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Showing results 1-7 of 7

2020
1 Katoozi, Shirin; Shreyas, Rao; Skauli, Nadia; Froehner, Stanley C.; Ottersen, Ole Petter; Adams, Marv; Amiry-Moghaddam, Mahmood.
Functional specialization of retinal Müller cell endfeet depends on an interplay between two syntrophin isoforms. Molecular Brain 2020 ;Volume 13.
UiO Untitled
 
2 Katoozi, Shirin; Skauli, Nadia; Rahmani, Soulmaz; Deshpande, Tushar; Ezan, Pascal; Palazzo, Claudia; Steinhäuser, Christian; Frigeri, Antonio; Cohen-Salmon, Martine; Ottersen, Ole Petter; Amiry-Moghaddam, Mahmood.
Uncoupling of the Astrocyte Syncytium Differentially Affects AQP4 Isoforms. Cells 2020
UiO Untitled
 
3 Prydz, Agnete; Stahl, Katja; Rahmani, Soulmaz; Skauli, Nadia; Skare, Øivind; Ottersen, Ole Petter; Amiry-Moghaddam, Mahmood.
Pro-inflammatory role of AQP4 in mice subjected to intrastriatal injections of the Parkinsonogenic toxin MPP. Cells 2020 ;Volume 9:2418.(11) p. -
STAMI UiO Untitled
 
2019
4 Rao, Shreyas Balachandra; Katoozi, Shirin; Skauli, Nadia; Froehner, Stanley C.; Ottersen, Ole Petter; Adams, Marvin E.; Amiry-Moghaddam, Mahmood.
Targeted deletion of β1-syntrophin causes a loss of Kir 4.1 from Müller cell endfeet in mouse retina. Glia 2019 ;Volume 67.(6) p. 1138-1149
UiO Untitled
 
2018
5 Stahl, Katja; Rahmani, Soulmaz; Prydz, Agnete; Skauli, Nadia; MacAulay, Nanna; Mylonakou, Maria-Niki; Torp, Reidun; Skare, Øivind; Berg, Torill; Leergaard, Trygve Brauns; Paulsen, Ragnhild Elisabeth; Ottersen, Ole Petter; Amiry-Moghaddam, Mahmood.
Targeted deletion of the aquaglyceroporin AQP9 is protective in a mouse model of Parkinson's disease. PLOS ONE 2018 ;Volume 13.(3)
STAMI UiO Untitled
 
2017
6 Katoozi, Shirin; Skauli, Nadia; Rahmani, Soulmaz; Camassa, Laura Maria Azzurra; Boldt, Henning Bunsow; Ottersen, Ole Petter; Amiry-Moghaddam, Mahmood.
Targeted deletion of Aqp4 promotes the formation of astrocytic gap junctions. Brain Structure and Function 2017 p. 1-14
UiO Untitled
 
2016
7 Skauli, Nadia; Wallace, Sean Ciaran; Chiang, Samuel C.C.; Barøy, Tuva; Holmgren, Asbjørn; Stray-Pedersen, Asbjørg; Bryceson, Yenan T.; Strømme, Petter; Frengen, Eirik; Misceo, Doriana.
Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype. Genes 2016 ;Volume 7.(12) p. -
OUS UiO Untitled