|1.||Banks, Lawrence: 2 articles (10/2015 - 01/2013)|
|2.||Bergant, Martina: 2 articles (10/2015 - 01/2013)|
|3.||Wang, Xin: 2 articles (05/2015 - 04/2013)|
|4.||Hong, Wanjin: 2 articles (01/2014 - 04/2013)|
|5.||Loo, Li Shen: 2 articles (01/2014 - 04/2013)|
|6.||Jose, Pedro A: 2 articles (05/2013 - 01/2013)|
|7.||Villar, Van Anthony M: 2 articles (05/2013 - 01/2013)|
|8.||Lee, Hewang: 2 articles (05/2013 - 01/2013)|
|9.||Yang, Yu: 2 articles (05/2013 - 01/2013)|
|10.||Armando, Ines: 2 articles (05/2013 - 01/2013)|
12/01/2014 - "Sorting nexin 10 (SNX10), the unique member of the SNX family having vacuolation activity in cells, was shown to be involved in the development of autosomal recessive osteopetrosis (ARO) in recent genetic studies. "
03/01/2015 - "Mutations in sorting nexin 10 (Snx10) have recently been found to account for roughly 4% of all human malignant osteopetrosis, some of them fatal. "
01/01/2013 - "Recently a mutation in the SNX10 gene that belongs to the sorting nexin family was identified as a cause of a new subset of human autosomal recessive osteopetrosis. "
01/01/2013 - "Previous studies have shown that the human papillomavirus type 16 (HPV-16) L2 capsid protein plays an essential role in viral infection, in part through its interaction with sorting nexin 17 (SNX17). "
10/01/2015 - "We show that small interfering RNA (siRNA)-mediated knockdown of SNX27 alone leads to a marginal reduction in the efficiency of viral infection but that double knockdown of both sorting nexins results in a striking reduction in infection, greater than that observed for the knockdown of either sorting nexin alone. "
|3.||Temporal Lobe Epilepsy
|4.||Colorectal Neoplasms (Colorectal Cancer)
01/01/2007 - "A disruption of sorting nexin 3 (SNX3) on 6q21 was previously reported in a patient with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and t(6;13)(q21;q12) but no SNX3 mutations were identified in another sporadic case of MMEP, suggesting involvement of another gene. "
12/01/2002 - "Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype."
|1.||Capsid Proteins (Capsid Protein)
|4.||Carrier Proteins (Binding Protein)
|5.||Small Interfering RNA (siRNA)
|6.||Glutamate Receptors (Glutamate Receptor)
|7.||Dopamine Receptors (Dopamine Receptor)
|8.||Proteins (Proteins, Gene)
|10.||mono(2-methacryloyloxy)ethyl phthalate (MMEP)