Homo sapiens SLITL1 gene

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SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice. [Nat Commun. 2022]
SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.
El Chehadeh S, Han KA, Kim D, Jang G, Bakhtiari S, Lim D, Kim HY, Kim J, Kim H, Wynn J, et al. Nat Commun. 2022 Jul 15; 13(1):4112. Epub 2022 Jul 15.
Slitrk2 deficiency causes hyperactivity with altered vestibular function and serotonergic dysregulation. [iScience. 2022]
Slitrk2 deficiency causes hyperactivity with altered vestibular function and serotonergic dysregulation.
Katayama KI, Morimura N, Kobayashi K, Corbett D, Okamoto T, Ornthanalai VG, Matsunaga H, Fujita W, Matsumoto Y, Akagi T, et al. iScience. 2022 Jul 15; 25(7):104604. Epub 2022 Jun 14.
The Functional Proximal Proteome of Oncogenic Ras Includes mTORC2. [Mol Cell. 2019]
The Functional Proximal Proteome of Oncogenic Ras Includes mTORC2.
Kovalski JR, Bhaduri A, Zehnder AM, Neela PH, Che Y, Wozniak GG, Khavari PA. Mol Cell. 2019 Feb 21; 73(4):830-844.e12. Epub 2019 Jan 10.