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Wiley电子期刊(1)	NATURE电子期刊(2)	ACS电子期刊(2)
SpringerLink电子期刊(86)	Elsevier电子期刊(98)

在“Elsevier电子期刊”中，命中：98条，耗时：小于0.01 秒

在所有数据库中总计命中：189条

1.Secondary Necrosis: Accidental No More

作者：Lorenzo Galluzzi¹ ; ² ; ³ ; ⁴ ; ⁵ ; ⁶ ; ^{deadoc@vodafone.it} ; Guido Kroemer² ; ³ ; ⁴ ; ⁵ ; ⁷ ; ⁸ ; ⁹

关键词：caspases ; danger signaling ; DFNA5 ; GSDMD ; necroptosis ; pyroptosis

刊名：Trends in Cancer

出版年：2017

2.Hollow crystalline straws of diclofenac for high-dose and carrier-free dry powder inhaler formulations

作者：Ashkan K. Yazdi ; ^{ashkan.k.yazdi@utexas.edu" class="auth_mail" title="E-mail the corresponding author} ; ^{ashkan.k.yazdi@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Hugh D.C. Smyth

关键词：DFNa ; diclofenac sodium ; DF ; diclofenac ; HCl ; hydrochloric acid ; SEM ; scanning electron microscopy ; BET ; Brunauer-Emmett-Teller ; SSA ; specific surface area ; FT-IR ; Fourier transform infrared spectroscopy ; XRD ; X-ray powder diffraction ; USP ; United States Pharmacopoeia ; ρB ; bulk density ; ρT ; tapped density ; ρ ; true density ; CI ; compressibility index ; HR ; Hausner ratio ; DSC ; differential scanning calorimetry ; HPMC ; hydroxypropyl methylcellulose ; NGI ; next generation impactor ; ED% ; emitted dose per

刊名：International Journal of Pharmaceutics

出版年：2016

3.A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9

作者：Masatsugu Masuda^a ; ^b ; ^{masoeur13@mac.com" class="auth_mail" title="E-mail the corresponding author} ; Hideki Mutai^a ; ^{mutaihideki@kankakuki.go.jp" class="auth_mail" title="E-mail the corresponding author} ; Yukiko Arimoto^c ; ^{y.armt1@pref.chiba.lg.jp" class="auth_mail" title="E-mail the corresponding author} ; Atsuko Nakano^c ; ^{a.nkn@pref.chiba.lg.jp" class="auth_mail" title="E-mail the corresponding author} ; Tatsuo Matsunaga^a ; ^d ; ^{matsunagatatsuo@kankakuki.go.jp" class="auth_mail" title="E-mail the corresponding author}

关键词：COCH ; DFNA9 ; Frameshift variant ; Haploinsufficiency ; Hearing loss

刊名：Biochemical and Biophysical Research Communications

出版年：2016

4.Genetic association of MYH genes with hereditary hearing loss in Korea

作者：Sang-Joo Kim^a ; ^b ; ¹ ; Seokwon Lee^a ; ^b ; ¹ ; Hong-Joon Park^c ; ¹ ; Tae-Hun Kang^a ; ^b ; Borum Sagong^a ; Jeong-In Baek^d ; Se-Kyung Oh^e ; Jae Young Choi^f ; Kyu-Yup Lee^g ; ^{kylee@knu.ac.kr" class="auth_mail" title="E-mail the corresponding author} ; Un-Kyung Kim^a ; ^b ; ^{kimuk@knu.ac.kr" class="auth_mail" title="E-mail the corresponding author}

关键词：NMMHC II-A ; Non-muscle myosin heavy chain IIA ; NMMHC II-C ; Non-muscle myosin heavy chain IIC ; ADNSHL ; Autosomal dominant non-syndromic hearing loss ; MYH9 ; Myosin ; heavy chain 9 ; non-muscle ; MHA ; May-Hegglin anomaly ; FTNS ; Fechtner syndrome ; SBS ; Sebastian syndrome ; EPS ; Epstein syndrome ; APS ; Alport syndrome ; MYH14 ; Myosin ; heavy chain 14 ; non-muscle ; DFNA ; Nonsyndromic deafness ; autosomal dominant ; PTA ; Pure-tone audiometry ; IRB ; The Institutional Review Board ; PCR ; Polymerase chain reaction ; R

刊名：Gene

出版年：2016

5.Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family

作者：Yalin Ma^a ; ^b ; ^c ; ¹ ; Yun Xiao^a ; ^b ; ¹ ; Fengguo Zhang^a ; ^b ; Yuechen Han^a ; ^b ; Jianfeng Li^a ; ^b ; Lei Xu^a ; ^b ; ^{sdphxl@126.com" class="auth_mail" title="E-mail the corresponding author} ; Xiaohui Bai^a ; ^b ; ^{sphbaixiaohui@163.com" class="auth_mail" title="E-mail the corresponding author} ; Haibo Wang^a ; ^b ; ^{wang.hb7585@hotmail.com" class="auth_mail" title="E-mail the corresponding author}

关键词：Deafness ; Autosomal recessive inheritance ; MYO7A gene ; Mutation

刊名：International Journal of Pediatric Otorhinolaryngology

出版年：2016

6.Despite a lack of otoacoustic emission, word recognition is not seriously influenced in a TECTA DFNA8/12 family

作者：Reinhard Ramsebner^a ; Martin Koenighofer^a ; Thomas Parzefall^a ; Trevor Lucas^b ; Christian Schoefer^b ; Klemens Frei^a ; ^{klemens.frei@meduniwien.ac.at" class="auth_mail}

关键词：DFNA8/12 ; p.Y1870C ; TECTA ; OAE ; Autosomal dominant ; Hearing impairment

刊名：International Journal of Pediatric Otorhinolaryngology

出版年：May, 2014

7.A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

作者：Amina Bakhchane^a ; Hicham Charoute^a ; Halima Nahili^a ; Rachida Roky^b ; Hassan Rouba^a ; Majida Charif^a ; ^c ; ^d ; Guy Lenaers^c ; ^d ; ¹ ; Abdelhamid Barakat^a ; ¹ ; ^{hamid.barakat@pasteur.ma" class="auth_mail" title="E-mail the corresponding author}

关键词：ARNSHL ; autosomal recessive non-syndromic hearing loss ; DFNA ; deafness ; autosomal dominant 36 ; DFNB ; deafness ; autosomal recessive ; ESP ; Exome Sequencing Project ; EVS ; Exome Variant Server ; GJB2 ; gap junction protein ; beta 2 ; 26 ; kDa ; LRTOMT ; leucine rich transmembrane and O-methyltransferase domain containing ; MT-RNR1 ; Ribosomal RNA ; Mitochondrial ; 12S ; PolyPhen ; Polymorphism Phenotyping ; SIFT ; Sorting Intolerant From Tolerant ; TMC1 ; transmembrane channel-like 1 ; WES ; Whole-exome sequencing

刊名：Gene

出版年：2015

8.Clinical characterization of a novel COCH mutation G87V in a Chinese DFNA9 family

作者：Dong-Ye Chen ; Yong-Chuan Chai ; Tao Yang ; Hao Wu

关键词：COCH ; DFNA9 ; Hearing impairment ; Vestibular dysfunction ; Novel mutation

刊名：International Journal of Pediatric Otorhinolaryngology

出版年：2013

9.Genetics of Hearing Loss—Nonsyndromic

作者：Kay W. Chang ; MD ^{kchang@ohns.stanford.edu" class="auth_mail" title="E-mail the corresponding author}

关键词：Nonsyndromic hearing loss ; DFNA ; DFNB ; GJB2 ; Next-generation sequencing ; Massively parallel sequencing

刊名：Otolaryngologic Clinics of North America

出版年：2015

10.Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1-2q23.3

作者：E. van Beelen^a ; ^b ; ^{E.vanBeelen@kno.umcn.nl} ; M. Schraders^a ; ^b ; ^c ; ^{M.Schraders@gen.umcn.nl} ; P.L.M. Huygen^a ; ^{P.Huygen@kno.umcn.nl} ; J. Oostrik^a ; ^b ; ^c ; ^{J.Oostrik@gen.umcn.nl} ; R.F. Plantinga^a ; ^{r.plantinga@cwz.nl} ; W. van Drunen^a ; R.W.J. Collin^c ; ^e ; ^{R.Collin@gen.umcn.nl} ; D.P. Kooper^d ; ^{kooper@rdgg.nl} ; R.J.E. Pennings^a ; ^b ; ^{R.Pennings@kno.umcn.nl} ; C.W.R.J. Cremers^a ; ^b ; ^{C.Cremers@kno.umcn.nl} ; H. Kremer^a ; ^b ; ^c ; ^e ; ^{H.Kremer@gen.umcn.nl} ; H.P.M. Kunst^a ; ^b ; ^{H.Kunst@kno.umcn.nl}

关键词：adNSHI ; autosomal dominant non-syndromic hearing impairment ; ARTA ; Age-related typical audiograms ; ATD ; Annual threshold deterioration ; cM ; Centimorgan ; dB ; Decibel ; HL ; Hearing Level ; kHz ; Kilohertz ; Mb ; Megabase ; PTA ; Pure tone average ; SNP ; Single nucl

刊名：Hearing Research

出版年：2013

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