refine search
Authors
Locations
Journals
Publication Dates
Find concepts in Knowledge Base
Explore current query
documentsstatisticstop authorclipboard
7 documents found
1: Title: Downregulation and Aberrant Localization of Forkhead Box J1 in Allergic Nasal Mucosa.
Authors: Peng, Yang, et.al. .
Journal: International archives of allergy and immunology (Int Arch Allergy Immunol), 2018 .
Snippet: We developed a semiquantitative scoring system to elucidate their localization in 5 areas per paraffin section, with individual sections being assigned a score between 0 and 2. RESULTS: The mRNA levels of FOXJ1, DNAI1, DNALI1, and DNAH9 were significantly reduced in patients with AR compared with controls (all p < 0.05).
Affiliation: Department of Otolaryngology, The Second School of Clinical Medicine, Southern Medical University, Guangzhou, China. Department of Otolaryngology Head and Neck Surgery, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China. Department of Otolaryngology, National University of Singapore, National University Health System, Singapore, Singapore. Department of Otolaryngology - Head and Neck Surgery, First Affiliated Hospital, Zhengzhou University, Zhengzhou, China. State Key Laboratory of Respiratory Disease, National Clinical Research Center of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China. Department of Otolaryngology - Head and Neck Surgery, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, China. Department of Otolaryngology, The Second Hospital of Shandong University, Jinan, China. Department of Otorhinolaryngology - Head and Neck Surgery, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China. Department of Otolaryngology, Zhujiang Hospital, Southern Medical University, Guangzhou, China. .
Related Products: order online
2: Title: Combined analysis of DNA methylation and gene expression profiles of osteosarcoma identified several prognosis signatures.
Authors: Tian, Wen, et.al. .
Journal: Gene, 2018 .
Snippet: Kaplan Meier analysis of OS genes identified BHMT2, DOCK2, DNALI1 and RIPK3 as significant OS survival-related genes.
Affiliation: Department of Internal Medicine-Oncology, Cangzhou Central Hospital, Cangzhou 061000, Hebei Province, China. Department of Internal Medicine-Oncology, Cangzhou Central Hospital, Cangzhou 061000, Hebei Province, China. Electronic address: jhgaoczch@hotmail.com. .
Related Products: order online
3: Title: ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.
Authors: Zariwala, Maimoona A, et.al. .
Journal: American journal of human genetics (Am J Hum Genet), Vol. 93 (2): 336-45, 2013 .
Snippet: Mutations in ZMYND10 result in the absence of the axonemal protein components DNAH5 and DNALI1 from respiratory cilia.
Affiliation: Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. .
Related Products: order online
4: Title: Clinical implications of gene dosage and gene expression patterns in diploid breast carcinoma.
Authors: Parris, Toshima Z, et.al. .
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research (Clin Cancer Res), Vol. 16 (15): 3860-74, 2010 .
Snippet: In addition, more malignant tumors with normal gene dosage levels displayed a recurrent overexpression of UBE2C, S100A8, and CBX2, and downregulation of LOC389033, STC2, DNALI1, SCUBE2, NME5, SUSD3, SERPINA11, AZGP1, and PIP.
Affiliation: Department of Oncology, Institute of Clinical Sciences, and Laboratory of Clinical Pathology and Cytology, Sahlgrenska Academy at University of Gothenburg, Gula stråket 2, Gothenburg, Sweden. toshima.parris@oncology.gu.se .
Related Products: order online
5: Title: Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects.
Authors: Loges, Niki Tomas, et.al. .
Journal: American journal of human genetics (Am J Hum Genet), Vol. 85 (6): 883-9, 2009 .
Snippet: Functional analyses showed that LRRC50 deficiency disrupts assembly of distally and proximally DNAH5- and DNAI2-containing ODA complexes, as well as DNALI1-containing IDA complexes, resulting in immotile cilia.
Affiliation: Department of Paediatrics and Adolescent Medicine, University Hospital 79106 Freiburg, Germany. .
Related Products: order online
6: Title: Gene expression analysis of frontotemporal lobar degeneration of the motor neuron disease type with ubiquitinated inclusions.
Authors: Mishra, Manjari, et.al. .
Journal: Acta neuropathologica (Acta Neuropathol), Vol. 114 (1): 81-94, 2007 .
Snippet: Dynein axonemal light intermediate chain 1 (DNALI1) (microtubule/cytoskeleton network associated) expression was 3-fold higher and myeloid differentiation primary response gene 88 (MYD88) (signal transduction network) was 3.3 times higher in FTLD-U than FTLD-MND and controls; annexin A2 (ANXA2) (endosomal sorting) expression was 11.3-fold higher in FTLD-U than FTLD-MND and 2.3-fold higher than controls.
Affiliation: Cognitive Neurology and Alzheimer Disease Center, Northwestern University, Feinberg School of Medicine, 320 East Superior St, Chicago, IL, 60611, USA. manjari@northwestern.edu .
Related Products: order online
7: Title: The murine Dnali1 gene encodes a flagellar protein that interacts with the cytoplasmic dynein heavy chain 1.
Authors: Rashid, Sajid, et.al. .
Journal: Molecular reproduction and development (Mol Reprod Dev), Vol. 73 (6): 784-94, 2006 .
Snippet: Antibodies were raised against a GST-Dnali1 fusion protein and used to localize Dnali1 within differentiating male germ cells.
Affiliation: Institute of Human Genetics, University of Goettingen, Goettingen, Germany. .
Related Products: order online
Documents per page: 20 | 50 | 100