| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/ANA.21070 |
| P698 | PubMed publication ID | 17387721 |
| P50 | author | Daisuke Ito | Q30430138 |
| Norihiro Suzuki | Q30430157 | ||
| P2860 | cites work | Transient, lectin-like association of calreticulin with folding intermediates of cellular and viral glycoproteins | Q34451461 |
| The unfolded protein response--a stress signaling pathway of the endoplasmic reticulum | Q35885345 | ||
| Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation | Q38720406 | ||
| P433 | issue | 3 | |
| P921 | main subject | pathogenesis | Q372016 |
| P304 | page(s) | 237-250 | |
| P577 | publication date | 2007-03-01 | |
| P1433 | published in | Annals of Neurology | Q564414 |
| P1476 | title | Molecular pathogenesis of seipin/BSCL2-related motor neuron diseases | |
| P478 | volume | 61 |
| Q42436840 | A new seipin-associated neurodegenerative syndrome |
| Q37378320 | A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier? |
| Q37234369 | A role for ubiquitin ligases and Spartin/SPG20 in lipid droplet turnover |
| Q39293392 | ALS and MMN mimics in patients with BSCL2 mutations: the expanding clinical spectrum of SPG17 hereditary spastic paraplegia |
| Q39224170 | Alleviation of seipinopathy-related ER stress by triglyceride storage. |
| Q42940304 | Characterization of alternative isoforms and inclusion body of the TAR DNA-binding protein-43. |
| Q27325515 | Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary Neuropathy |
| Q31059435 | Clinical and laboratory data of a large series of patients with congenital generalized lipodystrophy |
| Q46327262 | Echinacoside's nigrostriatal dopaminergic protection against 6-OHDA-Induced endoplasmic reticulum stress through reducing the accumulation of Seipin |
| Q45232740 | Evidence of a link between ubiquilin 2 and optineurin in amyotrophic lateral sclerosis |
| Q58553718 | Exploring Seipin: From Biochemistry to Bioinformatics Predictions |
| Q37325080 | Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms |
| Q37817723 | Hereditary spastic paraplegias: membrane traffic and the motor pathway |
| Q37136953 | Interaction of the vitamin D receptor with a vitamin D response element in the Mullerian-inhibiting substance (MIS) promoter: regulation of MIS expression by calcitriol in prostate cancer cells |
| Q47900941 | Lack of seipin in neurons results in anxiety- and depression-like behaviors via down regulation of PPARγ. |
| Q35561950 | Molecular characterization of seipin and its mutants: implications for seipin in triacylglycerol synthesis |
| Q36733211 | Motor neuron degeneration in a mouse model of seipinopathy. |
| Q51751501 | Mutant SOD1 inhibits ER-Golgi transport in amyotrophic lateral sclerosis. |
| Q34438424 | Neuroanatomical characterisation of the expression of the lipodystrophy and motor-neuropathy gene Bscl2 in adult mouse brain |
| Q90286752 | Neurochemical Characterization of Brainstem Pro-Opiomelanocortin Cells |
| Q52607544 | Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS. |
| Q58578562 | Phenotypic and Genetic Characteristics of Lipodystrophy: Pathophysiology, Metabolic Abnormalities, and Comorbidities |
| Q64064600 | Promethin Is a Conserved Seipin Partner Protein |
| Q37522718 | Re-analysis of an original CMTX3 family using exome sequencing identifies a known BSCL2 mutation |
| Q37186867 | Recent advances in the genetics of spastic paraplegias |
| Q34304833 | Roles of ataxin-2 in pathological cascades mediated by TAR DNA-binding protein 43 (TDP-43) and Fused in Sarcoma (FUS) |
| Q34905160 | Seipin Is a Discrete Homooligomer |
| Q34474731 | Seipin is necessary for normal brain development and spermatogenesis in addition to adipogenesis |
| Q51791668 | Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes. |
| Q35958418 | Seipin: from human disease to molecular mechanism |
| Q28293837 | Seipinopathy: a novel endoplasmic reticulum stress-associated disease |
| Q36071217 | Skipped BSCL2 Transcript in Celia's Encephalopathy (PELD): New Insights on Fatty Acids Involvement, Senescence and Adipogenesis |
| Q38761524 | TFG-Related Neurologic Disorders: New Insights Into Relationships Between Endoplasmic Reticulum and Neurodegeneration |
| Q89207801 | Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients |
| Q47943026 | The Lipid Droplet and the Endoplasmic Reticulum |
| Q27015793 | The delicate balance between secreted protein folding and endoplasmic reticulum-associated degradation in human physiology |
| Q52145718 | The expression of SEIPIN in the mouse central nervous system. |
| Q36807635 | The human lipodystrophy gene BSCL2/seipin may be essential for normal adipocyte differentiation |
| Q27932399 | The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology |
| Q34278915 | Towards a mechanistic understanding of lipodystrophy and seipin functions |
Search more.