Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Yan-Yan Xue"'
Autor:
Rong‐Rong Lin, Lu‐Lu Jin, Yan‐Yan Xue, Zhe‐Sheng Zhang, Hui‐Feng Huang, Dian‐Fu Chen, Qian Liu, Zheng‐Wei Mao, Zhi‐Ying Wu, Qing‐Qing Tao
Publikováno v:
Advanced Science, Vol 11, Iss 24, Pp n/a-n/a (2024)
Abstract The blood brain barrier (BBB) limits the application of most therapeutic drugs for neurological diseases (NDs). Hybrid cell membrane‐coated nanoparticles derived from different cell types can mimic the surface properties and functionalitie
Externí odkaz:
https://doaj.org/article/ee4f8ff681c04f27bd4f57306e42e74f
Autor:
Yan-Yan Xue, Hao-Ling Cheng, Hai-Lin Dong, Hou-Min Yin, Yun Yuan, Ling-Chao Meng, Zhi-Ying Wu, Hao Yu
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Charcot-Marie-Tooth (CMT) disease is a group of inherited peripheral neuropathies, which are subdivided into demyelinating and axonal forms. Biallelic mutations in POLR3B are the well-established cause of hypomyelinating leukodyst
Externí odkaz:
https://doaj.org/article/4d3ac404a0f84e209fcda2b393229cf9
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
PurposeBiomarkers used for predicting longitudinal cognitive change in Alzheimer’s disease (AD) continuum are still elusive. Tau pathology, neuroinflammation, and neurodegeneration are the leading candidate predictors. We aimed to determine these t
Externí odkaz:
https://doaj.org/article/4776bc3436d742f9a88175f5ef571823
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-4 (2021)
Abstract Background Morvan syndrome (MoS) is a rare autoimmune syndrome associated with antibodies against two kinds of potassium channel proteins, contactin associated protein-like 2 (CASPR2) and leucine-rich glioma inactivated protein 1 (LGI1). MoS
Externí odkaz:
https://doaj.org/article/5d12915b9c6b41168c5377c070e2d430
Publikováno v:
Frontiers in Aging Neuroscience, Vol 13 (2021)
Background: National Institute on Aging—Alzheimer's Association (NIA-AA) proposed the AT(N) system based on β-amyloid deposition, pathologic tau, and neurodegeneration, which considered the definition of Alzheimer's disease (AD) as a biological co
Externí odkaz:
https://doaj.org/article/58b59daad9ff4dc987b5f521330b2935
Publikováno v:
Brain Sciences, Vol 12, Iss 5, p 517 (2022)
PLA2G6-associated neurodegeneration (PLAN) is a rare autosomal recessive disorder caused by PLA2G6 mutations. This study aimed to investigate the clinical characteristics and mutation spectrum of PLAN and to investigate the founder effects in Chinese
Externí odkaz:
https://doaj.org/article/4577672bb20c400b8e24cdd00df6684f
Autor:
Hong-Rong Cheng, Rong-Rong Lin, Hong-Lei Li, Yan-Yan Xue, Pei-Rong Gao, Dian-Fu Chen, Qing-Qing Tao, Zhi-Ying Wu
Publikováno v:
Neurobiology of Aging. 123:233-243
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::314ecaf8a09a799641fe37b4a4705fec
https://doi.org/10.1016/j.neurobiolaging.2022.12.009
https://doi.org/10.1016/j.neurobiolaging.2022.12.009
Autor:
Ke-Ke Zhang, Yu-Yang Wang, Qi Wang, Hao-Yue Wang, Yi-Zhuo Qian, Dian-Yun Zhang, Yan-Yan Xue, Shuai Li, Lei Zhang
Publikováno v:
Instrumentation Science & Technology. :1-16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b08d61ebe1c3d3a55b3bf79874eccf8d
https://doi.org/10.1080/10739149.2023.2180030
https://doi.org/10.1080/10739149.2023.2180030
Publikováno v:
Immunologic Research. 70:392-399
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75c0f6f8f08edc3fc777d67ed7cecf81
https://doi.org/10.1007/s12026-022-09276-x
https://doi.org/10.1007/s12026-022-09276-x
Publikováno v:
CNS Neuroscience & Therapeutics
A 37‐year old man presented a slight delay in early developmental milestones, cognitive decline, difficulty walking, cerebellar signs and extrapyramidal signs. Brain magnetic resonance imaging (MRI) showed a thin corpus callosum, cerebral atrophy,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d72dde3a4610b42f6edcd14920423cea
https://doi.org/10.1111/cns.13723
https://doi.org/10.1111/cns.13723