PMID 15286788.
  • Dunn MF, Niks D, Ngo H, Barends TR, Schlichting I (June 2008). "Tryptophan synthase: the workings of a channeling nanomachine". Trends in Biochemical Sciences. 33 (6): 254–264. doi:10.1016/j.tibs.2008.04.008. PMID 18486479.
  • Houben KF, Dunn MF (March 1990). "Allosteric effects acting over a distance of 20-25 A in the Escherichia coli tryptophan synthase bienzyme complex increase ligand affinity and cause redistribution of covalent intermediates". Biochemistry. 29 (9): 2421–2429. doi:10.1021/bi00461a028. ISSN 0006-2960. PMID 2186812.
  • Reeds PJ (1 July 2000). "Dispensable and indispensable amino acids for humans" (Free full text). The Journal of Nutrition. 130 (7): 1835S – 1840S. doi:10.1093/jn/130.7.1835S. ISSN 0022-3166. PMID 10867060.
  • Stone TW (January 2001). "Endogenous neurotoxins from tryptophan". Toxicon. 39 (1): 61–73. doi:10.1016/S0041-0101(00)00156-2. ISSN 0041-0101. PMID 10936623.
  • Stone TW, Mackay GM, Forrest CM, Clark CJ, Darlington LG (July 2003). "Tryptophan metabolites and brain disorders". Clinical Chemistry and Laboratory Medicine. 41 (7): 852–859. doi:10.1515/CCLM.2003.129. PMID 12940508. S2CID 21169913.
  • Stone TW, Forrest CM, Mackay GM, Stoy N, Darlington LG (December 2007). "Tryptophan, adenosine, neurodegeneration and neuroprotection". Metabolic Brain Disease. 22 (3–4): 337–352. doi:10.1007/s11011-007-9064-3. PMID 17712616. S2CID 5823156.
  • Stone TW (April 2001). "Kynurenic acid antagonists and kynurenine pathway inhibitors". Expert Opin Investig Drugs. 10 (4): 633–645. doi:10.1517/13543784.10.4.633. PMID 11281814. S2CID 30077788.
  • Ruddick JP, Evans AK, Nutt DJ, Lightman SL, Rook GA, Lowry CA (August 2006). "Tryptophan metabolism in the central nervous system: medical implications". Expert Reviews in Molecular Medicine. 8 (20): 1–27. doi:10.1017/S1462399406000068. PMID 16942634. S2CID 36859939.
  • Moroni F (June 1999). "Tryptophan metabolism and brain function: focus on kynurenine and other indole metabolites". European Journal of Pharmacology. 375 (1–3): 87–100. doi:10.1016/S0014-2999(99)00196-X. ISSN 0014-2999. PMID 10443567.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Martin JR, Mellor CS, Fraser FC (April 1995). "Familial hypertryptophanemia in two siblings". Clin. Genet. 47 (4): 180–183. doi:10.1111/j.1399-0004.1995.tb03956.x. PMID 7628119. S2CID 27203561.
  • Snedden W, Mellor CS, Martin JR (July 1983). "Familial hypertryptophanemia, tryptophanuria and indoleketonuria". Clinica Chimica Acta. 131 (3): 247–256. doi:10.1016/0009-8981(83)90094-3. ISSN 0009-8981. PMID 6883719.
  • Snedden W, Mellor CS, Martin JR (November 1982). "Hypertryptophanemia and indoleketonuria in two mentally subnormal siblings" (Free full text). The New England Journal of Medicine. 307 (22): 1405. doi:10.1056/NEJM198211253072219. ISSN 0028-4793. PMID 7133092.
  • Seow HF, Bröer S, Bröer A, Bailey CG, Potter SJ, Cavanaugh JA, Rasko JE (September 2004). "Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19". Nature Genetics. 36 (9): 1003–1007. doi:10.1038/ng1406. PMID 15286788.
  • Dunn MF, Niks D, Ngo H, Barends TR, Schlichting I (June 2008). "Tryptophan synthase: the workings of a channeling nanomachine". Trends in Biochemical Sciences. 33 (6): 254–264. doi:10.1016/j.tibs.2008.04.008. PMID 18486479.
  • Houben KF, Dunn MF (March 1990). "Allosteric effects acting over a distance of 20-25 A in the Escherichia coli tryptophan synthase bienzyme complex increase ligand affinity and cause redistribution of covalent intermediates". Biochemistry. 29 (9): 2421–2429. doi:10.1021/bi00461a028. ISSN 0006-2960. PMID 2186812.
  • Reeds PJ (1 July 2000). "Dispensable and indispensable amino acids for humans" (Free full text). The Journal of Nutrition. 130 (7): 1835S – 1840S. doi:10.1093/jn/130.7.1835S. ISSN 0022-3166. PMID 10867060.
  • Stone TW (January 2001). "Endogenous neurotoxins from tryptophan". Toxicon. 39 (1): 61–73. doi:10.1016/S0041-0101(00)00156-2. ISSN 0041-0101. PMID 10936623.
  • Stone TW, Mackay GM, Forrest CM, Clark CJ, Darlington LG (July 2003). "Tryptophan metabolites and brain disorders". Clinical Chemistry and Laboratory Medicine. 41 (7): 852–859. doi:10.1515/CCLM.2003.129. PMID 12940508. S2CID 21169913.
  • Stone TW, Forrest CM, Mackay GM, Stoy N, Darlington LG (December 2007). "Tryptophan, adenosine, neurodegeneration and neuroprotection". Metabolic Brain Disease. 22 (3–4): 337–352. doi:10.1007/s11011-007-9064-3. PMID 17712616. S2CID 5823156.
  • Stone TW (April 2001). "Kynurenic acid antagonists and kynurenine pathway inhibitors". Expert Opin Investig Drugs. 10 (4): 633–645. doi:10.1517/13543784.10.4.633. PMID 11281814. S2CID 30077788.
  • Ruddick JP, Evans AK, Nutt DJ, Lightman SL, Rook GA, Lowry CA (August 2006). "Tryptophan metabolism in the central nervous system: medical implications". Expert Reviews in Molecular Medicine. 8 (20): 1–27. doi:10.1017/S1462399406000068. PMID 16942634. S2CID 36859939.
  • Moroni F (June 1999). "Tryptophan metabolism and brain function: focus on kynurenine and other indole metabolites". European Journal of Pharmacology. 375 (1–3): 87–100. doi:10.1016/S0014-2999(99)00196-X. ISSN 0014-2999. PMID 10443567.

toxnet.nlm.nih.gov

nutrition.org

jn.nutrition.org

omim.org

semanticscholar.org

api.semanticscholar.org

  • Martin JR, Mellor CS, Fraser FC (April 1995). "Familial hypertryptophanemia in two siblings". Clin. Genet. 47 (4): 180–183. doi:10.1111/j.1399-0004.1995.tb03956.x. PMID 7628119. S2CID 27203561.
  • Stone TW, Mackay GM, Forrest CM, Clark CJ, Darlington LG (July 2003). "Tryptophan metabolites and brain disorders". Clinical Chemistry and Laboratory Medicine. 41 (7): 852–859. doi:10.1515/CCLM.2003.129. PMID 12940508. S2CID 21169913.
  • Stone TW, Forrest CM, Mackay GM, Stoy N, Darlington LG (December 2007). "Tryptophan, adenosine, neurodegeneration and neuroprotection". Metabolic Brain Disease. 22 (3–4): 337–352. doi:10.1007/s11011-007-9064-3. PMID 17712616. S2CID 5823156.
  • Stone TW (April 2001). "Kynurenic acid antagonists and kynurenine pathway inhibitors". Expert Opin Investig Drugs. 10 (4): 633–645. doi:10.1517/13543784.10.4.633. PMID 11281814. S2CID 30077788.
  • Ruddick JP, Evans AK, Nutt DJ, Lightman SL, Rook GA, Lowry CA (August 2006). "Tryptophan metabolism in the central nervous system: medical implications". Expert Reviews in Molecular Medicine. 8 (20): 1–27. doi:10.1017/S1462399406000068. PMID 16942634. S2CID 36859939.

worldcat.org

search.worldcat.org

zenodo.org