Figure S3. Pacer mRNA levels in the lumbar spinal cord from sALS patients and fALS mouse models. a, Human Pacer (hPacer) and b, human Rubicon (hRubicon) mRNA expression was determined by qPCR in postmortem spinal cord sections from sALS patients and age-matched control subjects. Left panel, cervical spinal cord section with Controls n=2 and sALS patients n=6; middle panel, thoracic spinal cord section with Controls n=2 and sALS patients n=7; and right panel, lumbar spinal cord section with Controls n=6 and sALS patients n=7. β-Actin mRNA levels were used for normalization. c, Pacer and Rubicon mRNA expression was determined by qPCR in lumbar spinal cord samples of late symptomatic TDP43A315T transgenic mice (TDP43A315T-Tg, n=5) and their no...
Figure S1. APA Heat map for the ten genes that undergo shortening of their 3’UTRs and ten genes that...
Figure S4. Immunoblot-images used for the quantitative analysis in Figs. 6a and Fig. 7. The immunob...
Amyotrophic Lateral Sclerosis (ALS) is an adult-onset and fast progression neurodegenerative disease...
Figure S4. Pacer levels and localization in the spinal cord of presymptomatic SOD1G93A transgenic mi...
Figure S2. Pacer is expressed in neurons in the spinal cord of wild-type mice a, mRNA levels of Pace...
Figure S5. Pacer is expressed in MMP9-positive cells in the presymptomatic spinal cord of SOD1G93A t...
Figure S6. Pacer depletion results in detergent insoluble SOD1 aggregate accumulation. a-b, Densiome...
Figure S7. Depletion of Pacer leads to SOD1 aggregate accumulation. a, NSC34 cells were transiently ...
Table S3. Clinical and histopathological data of control and sporadic ALS cases. (DOCX 58 kb
Figure S1. ALS convergent analysis subnetworks. a-l, ALS disease subnetworks generated by IPA as an ...
Abstract Background Amyotrophic lateral sclerosis (ALS) is a multifactorial fatal motoneuron disease...
BackgroundAmyotrophic lateral sclerosis (ALS) is a multifactorial fatal motoneuron disease without a...
BackgroundAmyotrophic lateral sclerosis (ALS) is a multifactorial fatal motoneuron disease without a...
Figure S2. Whole transverse sectional images of the lumbar spinal cord in Figs. 2, 3 and 4. a Whole ...
Figure S6. Analysis autophagy in ventral midbrain of WT and AQP4 mice following injection of PBS or ...
Figure S1. APA Heat map for the ten genes that undergo shortening of their 3’UTRs and ten genes that...
Figure S4. Immunoblot-images used for the quantitative analysis in Figs. 6a and Fig. 7. The immunob...
Amyotrophic Lateral Sclerosis (ALS) is an adult-onset and fast progression neurodegenerative disease...
Figure S4. Pacer levels and localization in the spinal cord of presymptomatic SOD1G93A transgenic mi...
Figure S2. Pacer is expressed in neurons in the spinal cord of wild-type mice a, mRNA levels of Pace...
Figure S5. Pacer is expressed in MMP9-positive cells in the presymptomatic spinal cord of SOD1G93A t...
Figure S6. Pacer depletion results in detergent insoluble SOD1 aggregate accumulation. a-b, Densiome...
Figure S7. Depletion of Pacer leads to SOD1 aggregate accumulation. a, NSC34 cells were transiently ...
Table S3. Clinical and histopathological data of control and sporadic ALS cases. (DOCX 58 kb
Figure S1. ALS convergent analysis subnetworks. a-l, ALS disease subnetworks generated by IPA as an ...
Abstract Background Amyotrophic lateral sclerosis (ALS) is a multifactorial fatal motoneuron disease...
BackgroundAmyotrophic lateral sclerosis (ALS) is a multifactorial fatal motoneuron disease without a...
BackgroundAmyotrophic lateral sclerosis (ALS) is a multifactorial fatal motoneuron disease without a...
Figure S2. Whole transverse sectional images of the lumbar spinal cord in Figs. 2, 3 and 4. a Whole ...
Figure S6. Analysis autophagy in ventral midbrain of WT and AQP4 mice following injection of PBS or ...
Figure S1. APA Heat map for the ten genes that undergo shortening of their 3’UTRs and ten genes that...
Figure S4. Immunoblot-images used for the quantitative analysis in Figs. 6a and Fig. 7. The immunob...
Amyotrophic Lateral Sclerosis (ALS) is an adult-onset and fast progression neurodegenerative disease...