GRIN2A (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "GRIN2A" in Persian language version.

refsWebsite

Global rank Persian rank

16nih.gov

4^th place

5^th place

13doi.org

2^nd place

5worldcat.org

5^th place

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1ensembl.org

1,626^th place

1,252^nd place

1harvard.edu

18^th place

50^th place

1semanticscholar.org

11^th place

52^nd place

1science.org

1,160^th place

4,431^st place

1wiley.com

222^nd place

185^th place

1elsevier.com

610^th place

762^nd place

doi.org

Kalsi G, Whiting P, Bourdelles BL, Callen D, Barnard EA, Gurling H (February 1998). "Localization of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels". Genomics. 47 (3): 423–425. doi:10.1006/geno.1997.5132. PMID 9480759.
Warming H, Pegasiou CM, Pitera AP, Kariis H, Houghton SD, Kurbatskaya K, et al. (July 2019). "A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain". Molecular Brain. 12 (1): 64. doi:10.1186/s13041-019-0485-9. PMC 6610962. PMID 31272478.
Herbrechter R, Hube N, Buchholz R, Reiner A (July 2021). "Splicing and editing of ionotropic glutamate receptors: a comprehensive analysis based on human RNA-Seq data". Cellular and Molecular Life Sciences. 78 (14): 5605–5630. doi:10.1007/s00018-021-03865-z. PMC 8257547. PMID 34100982.
Hamza TH, Chen H, Hill-Burns EM, Rhodes SL, Montimurro J, Kay DM, et al. (August 2011). "Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee". PLOS Genetics. 7 (8): e1002237. doi:10.1371/journal.pgen.1002237. PMC 3158052. PMID 21876681.
Yamada-Fowler N, Fredrikson M, Söderkvist P (June 2014). "Caffeine interaction with glutamate receptor gene GRIN2A: Parkinson's disease in Swedish population". PLOS ONE. 9 (6): e99294. Bibcode:2014PLoSO...999294Y. doi:10.1371/journal.pone.0099294. PMC 4051678. PMID 24915238.
Venkateswaran S, Myers KA, Smith AC, Beaulieu CL, Schwartzentruber JA, Majewski J, et al. (July 2014). "Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation". Epilepsia. 55 (7): e75–e79. doi:10.1111/epi.12663. PMID 24903190. S2CID 205116246.
Yuan H, Low CM, Moody OA, Jenkins A, Traynelis SF (July 2015). "Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases". Molecular Pharmacology. 88 (1): 203–217. doi:10.1124/mol.115.097998. PMC 4468639. PMID 25904555.
Gardoni, Fabrizio; Mauceri, Daniela; Fiorentini, Chiara; Bellone, Camilla; Missale, Cristina; Cattabeni, Flaminio; Luca, Monica Di (2003). "CaMKII-dependent Phosphorylation Regulates SAP97/NR2A Interaction". Journal of Biological Chemistry. 278 (45): 44745–44752. doi:10.1074/jbc.m303576200. ISSN 0021-9258.
Irie, M.; Hata, Y.; Takeuchi, M.; Ichtchenko, K.; Toyoda, A.; Hirao, K.; Takai, Y.; Rosahl, T. W.; Südhof, T. C. (1997-09-05). "Binding of Neuroligins to PSD-95". Science (به انگلیسی). 277 (5331): 1511–1515. doi:10.1126/science.277.5331.1511. ISSN 0036-8075.
Lim, Indra Adi; Hall, Duane D.; Hell, Johannes W. (2006). "Selectivity and Promiscuity of the First and Second PDZ Domains of PSD-95 and Synapse-associated Protein 102". Journal of Biological Chemistry. 277 (24): 21697–21711. doi:10.1074/jbc.m112339200. ISSN 0021-9258.
Hou, Xiao-Yu; Zhang, Guang-Yi; Yan, Jing-Zhi; Chen, Min; Liu, Yong (2002). "Activation of NMDA receptors and L-type voltage-gated calcium channels mediates enhanced formation of Fyn–PSD95–NR2A complex after transient brain ischemia". Brain Research. 955 (1–2): 123–132. doi:10.1016/s0006-8993(02)03376-0. ISSN 0006-8993.
Satoh, Kiyotoshi; Yanai, Hiroyuki; Senda, Takao; Kohu, Kazuyoshi; Nakamura, Tsutomu; Okumura, Nobuaki; Matsumine, Akihiko; Kobayashi, Shigeru; Toyoshima, Kumao (1997). "DAP‐1, a novel protein that interacts with the guanylate kinase‐like domains of hDLG and PSD‐95". Genes to Cells (به انگلیسی). 2 (6): 415–424. doi:10.1046/j.1365-2443.1997.1310329.x. ISSN 1356-9597.
Hou, Xiao-Yu; Zhang, Guang-Yi; Yan, Jing-Zhi; Chen, Min; Liu, Yong (2002). "Activation of NMDA receptors and L-type voltage-gated calcium channels mediates enhanced formation of Fyn–PSD95–NR2A complex after transient brain ischemia". Brain Research (به انگلیسی). 955 (1–2): 123–132. doi:10.1016/S0006-8993(02)03376-0.

elsevier.com

linkinghub.elsevier.com

Hou, Xiao-Yu; Zhang, Guang-Yi; Yan, Jing-Zhi; Chen, Min; Liu, Yong (2002). "Activation of NMDA receptors and L-type voltage-gated calcium channels mediates enhanced formation of Fyn–PSD95–NR2A complex after transient brain ischemia". Brain Research (به انگلیسی). 955 (1–2): 123–132. doi:10.1016/S0006-8993(02)03376-0.

ensembl.org

May2017.archive.ensembl.org

GRCm38: Ensembl release 89: ENSMUSG00000059003 - Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Yamada-Fowler N, Fredrikson M, Söderkvist P (June 2014). "Caffeine interaction with glutamate receptor gene GRIN2A: Parkinson's disease in Swedish population". PLOS ONE. 9 (6): e99294. Bibcode:2014PLoSO...999294Y. doi:10.1371/journal.pone.0099294. PMC 4051678. PMID 24915238.

nih.gov

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Warming H, Pegasiou CM, Pitera AP, Kariis H, Houghton SD, Kurbatskaya K, et al. (July 2019). "A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain". Molecular Brain. 12 (1): 64. doi:10.1186/s13041-019-0485-9. PMC 6610962. PMID 31272478.
Herbrechter R, Hube N, Buchholz R, Reiner A (July 2021). "Splicing and editing of ionotropic glutamate receptors: a comprehensive analysis based on human RNA-Seq data". Cellular and Molecular Life Sciences. 78 (14): 5605–5630. doi:10.1007/s00018-021-03865-z. PMC 8257547. PMID 34100982.
"Entrez Gene: GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A".
Hamza TH, Chen H, Hill-Burns EM, Rhodes SL, Montimurro J, Kay DM, et al. (August 2011). "Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee". PLOS Genetics. 7 (8): e1002237. doi:10.1371/journal.pgen.1002237. PMC 3158052. PMID 21876681.
Yamada-Fowler N, Fredrikson M, Söderkvist P (June 2014). "Caffeine interaction with glutamate receptor gene GRIN2A: Parkinson's disease in Swedish population". PLOS ONE. 9 (6): e99294. Bibcode:2014PLoSO...999294Y. doi:10.1371/journal.pone.0099294. PMC 4051678. PMID 24915238.
Yuan H, Low CM, Moody OA, Jenkins A, Traynelis SF (July 2015). "Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases". Molecular Pharmacology. 88 (1): 203–217. doi:10.1124/mol.115.097998. PMC 4468639. PMID 25904555.
""A developmental change in NMDA receptor-associated proteins at hippocampal synapses"" (به انگلیسی).

pubmed.ncbi.nlm.nih.gov

Kalsi G, Whiting P, Bourdelles BL, Callen D, Barnard EA, Gurling H (February 1998). "Localization of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels". Genomics. 47 (3): 423–425. doi:10.1006/geno.1997.5132. PMID 9480759.
Warming H, Pegasiou CM, Pitera AP, Kariis H, Houghton SD, Kurbatskaya K, et al. (July 2019). "A primate-specific short GluN2A-NMDA receptor isoform is expressed in the human brain". Molecular Brain. 12 (1): 64. doi:10.1186/s13041-019-0485-9. PMC 6610962. PMID 31272478.
Herbrechter R, Hube N, Buchholz R, Reiner A (July 2021). "Splicing and editing of ionotropic glutamate receptors: a comprehensive analysis based on human RNA-Seq data". Cellular and Molecular Life Sciences. 78 (14): 5605–5630. doi:10.1007/s00018-021-03865-z. PMC 8257547. PMID 34100982.
Hamza TH, Chen H, Hill-Burns EM, Rhodes SL, Montimurro J, Kay DM, et al. (August 2011). "Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee". PLOS Genetics. 7 (8): e1002237. doi:10.1371/journal.pgen.1002237. PMC 3158052. PMID 21876681.
Yamada-Fowler N, Fredrikson M, Söderkvist P (June 2014). "Caffeine interaction with glutamate receptor gene GRIN2A: Parkinson's disease in Swedish population". PLOS ONE. 9 (6): e99294. Bibcode:2014PLoSO...999294Y. doi:10.1371/journal.pone.0099294. PMC 4051678. PMID 24915238.
Venkateswaran S, Myers KA, Smith AC, Beaulieu CL, Schwartzentruber JA, Majewski J, et al. (July 2014). "Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation". Epilepsia. 55 (7): e75–e79. doi:10.1111/epi.12663. PMID 24903190. S2CID 205116246.
Yuan H, Low CM, Moody OA, Jenkins A, Traynelis SF (July 2015). "Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases". Molecular Pharmacology. 88 (1): 203–217. doi:10.1124/mol.115.097998. PMC 4468639. PMID 25904555.

science.org

Irie, M.; Hata, Y.; Takeuchi, M.; Ichtchenko, K.; Toyoda, A.; Hirao, K.; Takai, Y.; Rosahl, T. W.; Südhof, T. C. (1997-09-05). "Binding of Neuroligins to PSD-95". Science (به انگلیسی). 277 (5331): 1511–1515. doi:10.1126/science.277.5331.1511. ISSN 0036-8075.

semanticscholar.org

api.semanticscholar.org

Venkateswaran S, Myers KA, Smith AC, Beaulieu CL, Schwartzentruber JA, Majewski J, et al. (July 2014). "Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation". Epilepsia. 55 (7): e75–e79. doi:10.1111/epi.12663. PMID 24903190. S2CID 205116246.

wiley.com

onlinelibrary.wiley.com

Satoh, Kiyotoshi; Yanai, Hiroyuki; Senda, Takao; Kohu, Kazuyoshi; Nakamura, Tsutomu; Okumura, Nobuaki; Matsumine, Akihiko; Kobayashi, Shigeru; Toyoshima, Kumao (1997). "DAP‐1, a novel protein that interacts with the guanylate kinase‐like domains of hDLG and PSD‐95". Genes to Cells (به انگلیسی). 2 (6): 415–424. doi:10.1046/j.1365-2443.1997.1310329.x. ISSN 1356-9597.

worldcat.org

Gardoni, Fabrizio; Mauceri, Daniela; Fiorentini, Chiara; Bellone, Camilla; Missale, Cristina; Cattabeni, Flaminio; Luca, Monica Di (2003). "CaMKII-dependent Phosphorylation Regulates SAP97/NR2A Interaction". Journal of Biological Chemistry. 278 (45): 44745–44752. doi:10.1074/jbc.m303576200. ISSN 0021-9258.
Irie, M.; Hata, Y.; Takeuchi, M.; Ichtchenko, K.; Toyoda, A.; Hirao, K.; Takai, Y.; Rosahl, T. W.; Südhof, T. C. (1997-09-05). "Binding of Neuroligins to PSD-95". Science (به انگلیسی). 277 (5331): 1511–1515. doi:10.1126/science.277.5331.1511. ISSN 0036-8075.
Lim, Indra Adi; Hall, Duane D.; Hell, Johannes W. (2006). "Selectivity and Promiscuity of the First and Second PDZ Domains of PSD-95 and Synapse-associated Protein 102". Journal of Biological Chemistry. 277 (24): 21697–21711. doi:10.1074/jbc.m112339200. ISSN 0021-9258.
Hou, Xiao-Yu; Zhang, Guang-Yi; Yan, Jing-Zhi; Chen, Min; Liu, Yong (2002). "Activation of NMDA receptors and L-type voltage-gated calcium channels mediates enhanced formation of Fyn–PSD95–NR2A complex after transient brain ischemia". Brain Research. 955 (1–2): 123–132. doi:10.1016/s0006-8993(02)03376-0. ISSN 0006-8993.
Satoh, Kiyotoshi; Yanai, Hiroyuki; Senda, Takao; Kohu, Kazuyoshi; Nakamura, Tsutomu; Okumura, Nobuaki; Matsumine, Akihiko; Kobayashi, Shigeru; Toyoshima, Kumao (1997). "DAP‐1, a novel protein that interacts with the guanylate kinase‐like domains of hDLG and PSD‐95". Genes to Cells (به انگلیسی). 2 (6): 415–424. doi:10.1046/j.1365-2443.1997.1310329.x. ISSN 1356-9597.