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RAPSN Gene - GeneCards | RAPSN Protein | RAPSN Antibody
RAPSN Fusion Protein Ag13896 | Proteintech
Membraneless condensates by Rapsn phase separation as a platform for ...
RAPSN Polyclonal Antibody (PA5-58801)
RAPSN - Wikipedia
Sanger sequencing of the two RAPSN variants (p.Gln88Lys above and ...
Table 1 from Massive parallel sequencing identifies RAPSN and PDHA1 ...
RAPSN - LSBio
Lysosomal exocytosis was significantly increased in Rapsn −/− ...
RAPSN Monoclonal Antibody (1234) (MA1-746)
RAPSN Monoclonal Antibody (1234) | Invitrogen (MA1-746)
Schematic diagram and sequence of RAPSN amplicon. (A) The locations of ...
The power of the RAPSN methylation to distinguish LC cases from ...
RAPSN Polyclonal Antibody | Invitrogen (PA5-115824)
RAPSN antibody (20453-1-AP) | Proteintech
RAPSN Methylation Differences Between LC Cases and Controls (Age ...
A novel mutation in the TPR6 domain of the RAPSN gene associated with ...
RAPSN Gene Myasthenic Syndrome Congenital Type 11 Test - KSh 56,000 in ...
RAPSN - Alchetron, The Free Social Encyclopedia
Invitrogen RAPSN Polyclonal Antibody 100 μL | Buy Online | Invitrogen ...
RAPSN KO细胞 | CRISPR/Cas9 HEK 293敲除细胞系 – 艾迪基因
Individual clinical symptoms of the 10 patients harboring RAPSN ...
RAPSN mutations in the four white families* | Download Table
Haplotype analysis of 21 unrelated CMS patients (41 RAPSN N88K ...
RAPSN Polyclonal Antibody, Invitrogen™ 100 μL; Unconjugated Primary ...
Methylation levels of RPTOR (cg06418238), MGRN1 (cg00736299), RAPSN ...
Psychopharmacological treatments use in a RAPSN related Congenital ...
The Association Between RAPSN Methylation in Peripheral Blood and Earl ...
RAPSN antibody (20453-1-AP) | Proteintech | 武汉三鹰生物技术有限公司
Mutation Analysis of CHRNA1, CHRNB1, CHRND, and RAPSN Genes in Multiple ...
(PDF) The congenital myasthenic syndrome mutation RAPSN N88K derives ...
The Association Between RAPSN Methylation in Peripheral Blood and Early ...
WikiGenes - RAPSN - receptor-associated protein of the synapse
Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 ...
(PDF) E-box mutations in the RAPSN promoter region in eight cases with ...
Clustering acetylcholine receptors in neuromuscular junction by phase ...
(A) Transcriptional start sites of RAPSN. The major transcriptional ...
Issue: Neuron
Congenital Myasthenic Syndrome RAPSN-Associated - Congenital Myasthenic ...
小鼠突触受体关联蛋白(RAPSN)ELISA试剂盒使用说明书-小鼠突触受体关联蛋白(RAPSN)ELISA试剂盒操作注意事项
Anti-RAPSN Human Protein Atlas Antibody
Multiexon deletions account for 15% of congenital myasthenic syndromes ...
Cholinergic regulation of osteocyte mechanobiology: A paradigm for bone ...
A newly identified chromosomal microdeletion of the rapsyn gene causes ...
The diagnostic potential of the combined maker panel (RPTOR, MGRN1 and ...
A mechanism in agrin signaling revealed by a prevalent Rapsyn mutation ...
(PDF) Chronic stridor as an early presentation of congenital myasthenic ...
梅林/熊文诚等揭示突触后受体聚集和神经肌肉接头形成的新机制:Rapsn液-液相分离
Preimplantation genetic testing as a means of preventing hereditary ...