Keywords: Lipid droplets; Seipin; Lipin; CDP-DAG synthase; AGPAT2; BSCL2; Lipodystrophy;
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: Seipin; BSCL2; Neurodegeneration; Lipodystrophy; Intranuclear inclusions; Progressive encephalopathy; Celia's encephalopathy; Oligomerization; Phenotype rescue;
Keywords: ACP33; Maspardin gene; AD; Autosomal dominant; AP4B1; Adaptor-related protein complex 4, epsilon 1 subunit gene; AP4M1; Adaptor-related protein complex 4, Mu 1 subunit gene; AP4E1; Adaptor-related protein complex 4, Epsilon 1 subunit gene; AP4S1; Adaptor-
Keywords: Acaca; Acetyl-Coenzyme A carboxylase 1; Acly; ATP citrate lyase; Actb; Beta-actin; ANOVA; Analysis of variance; AUC; Area under the curve; Bax; Bcl2-associated X protein; Bcl2; B cell leukemia/lymphoma 2; Bscl2; Berardinelli-Seip congenital lipodystroph
Adipose specific disruption of seipin causes early-onset generalised lipodystrophy and altered fuel utilisation without severe metabolic disease
Keywords: BSCL2; Seipin; CGL2; Lipodystrophy; Adipose tissue; Browning;
Part B: Morphometric and transcriptomic responses to sub-chronic exposure to the polycyclic aromatic hydrocarbon phenanthrene in the fathead minnow (Pimephales promelas)
Keywords: PNPLA2; patatin-like phospholipase domain containing 2; APOE; apolipoprotein E; NPC1; Niemann-Pick disease, type C1; LCAT; lecithin-cholesterol acyltransferase; DGAT1; diacylglycerol O-acyltransferase 1; LRP1; low density lipoprotein-related protein 1 (al
Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature review
Keywords: EEG; BSCL2; Berardinelli-Seip; Seipin;
The Vitotox and ToxTracker assays: A two-test combination for quick and reliable assessment of genotoxic hazards
Keywords: B[a]P; benzo[a]pyrene; Blvrb; biliverdin reductase B; Bscl2; berardinelli-seip congenital lipodystrophy 2; Btg2; B-cell translocation gene 2; CHF; chloramphenicol; CYC; cyclophosphamide; DAT; 2,4-diaminotoluene; Ddit3; DNA damage inducible transcript 3; G
Seipin oligomers can interact directly with AGPAT2 and lipin 1, physically scaffolding critical regulators of adipogenesis
Keywords: Lipodystrophy; BSCL2; AGPAT2; Lipin; Seipin; Lipid synthesis; Adipocyte; Adipogenesis; Atomic force microscopy (AFM)
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance
Keywords: ACP33; Maspardin gene; AD; Autosomal dominant; ALS; Amyotrophic lateral sclerosis; AP; Adaptor Protein complex; AR; Autosomal recessive; ATL1; Atlastin-1 gene; BMP; Bone morphogenic protein; BSCL2; Berardinelli-Seip congenital lipodystrophy gene; CYP7B1;
Lipodystrophies: Disorders of adipose tissue biology
Keywords: Lipodystrophy; AGPAT2; BSCL2; CAV1; LMNA; PPARG; AKT2; ZMPSTE24; Lipid droplet; Acyltransferase
Characterization of seipin/BSCL2, a protein associated with spastic paraplegia 17
Keywords: Seipin; BSCL2; Endoplasmic reticulum stress; Unfolded protein response; Motor neuron disease; Lipodystrophy
Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome
Keywords: Charcot–Marie–Tooth disease type 2D; CMT2; Distal hereditary motor neuropathy; dHMN; BSCL2; GARS; HSPB1, HSPB8
BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathy
Keywords: Spastic paraparesis; Silver syndrome; Hereditary motor neuropathy; BSCL2
Traffic accidents: Molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias
Keywords: Mitochondria; Transport; Axon; Degeneration; Golgi apparatus; Vesicle trafficking; Myelin; Endocytosis; Motor; Chaperone; BSCL2; Berardinelli-Seip congenital lipodystrophy 2; CGL; congenital generalized lipodystrophy; ER; endoplasmic reticulum; GEF; gua