Mus musculus survival motor neuron 1 (Smn1), transcript variant 2, mRN - Nucleotide

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Systemic LPS Administration Stimulates the Activation of Non-Neuronal Cells in an Experimental Model of Spinal Muscular Atrophy. [Cells. 2024]
Systemic LPS Administration Stimulates the Activation of Non-Neuronal Cells in an Experimental Model of Spinal Muscular Atrophy.
Karafoulidou E, Kesidou E, Theotokis P, Konstantinou C, Nella MK, Michailidou I, Touloumi O, Polyzoidou E, Salamotas I, Einstein O, et al. Cells. 2024 May 4; 13(9). Epub 2024 May 4.
Improved gene therapy for spinal muscular atrophy in mice using codon-optimized hSMN1 transgene and hSMN1 gene-derived promotor. [EMBO Mol Med. 2024]
Improved gene therapy for spinal muscular atrophy in mice using codon-optimized hSMN1 transgene and hSMN1 gene-derived promotor.
Xie Q, Chen X, Ma H, Zhu Y, Ma Y, Jalinous L, Cox GF, Weaver F, Yang J, Kennedy Z, et al. EMBO Mol Med. 2024 Apr; 16(4):945-965. Epub 2024 Feb 27.
Depletion of SMN protein in mesenchymal progenitors impairs the development of bone and neuromuscular junction in spinal muscular atrophy. [Elife. 2024]
Depletion of SMN protein in mesenchymal progenitors impairs the development of bone and neuromuscular junction in spinal muscular atrophy.
Hann SH, Kim SY, Kim YL, Jo YW, Kang JS, Park H, Choi SY, Kong YY. Elife. 2024 Feb 6; 12. Epub 2024 Feb 6.

RefSeq protein product
See the reference protein sequence for survival motor neuron protein isoform 2 (NP_001239558.1).

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Nucleotide