NEK8 (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "NEK8" in Arabic language version.

refsWebsite
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4th place
6th place
2nd place
5th place
1st place
1st place

doi.org (Global: 2nd place; Arabic: 5th place)

  • Otto EA، Trapp ML، Schultheiss UT، Helou J، Quarmby LM، Hildebrandt F (مارس 2008). "NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis". J. Am. Soc. Nephrol. ج. 19 ع. 3: 587–92. DOI:10.1681/ASN.2007040490. PMC:2391043. PMID:18199800.
  • Lancaster MA، Gleeson JG (يونيو 2009). "The primary cilium as a cellular signaling center: lessons from disease". Curr. Opin. Genet. Dev. ج. 19 ع. 3: 220–9. DOI:10.1016/j.gde.2009.04.008. PMC:2953615. PMID:19477114.
  • Zalli، D.؛ Bayliss, R.؛ Fry, A. M. (21 نوفمبر 2011). "The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis". Human Molecular Genetics. ج. 21 ع. 5: 1155–1171. DOI:10.1093/hmg/ddr544. PMC:3277313. PMID:22106379.

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

ncbi.nlm.nih.gov

  • Otto EA، Trapp ML، Schultheiss UT، Helou J، Quarmby LM، Hildebrandt F (مارس 2008). "NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis". J. Am. Soc. Nephrol. ج. 19 ع. 3: 587–92. DOI:10.1681/ASN.2007040490. PMC:2391043. PMID:18199800.
  • "Entrez Gene: NIMA (never in mitosis gene a)- related kinase 8". مؤرشف من الأصل في 2010-03-08.
  • "NEK8 NIMA related kinase 8 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. مؤرشف من الأصل في 2010-03-08. اطلع عليه بتاريخ 2025-03-26.
  • Lancaster MA، Gleeson JG (يونيو 2009). "The primary cilium as a cellular signaling center: lessons from disease". Curr. Opin. Genet. Dev. ج. 19 ع. 3: 220–9. DOI:10.1016/j.gde.2009.04.008. PMC:2953615. PMID:19477114.
  • Zalli، D.؛ Bayliss, R.؛ Fry, A. M. (21 نوفمبر 2011). "The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis". Human Molecular Genetics. ج. 21 ع. 5: 1155–1171. DOI:10.1093/hmg/ddr544. PMC:3277313. PMID:22106379.

pubmed.ncbi.nlm.nih.gov

  • Otto EA، Trapp ML، Schultheiss UT، Helou J، Quarmby LM، Hildebrandt F (مارس 2008). "NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis". J. Am. Soc. Nephrol. ج. 19 ع. 3: 587–92. DOI:10.1681/ASN.2007040490. PMC:2391043. PMID:18199800.
  • Lancaster MA، Gleeson JG (يونيو 2009). "The primary cilium as a cellular signaling center: lessons from disease". Curr. Opin. Genet. Dev. ج. 19 ع. 3: 220–9. DOI:10.1016/j.gde.2009.04.008. PMC:2953615. PMID:19477114.
  • Zalli، D.؛ Bayliss, R.؛ Fry, A. M. (21 نوفمبر 2011). "The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis". Human Molecular Genetics. ج. 21 ع. 5: 1155–1171. DOI:10.1093/hmg/ddr544. PMC:3277313. PMID:22106379.

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