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pro vyhledávání: '"B. J. Zeng"'
Akademický článek
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Publikováno v:
Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]. 55(5)
To explore the expression of p62 protein in lung adenocarcinoma (LUAD). In this study, a cross-sectional study was adopted. From December 2011 to May 2013, 60 patients with lung adenocarcinoma who were diagnosed and treated in Tongji Hospital of Tong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1cfcfce2597e3e64b2ad5baf51b6580b
https://pubmed.ncbi.nlm.nih.gov/34034412
https://pubmed.ncbi.nlm.nih.gov/34034412
Publikováno v:
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences. 50(3)
To evaluate the effect of the vacuum-formed retainer on preventing the proximal contact loss between the implant supported crown and its adjacent natural teeth.Forty-six posterior implant crowns in the mandible including 92 interproximal contacts in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c640111c0a424e8a4241cd2f6056c675
https://pubmed.ncbi.nlm.nih.gov/29930429
https://pubmed.ncbi.nlm.nih.gov/29930429
Publikováno v:
Biochemistry (Moscow). 78:721-725
The lysosomal storage disorders (LSD) represent a heterogeneous group of inherited diseases characterized by the accumulation of non-metabolized macromolecules (by-products of cellular turnover) in different tissues and organs. LSDs primarily develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e1c4b0a63820eade1409cab23a2cd2a
https://doi.org/10.1134/s0006297913070043
https://doi.org/10.1134/s0006297913070043
Akademický článek
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Publikováno v:
Insect molecular biology. 24(5)
The Spodoptera litura sterol carrier protein x (SlSCPx) gene is expressed in various tissues throughout the life cycle and plays important role in sterol absorption and transport. In this study, the effects of insect hormones (20-hydroexcdysone and j
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7263b4d5c49d8f3859e4eba509326ca7
https://pubmed.ncbi.nlm.nih.gov/26174044
https://pubmed.ncbi.nlm.nih.gov/26174044
Autor:
Paola Leone, Paola Torres, Edwin H. Kolodny, G. M. Pastores, Srinivasa S. Raghavan, Zhao-Hui Wang, B. J. Zeng
Publikováno v:
Molecular Genetics and Metabolism. 89:156-163
Canavan disease (CD), an autosomal recessive neurodegenerative disorder, is caused by mutations in the aspartoacylase (ASPA) gene. In the present study, the ASPA gene was analyzed in 24 non-Jewish patients with CD from 23 unrelated families. Within t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6980fdb47c6f0be690f4ece4ceecc1e
https://doi.org/10.1016/j.ymgme.2006.05.014
https://doi.org/10.1016/j.ymgme.2006.05.014
Autor:
Srinivasa S. Raghavan, R. De Gasperi, Zhao-Hui Wang, S. J. Kim, Edwin H. Kolodny, L. A. Ribeiro, B. J. Zeng, E. O. Ong, Gregory M. Pastores, Paola Leone
Publikováno v:
Journal of Inherited Metabolic Disease. 25:557-570
Canavan disease, an inherited leukodystrophy, is caused by mutationsin the aspartoacylase (ASPA) gene. It is most common among children of Ashkenazi Jewish descent but has been diagnosed in many diverse ethnic groups.Two mutations comprise the majori
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::720bf67ab5c93f60be1f59c7cebda01c
https://doi.org/10.1023/a:1022091223498
https://doi.org/10.1023/a:1022091223498
Autor:
Gregory M. Pastores, N Raksadawan, Y Ji, Edwin H. Kolodny, B. J. Zeng, Zhao-Hui Wang, Thomas Wisniewski, W Shan
Publikováno v:
Neuroscience. 113:629-640
Tyrosine hydroxylase (TH) and brain-derived neurotrophic factor (BDNF), expressed in normal astrocytes, were used in combination for the treatment of Parkinson's disease (PD) symptoms in a rat model. Normal neonatal rat astrocytes were co-transfected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6705cd5e1e1d4c663927baf7cb7dbd9
https://doi.org/10.1016/s0306-4522(02)00204-x
https://doi.org/10.1016/s0306-4522(02)00204-x
Autor:
Alex R. Paciorkowski, Paola Torres, B. J. Zeng, Swati Sathe, Edwin H. Kolodny, Sally S. Rosengren
Publikováno v:
Pediatric Neurology. 38:284-286
G(M2)-gangliosidosis is a neurodegenerative lysosomal disease with several clinical variants. We describe a 2-year-old black child with juvenile-onset disease, who presented with abnormal eye movements and cherry-red spots of the maculae. Mutation an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f2550ab8bc023f52359cb890fcadd5d
https://doi.org/10.1016/j.pediatrneurol.2007.12.004
https://doi.org/10.1016/j.pediatrneurol.2007.12.004