搜索页_ JB6 P+

常用资源

电子图书

期刊论文

学位会议

外文资源

特色专题

内部出版物

中国地质文献-中文(1)	CNKI会议论文(9)	CNKI期刊论文0611(25)	万方学位论文(1)
万方学术会议(1)	CNKI学位论文(4774)	知网期刊论文(5848)

在“Elsevier电子期刊”中，命中：915条，耗时：0.0179928 秒

在所有数据库中总计命中：10,659条

1.First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss

作者：Walid AL-Achkarp> ; p>p>ascientific14@aec.org.syp> ; Bassel AL-Halabi ; Bashar Ali ; Faten Moassass

关键词：Non- syndromic hearing loss (NSHL) ; GJB2 ; IVS1+1G>A ; GJB6 ; Syrian

刊名：International Journal of Pediatric Otorhinolaryngology

出版年：2017

2.Use of potential dietary phytochemicals to target miRNA: Promising option for breast cancer prevention and treatment?

作者：Md. Abu Sayeedp> ; p>p>m.a.sayeed@pm.univpm.itp> ; Massimo Bracci ; Raffaella Lazzarini ; Marco Tomasetti ; Monica Amati ; Guendalina Lucarini ; Roberto Di Primio ; Lory Santarelli

关键词：ALDH1 ; aldehyde dehydrogenase 1 ; AKT ; protein kinase B ; ARID4B ; AT-rich interactive domain-containing protein 4B ; BMI1 ; B-lymphoma Moloney murine leukemia virus insertion region-1 ; BMP1 ; bone morphogenetic protein 1 ; BRCA1 ; breast cancer 1 ; BIRC6 ; baculoviral IAP repeat-containing protein 6 ; CDC42 ; cell division cycle 42 ; CXCR4 ; C-X-C chemokine receptor type 4 ; CD1/24/44/49f ; cluster of differentiation 1/24/44/49f ; CRIP2 ; cysteine-rich protein 2 ; DNAJB6 ; DnaJ homolog subfamily B member 6 ; ER-α

刊名：Journal of Functional Foods

出版年：2017

3.Special purpose entities and bank loan contracting

作者：Jeong-Bon Kimp>ap>p> ; p>p>jb6kim@uwaterloo.cap> ; Byron Y. Songp>bp>p> ; p>p>yangsong@hkbu.edu.hkp> ; Zheng Wangp>cp>p> ; p>p>zwang22@cityu.edu.hkp>

关键词：Special purpose entity ; Loan contracting ; Information risk ; Earnings management

刊名：Journal of Banking & Finance

出版年：2017

4.Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes

作者：Sabina Pena B. Pê ; go ; DDS ; PhDp>ap>p> ; p>p>sabinapego@yahoo.com.brp> ; Ricardo D. Coletta ; DDS ; PhDp>bp> ; Simona Dumitriu ; MD ; PhDp>cp> ; Daniela Iancu ; MD ; PhDp>cp> ; Saleh Albanyan ; MDp>cp> ; Robert Kleta ; MD ; PhDp>cp> ; Maria Teresa Auricchio ; PhDp>dp> ; Luis Antô ; nio Santos ; DDS ; PhDp>ap> ; Breno Rocha ; DDSp>ap> ; Hercí ; lio Martelli-Jú ; nior ; DDS ; PhDp>ap>

刊名：Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology

出版年：2017

5.Phenotype in a patient with p.D50N mutation in GJB2 gene resemble both KID and Clouston syndromes

作者：T.G. Markovap>ap>p> ; p>p>1p>p> ; p>p>tmarkova@audiology.ru" class="auth_mail" title="E-mail the corresponding authorp> ; N.B. Brazhkinap>bp>p> ; p>p>2p> ; E.A. Bliznechp>cp>p> ; p>p>3p>p> ; p>p>bliznetzelena@mail.ru" class="auth_mail" title="E-mail the corresponding authorp> ; V.V. Bakhshinyanp>dp>p> ; p>p>4p>p> ; p>p>bakhshinyan@yahoo.com" class="auth_mail" title="E-mail the corresponding authorp> ; A.V. Polyakovp>cp>p> ; p>p>5p>p> ; p>p>apol@dnalab.ru" class="auth_mail" title="E-mail the corresponding authorp> ; G.A. Tavartkiladzep>ep>p> ; p>p>gtavartkiladze@audiology.ru" class="auth_mail" title="E-mail the corresponding authorp>

关键词：Hereditary hearing loss ; Keratitis&ndash ; ichthyosis&ndash ; deafness syndrome ; Clouston syndrome ; GJB2 and GJB6 gene mutation ; Connexin26

刊名：International Journal of Pediatric Otorhinolaryngology

出版年：2016

6.The S/T-Rich Motif in the DNAJB6 Chaperone Delays Polyglutamine Aggregation and the Onset of Disease in a Mouse Model

作者：Vaishali Kakkarp>1p> ; Cecilia Må ; nssonp>2p> ; Eduardo P. de Mattosp>1p>p> ; p>p>3p> ; Steven Berginkp>1p> ; Marianne van der Zwaagp>1p> ; Maria A.W.H. van Waardep>1p> ; Niels J. Kloosterhuisp>4p> ; Ronald Melkip>5p> ; Remco T.P. van Cruchtenp>2p> ; Salam Al-Karadaghip>2p> ; Paolo Arosiop>6p> ; Christopher M. Dobsonp>6p> ; Tuomas P.J. Knowlesp>6p> ; Gillian P. Batesp>7p> ; Jan M. van Deursenp>8p> ; Sara Linsep>2p> ; Bart van de Sluisp>4p> ; Cecilia Emanuelssonp>2p>p> ; p>p>9p> ; Harm H. Kampingap>1p>p> ; p>p>9p>p> ; p>p>h.h.kampinga@umcg.nl" class="auth_mail" title="E-mail the corresponding authorp>

刊名：Molecular Cell

出版年：2016

7.A novel mutation in DNAJB6, p.(Phe91Leu), in childhood-onset LGMD1D with a severe phenotype

作者：Tai-Seung Namp>ap>p> ; p>p>1p> ; Wenting Lip>bp>p> ; p>p>1p> ; Suk-Hee Heop>cp> ; Kyung-Hwa Leep>dp> ; Anna Chop>ep> ; Jin-Hong Shinp>fp> ; Young Ok Kimp>gp> ; Jong-Hee Chaep>hp> ; Dae-Seong Kimp>fp> ; Myeong-Kyu Kimp>ap>p> ; p>p>mkkim@jnu.ac.kr" class="auth_mail" title="E-mail the corresponding authorp> ; Seok-Yong Choip>bp>p> ; p>p>zebrafish@chonnam.ac.kr" class="auth_mail" title="E-mail the corresponding authorp>

关键词：Limb-girdle muscular dystrophy ; DNAJB6 ; Zebrafish ; Magnetic resonance imaging ; Human genetics

刊名：Neuromuscular Disorders

出版年：2015

8.Epigenetic modifications of triterpenoid ursolic acid in activating Nrf2 and blocking cellular transformation of mouse epidermal cells

作者：Hyuck Kimp>ap>p> ; p>p>bp>p> ; p>p>1p> ; Christina N. Ramirezp>bp>p> ; p>p>cp>p> ; p>p>1p> ; Zheng-Yuan Sup>dp> ; Ah-Ng Tony Kongp>ap>p> ; p>p>bp>p> ; p>p>KongT@pharmacy.rutgers.edu" class="auth_mail" title="E-mail the corresponding authorp>

关键词：UA ; Nrf2 ; JB6 P+ ; DNMT ; HDAC ; Skin cancer

刊名：Journal of Nutritional Biochemistry

出版年：2016

9.Superior electrochemical performance of non-precious Co-Ni-Mo alloy catalyst-impregnated Sr₂FeMoO_6-δ as an electrode material for symmetric solid oxide fuel cells

作者：Manasa K. Rathp>ap> ; Ki-Tae Leep>ap>p> ; p>p>bp>p> ; p>p>ktlee71@jbnu.ac.kr" class="auth_mail" title="E-mail the corresponding authorp>

关键词：Solid oxide fuel cell ; Oxide anode ; Double perovskite ; Impregnation ; Symmetric solid oxide fuel cells

刊名：Electrochimica Acta

出版年：2016

10.Novel mutations in DNAJB6 gene cause a very severe early-onset limb-girdle muscular dystrophy 1D disease

作者：Johanna Palmiop>ap>p> ; p>p>johanna.palmio@uta.fi" class="auth_mail" title="E-mail the corresponding authorp> ; Per Harald Jonsonp>bp> ; Anni Evilä ; p>bp> ; Mari Auranenp>cp> ; Volker Straubp>dp> ; Kate Bushbyp>dp> ; Anna Sarkozyp>dp> ; Sari Kiuru-Enarip>cp> ; Satu Sandellp>ap>p> ; p>p>ep> ; Helena Pihkop>fp> ; Peter Hackmanp>bp> ; Bjarne Uddp>ap>p> ; p>p>bp>p> ; p>p>gp>

关键词：Limb-girdle muscular dystrophy ; DNAJB6 gene ; Childhood-onset

刊名：Neuromuscular Disorders

出版年：2015

按检索点细分(915)

题名(55)

作者(9)

关键词(127)

文摘(691)

按出版年细分(915)

2027年及以后(9)

2017年(4)

2016年(16)

2015年(6)

2013年(27)

2012年(21)

2011年(26)

2010年(24)

2009年(29)

2008年(98)

2007年(116)

2006年(181)

2005年(80)

2004年(49)

2003年(7)

2002年(30)

2001年(5)

2000年(11)

2000年及以前(176)

地址：北京市海淀区学院路29号邮编：100083

电话：办公室：(+86 10)66554848；文献借阅、咨询服务、科技查新：66554700