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8 documents found
1: Title: Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies.
Authors: Yamada, Yoshiji, et.al. .
Journal: International journal of molecular medicine (Int J Mol Med), Vol. 39 (5): 1091-1100, 2017 .
Snippet: Examination of the correlation of these latter 8 SNPs to true or dissecting aortic aneurysm separately showed that rs1465567 [T/C (W229R)] of the EGF-like, fibronectin type III, and laminin G domains gene (EGFLAM) (dominant model; P=0.0014; odds ratio, 1.63) was significantly (P<0.0016)
Affiliation: Department of Human Functional Genomics, Advanced Science Research Promotion Center, Mie University, Tsu, Mie 514-8507, Japan. CREST, Japan Science and Technology Agency, Kawaguchi 332-0012, Japan. Department of Cardiovascular Medicine, Inabe General Hospital, Inabe 511-0428, Japan. Department of Cardiovascular Medicine, Gifu Prefectural Tajimi Hospital, Tajimi 507-8522, Japan. Department of Molecular Epidemiology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo 101-0062, Japan. Section of Molecular Pathology, Graduate School of Health Care Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan. Research Team for Social Participation and Community Health, Tokyo Metropolitan Institute of Gerontology, Tokyo 173-0015, Japan. Research Team for Promoting Support System for Home Care, Tokyo Metropolitan Institute of Gerontology, Tokyo 173-0015, Japan. Research Team for Social Participation and Health Promotion, Tokyo Metropolitan Institute of Gerontology, Tokyo 173-0015, Japan. Center for Promotion of Clinical Investigation, Tokyo Metropolitan Geriatric Hospital, Tokyo 173-0015, Japan. Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Tokyo 173-0015, Japan. Department of Clinical Laboratory, Tokyo Metropolitan Geriatric Hospital, Tokyo 173-0015, Japan. .
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2: Title: High-risk oral leukoplakia is associated with aberrant promoter methylation of multiple genes.
Authors: Abe, Masanobu, et.al. .
Journal: BMC cancer, Vol. 16, 2016 .
Snippet: In OSCC tissues (n = 26), 8 of the 13 genes, TSPYL5, EGFLAM, CLDN11, NKX2-3, RBP4, CMTM3, TRPC4, and MAP6, were methylated.
Affiliation: Department of Oral & Maxillofacial Surgery, University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan. abem-ora@h.u-tokyo.ac.jp. Division for Health Service Promotion, University of Tokyo, Tokyo, Japan. abem-ora@h.u-tokyo.ac.jp. Division of Epigenomics, National Cancer Center Research Institute, Tokyo, Japan. Department of Dentistry, Oral & Maxillofacial Surgery, Jichi Medical University, Tochigi, Japan. Department of Oral & Maxillofacial Surgery, University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan. .
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3: Title: [Cinical and genetic characteristics of familial Meniere's disease: three families report].
Authors: Gao, Yun, et.al. .
Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery (Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi), Vol. 50 (11): 915-24, 2015 .
Snippet: 2057G>A in EGFLAM and c. 1961C>T in ITGA8.
Affiliation: Department of Otorhinolaryngology Head and Neck Surgery, Institute of Otorhinolaryngology, Chinese People's Liberation Army General Hospital, Beijing 100853, China. Email: sxzent@163.com, Department of Otorhinolaryngology Head and Neck Surgery, General Hospital of Chinese People's Armed Police Forces, Beijing 100039, China. Email: wqcr@263.net. .
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4: Title: Transcriptome comparisons identify new cell markers for theca interna and granulosa cells from small and large antral ovarian follicles.
Authors: Hatzirodos, Nicholas, et.al. .
Journal: PloS one, Vol. 10 (3): e0119800, 2015 .
Snippet: Many genes up regulated in theca interna were common to both sizes of follicles (MGP, DCN, ASPN, ALDH1A1, COL1A2, FN1, COL3A1, OGN, APOD, COL5A2, IGF2, NID1, LHFP, ACTA2, DUSP12, ACTG2, SPARCL1, FILIP1L, EGFLAM, ADAMDEC1, HPGD, COL12A1, FBLN5, RAMP2, COL15A1, PLK2, COL6A3, LOXL1, RARRES1, FLI1, LAMA2).
Affiliation: Discipline of Obstetrics and Gynaecology, School of Paediatrics and Reproductive Health, Robinson Research Institute, University of Adelaide, Adelaide, South Australia, 5005, Australia. School of Medical Science, Griffith University, Gold Coast, 4222, Queensland, Australia. .
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5: Title: Rabbit morula vitrification reduces early foetal growth and increases losses throughout gestation.
Authors: Vicente, J S, et.al. .
Journal: Cryobiology, Vol. 67 (3): 321-6, 2013 .
Snippet: We observed that the relative expressions of mRNA transcripts from SCGB1A1, EMP1, ANXA3 and EGFLAM genes were significantly altered.
Affiliation: Instituto de Ciencia y Tecnología Animal, Universidad Politécnica de Valencia, 46022 Valencia, Spain. Electronic address: jvicent@dca.upv.es. .
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6: Title: Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.
Authors: Adkins, D E, et.al. .
Journal: Translational psychiatry (Transl Psychiatr), Vol. 2, 2012 .
Snippet: Suggestive findings were also found for SNPs at LAMA1, AOX2P, EGFLAM, FHIT and RTP2.
Affiliation: Center for Biomarker Research and Personalized Medicine, Virginia Commonwealth University, School of Pharmacy, Richmond, VA 23298-0581, USA. deadkins@vcu.edu .
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7: Title: Familial brain arteriovenous malformation maps to 5p13-q14, 15q11-q13 or 18p11: linkage analysis with clipped fingernail DNA on high-density SNP array.
Authors: Oikawa, Masahiro, et.al. .
Journal: European journal of medical genetics (Eur J Med Genet), Vol. 53 (5): 244-9, 2010 Sep-Oct .
Snippet: such as MAP3K1, DAB2, OCLN, FGF10, ESM1, ITGA1, ITGA2, EGFLAM, ERBB2IP, and PIK3R1, but no causative genetic alteration was detected.
Affiliation: Departments of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan. .
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8: Title: [Model of aberrant DNA methylation patterns and its applications in epithelial ovarian cancer.].
Authors: Gu, Xiao-Hong, et.al. .
Journal: Zhonghua fu chan ke za zhi, Vol. 44 (10): 754-9, 2009 .
Snippet: The methylation ratio of gene LSM2, EGFLAM and CDKN2A in tissue DNA of patients with epithelial ovarian cancer and benign ovarian diseases was 11% (10/87) versus 33% (14/42), 8% (7/87) versus 21% (9/42), 9% (8/87) versus 31% (13/42), respectively, which was significantly decreased in tissues DNA of ovarian cancer than that from benign ovarian diseases (P < 0.05).
Affiliation: Department of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai 200032, China. .
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