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pro vyhledávání: '"Jacqueline G, Lu"'
Publikováno v:
Sci Transl Med
Mutations in β-amyloid (Aβ) precursor protein (APP) cause familial Alzheimer’s disease (AD) probably by enhancing Aβ peptides production from APP. An antibody targeting Aβ (aducanumab) was approved as an AD treatment; however, some Aβ antibodi
Publikováno v:
Science Translational Medicine. 14
Mutations in β-amyloid (Aβ) precursor protein ( APP ) cause familial Alzheimer’s disease (AD) probably by enhancing Aβ peptides production from APP. An antibody targeting Aβ (aducanumab) was approved as an AD treatment; however, some Aβ antibo
Autor:
Jacqueline G, Lu, Juliet, Bishop, Sarah, Cheyette, Igor B, Zhulin, Su, Guo, Nara, Sobreira, Steven E, Brenner
Publikováno v:
Cold Spring Harbor Molecular Case Studies
Paroxysmal kinesigenic dyskinesia (PKD) is a rare neurological disorder characterized by recurrent attacks of dyskinetic movements without alteration of consciousness that are often triggered by the initiation of voluntary movements. Whole-exome sequ
Autor:
Juliet Chhay Bishop, Jacqueline G. Lu, Sarah R. Cheyette, Igor B. Zhulin, Nara Sobreira, Su Guo, Steven E. Brenner
Publikováno v:
Molecular Case Studies. 4:a002287
Paroxysmal kinesigenic dyskinesia (PKD) is a rare neurological disorder characterized by recurrent attacks of dyskinetic movements without alteration of consciousness that are often triggered by the initiation of voluntary movements. Whole-exome sequ