CUL7 (Portuguese Wikipedia)
Analysis of information sources in references of the Wikipedia article "CUL7" in Portuguese language version.
refsWebsite
Global rank
Portuguese rank
43rd place
440th place
234th place
190th place
doi.org (Global: 2nd place; Portuguese: 4th place)
dx.doi.org
- Dias DC, Dolios G, Wang R, Pan ZQ (dezembro de 2002). «CUL7: A DOC domain-containing cullin selectively binds Skp1.Fbx29 to form an SCF-like complex». Proc Natl Acad Sci U S A. 99 (26): 16601–6. PMC 139190
. PMID 12481031. doi:10.1073/pnas.252646399 - Arai T, Kasper JS, Skaar JR, Ali SH, Takahashi C, DeCaprio JA (agosto de 2003). «Targeted disruption of p185/Cul7 gene results in abnormal vascular morphogenesis». Proc Natl Acad Sci U S A. 100 (17): 9855–60. PMC 187864. PMID 12904573. doi:10.1073/pnas.1733908100
- Erickson, Robert P; Wynshaw-Boris, Anthony Joseph (2016). Epstein's Inborn Errors of Development: The Molecular Basis of Clinical Disorders of Morphogenesis: 3M Syndrome. Oxford Medicine Online. 3e.d. [S.l.: s.n.] ISBN 9780199934522. doi:10.1093/med/9780199934522.001.0001
- Holder-Espinasse, Valérie; Irving, Melita; Cormier-Daire (2 de março de 2011). «Clinical utility gene card for: 3M syndrome». European Journal of Human Genetics. 19 (9). 1017 páginas. PMC 3179355. PMID 21364696. doi:10.1038/ejhg.2011.32
nature.com (Global: 234th place; Portuguese: 190th place)
- Holder-Espinasse, Valérie; Irving, Melita; Cormier-Daire (2 de março de 2011). «Clinical utility gene card for: 3M syndrome». European Journal of Human Genetics. 19 (9). 1017 páginas. PMC 3179355. PMID 21364696. doi:10.1038/ejhg.2011.32
nih.gov (Global: 4th place; Portuguese: 8th place)
ncbi.nlm.nih.gov
- «Human PubMed Reference:»
- Dias DC, Dolios G, Wang R, Pan ZQ (dezembro de 2002). «CUL7: A DOC domain-containing cullin selectively binds Skp1.Fbx29 to form an SCF-like complex». Proc Natl Acad Sci U S A. 99 (26): 16601–6. PMC 139190. PMID 12481031. doi:10.1073/pnas.252646399
- Arai T, Kasper JS, Skaar JR, Ali SH, Takahashi C, DeCaprio JA (agosto de 2003). «Targeted disruption of p185/Cul7 gene results in abnormal vascular morphogenesis». Proc Natl Acad Sci U S A. 100 (17): 9855–60. PMC 187864. PMID 12904573. doi:10.1073/pnas.1733908100
- «Entrez Gene: CUL7 cullin 7»
- Holder-Espinasse, Valérie; Irving, Melita; Cormier-Daire (2 de março de 2011). «Clinical utility gene card for: 3M syndrome». European Journal of Human Genetics. 19 (9). 1017 páginas. PMC 3179355. PMID 21364696. doi:10.1038/ejhg.2011.32
ghr.nlm.nih.gov
- «3-M syndrome». Genetics Home Reference (GHR). 12 de dezembro de 2017