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Springer电子图书(1)
CNKI学位论文(262)
知网期刊论文(82)
在“
Elsevier电子期刊
”中,
命中:
215
条,耗时:小于0.01 秒
在所有数据库中总计命中:
345
条
1.
Mitochondrial defects arise from nucleoside/nucleotide reverse transcriptase inhibitors in neurons: Potential contribution to HIV-associated neurocognitive disorders
作者:
Kui-Ming Hung
a
;
b
;
Pei-Chun Chen
b
;
Han-Chieh Hsieh
c
;
Marcus J Calkins
a
;
mjcalkins@mail.ncku.edu.tw
关键词:
NRTI
;
nucleoside/nucleotide reverse transcriptase inhibitor
;
HAND
;
HIV-associated neurocognitive disorders
;
cART
;
combination antiretroviral therapy
;
pol γ
;
polymerase γ
;
mtDNA
;
mitochondrial DNA
;
ddI
;
didanosine
;
AZT
;
zidovudine
;
FTC
;
emtricitabine
;
TDF
;
tenofovir
;
ddC
;
zalcitabine
;
d4T
;
stavudine
;
3TC
;
lamivudine
;
ABC
;
abacavir
;
PGC-1α
;
peroxisome proliferator-activated receptor γ coactivator 1α
;
mtUPR
;
mitochondrial unfolded protein response
;
CO1
;
Cytochrome oxidase I
;
ND1
;
NADH Dehydrogenase
刊名:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
出版年:2017
2.
Mutations in TFAM, encoding mitochondrial transcription factor A, cause neonatal liver failure associated with
mtDNA
depletion
作者:
Ashlee R. Stiles
a
;
b
;
1
;
Mariella T. Simon
c
;
d
;
1
;
Alexander Stover
c
;
Shaya Eftekharian
c
;
Negar Khanlou
a
;
Hanlin L. Wang
a
;
Shino Magaki
a
;
Hane Lee
a
;
b
;
Kate Partynski
c
;
Nagmeh Dorrani
e
;
Richard Chang
c
;
Julian A. Martinez-Agosto
b
;
e
;
f
;
Jose E. Abdenur
c
;
g
;
jabdenur@choc.org" class="auth_mail" title="E-mail the corresponding author
关键词:
TFAM mutation
;
mtDNA
depletion
syndrome
;
Liver failure
;
Newborn screening
;
Mitochondrial disease
刊名:Molecular Genetics and Metabolism
出版年:2016
3.
A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA
depletion
syndrome 13
作者:
Tuva Barø
;
y
a
;
1
;
tuva.baroy@medisin.uio.no" class="auth_mail" title="E-mail the corresponding author
;
Christeen Ramane J. Pedurupillay
a
;
1
;
p.j.c.ramane@medisin.uio.no" class="auth_mail" title="E-mail the corresponding author
;
Yngve T. Bliksrud
b
;
ybliksru@ous-hf.no" class="auth_mail" title="E-mail the corresponding author
;
Magnhild Rasmussen
c
;
marasmus@ous-hf.no" class="auth_mail" title="E-mail the corresponding author
;
Asbjø
;
rn Holmgren
a
;
asbjorh@student.matnat.uio.no" class="auth_mail" title="E-mail the corresponding author
;
Magnus D. Vigeland
a
;
magnusdv@medisin.uio.no" class="auth_mail" title="E-mail the corresponding author
;
Timothy Hughes
a
;
timothy.hughes@medisin.uio.no" class="auth_mail" title="E-mail the corresponding author
;
Maaike Brink
d
;
Maaike.Brink@radboudumc.nl" class="auth_mail" title="E-mail the corresponding author
;
Richard Rodenburg
d
;
Richard.Rodenburg@radboudumc.nl" class="auth_mail" title="E-mail the corresponding author
;
Bå
;
rd Nedregaard
e
;
bnedrega@ous-hf.no" class="auth_mail" title="E-mail the corresponding author
;
Petter Strø
;
mme
c
;
petter.stromme@medisin.uio.no" class="auth_mail" title="E-mail the corresponding author
;
Eirik Frengen
a
;
eirik.frengen@medisin.uio.no" class="auth_mail" title="E-mail the corresponding author
;
Doriana Misceo
a
;
doriana.misceo@medisin.uio.no" class="auth_mail" title="E-mail the corresponding author
关键词:
FBXL4
;
c.1442T>
C ;
p.Leu481Pro
;
Mitochondrial disorder
;
mtDNA
depletion
;
MTDPS13
刊名:European Journal of Medical Genetics
出版年:2016
4.
Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA
depletion
in a case of mitochondrial aconitase deficiency
作者:
Roa Sadat
a
;
Emanuele Barca
c
;
d
;
Ruchi Masand
b
;
Taraka R. Donti
b
;
Ali Naini
d
;
Darryl C. De Vivo
e
;
Salvatore DiMauro
d
;
Neil A. Hanchard
a
;
b
;
Brett H. Graham
b
;
bgraham@bcm.edu" class="auth_mail" title="E-mail the corresponding author
关键词:
Whole exome sequencing
;
mtDNA
depletion
;
Neurodegenerative disease
;
TCA cycle
;
Mitochondrial aconitase deficiency
刊名:Molecular Genetics and Metabolism
出版年:2016
5.
Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA
depletion
作者:
Hemant Varma
a
;
e
;
Phyllis L. Faust
a
;
Alejandro D. Iglesias
b
;
Stephen M. Lagana
a
;
Karen Wou
c
;
Michio Hirano
d
;
Salvatore DiMauro
d
;
Mahesh M. Mansukani
a
;
e
;
Kirsten E. Hoff
f
;
Peter L. Nagy
a
;
e
;
William C. Copeland
f
;
copelan1@niehs.nih.gov" class="auth_mail" title="E-mail the corresponding author
;
Ali B. Naini
a
;
e
;
abn2@cumc.columbia.edu" class="auth_mail" title="E-mail the corresponding author
关键词:
Mitochondrial DNA
depletion
;
POLG2
;
Hepatic failure
;
Whole-exome sequencing
;
POLG
刊名:European Journal of Medical Genetics
出版年:2016
6.
Potentially diagnostic electron paramagnetic resonance spectra elucidate the underlying mechanism of mitochondrial dysfunction in the deoxyguanosine kinase deficient rat model of a genetic mitochondrial DNA
depletion
syndrome
作者:
Brian Bennett
a
;
1
;
brian.bennett@mu.edu" class="auth_mail" title="E-mail the corresponding author
;
Daniel Helbling
b
;
dhelbling@mcw.edu" class="auth_mail" title="E-mail the corresponding author
;
Hui Meng
c
;
hmeng@mcw.edu" class="auth_mail" title="E-mail the corresponding author
;
Jason Jarzembowski
c
;
jjarzemb@mcw.edu" class="auth_mail" title="E-mail the corresponding author
;
Aron M. Geurts
d
;
ageurts@mcw.edu" class="auth_mail" title="E-mail the corresponding author
;
Marisa W. Friederich
e
;
Marisa.Friederich@ucdenver.edu" class="auth_mail" title="E-mail the corresponding author
;
Johan L.K. Van Hove
e
;
johan.vanhove@childrenscolorado.org" class="auth_mail" title="E-mail the corresponding author
;
Michael W. Lawlor
c
;
mlawlor@mcw.edu" class="auth_mail" title="E-mail the corresponding author
;
David P. Dimmock
b
;
ddimmock@mcw.edu" class="auth_mail" title="E-mail the corresponding author
关键词:
COX
;
cytochrome oxidase
;
M2
;
deoxyguanosine kinase-deficient rat model
;
DGUOK
;
deoxyguanosine kinase
;
EPR (ESR)
;
electron paramagnetic (spin) resonance (spectroscopy)
;
FeS
;
iron&ndash
;
sulfur (cluster)
;
H&E
;
hematoxylin and eosin
;
MD
;
mitochondrial disease
;
MDS
;
mitochondrial DNA
depletion
syndrome
;
MPV17
;
mitochondrial inner membrane protein
;
mtDNA
;
mitochondrial DNA
;
NADH
;
reduced nicotinamide adenine dinucleotide
;
POLG
;
DNA polymerase γ
;
SDH
;
succinate dehydrogenase
;
TWINKLE
;
a mitochondrial D
刊名:Free Radical Biology and Medicine
出版年:2016
7.
Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure
作者:
Annalinda Pisano
a
;
Bruna Cerbelli
a
;
Elena Perli
a
;
Maria Pelullo
b
;
Valentina Bargelli
c
;
Carmela Preziuso
a
;
Massimiliano Mancini
a
;
b
;
Langping He
d
;
Matthew GD Bates
d
;
Joaquin R Lucena
e
;
Paola Lilla Della Monica
f
;
Giuseppe Familiari
g
;
Vincenzo Petrozza
h
;
Chiara Nediani
c
;
Robert W Taylor
d
;
Giulia d&rsquo
;
Amati
a
;
Carla Giordano
a
;
carla.giordano@uniroma1.it" class="auth_mail" title="E-mail the corresponding author
关键词:
HF
;
heart failure
;
LV
;
left ventricular
;
OXPHOS
;
oxidative phosphorylation
;
mtDNA
;
mitochondrial DNA
;
MIC
;
mitochondrial cardiomyopathies
;
LCM
;
laser capture microdissection
;
COX
;
cytochrome c oxidase
;
SDH
;
succinate dehydrogenase
;
TEM
;
transmission electron microscopy
;
PPARα
;
peroxisome proliferator-activated receptor alpha PPARA
;
PGC-1α
;
peroxisome proliferator-activated receptor gamma coactivator 1 alpha
;
PPARGC1A
;
NPPA
;
natriuretic peptide A
;
NRF1
;
nuclear respiratory factor 1
;
ERRα
;
estroge
刊名:Cardiovascular Pathology
出版年:2016
8.
Effects of reduced mitochondrial DNA content on secondary mitochondrial toxicant exposure in Caenorhabditis elegans
作者:
Anthony L. Luz
anthony.luz@duke.edu" class="auth_mail" title="E-mail the corresponding author
;
Joel N. Meyer
;
joel.meyer@duke.edu" class="auth_mail" title="E-mail the corresponding author
关键词:
mtDNA
depletion
;
Caenorhabditis elegans
;
DNA damage
;
Ultraviolet C
;
Arsenite
;
Environmental toxicant
刊名:Mitochondrion
出版年:2016
9.
Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria
作者:
Yupeng Liu
;
Xiyuan Li
;
Qiao Wang
;
Yuan Ding
;
Jinqing Song
;
Yanling Yang
;
organic.acid@126.com" class="auth_mail" title="E-mail the corresponding author
;
yanlingy@vip.sina.com" class="auth_mail" title="E-mail the corresponding author
关键词:
Methylmalonic aciduria
;
Succinate-CoA ligase deficiency
;
Encephalomyopathy
;
Mitochondrial DNA
depletion
;
SUCLG1
刊名:Brain and Development
出版年:2016
10.
Lack of mitochondrial DNA impairs chemical hypoxia-induced autophagy in liver tumor cells through ROS-AMPK-ULK1 signaling dysregulation independently of HIF-1α
作者:
Jose J.G. Marin
a
;
Elisa Lozano
a
;
Maria J. Perez
a
;
b
;
mjperez@usal.es
关键词:
Akt
;
protein kinase B
;
AMPK
;
AMP-activated protein kinase
;
AVOs
;
acidic vesicular organelles
;
BNIP3
;
BCL2/adenovirus E1B 19
;
kDa interacting protein 3
;
BNIP3L
;
BCL2/adenovirus E1B 19
;
kDa interacting protein 3-like
;
CCND1
;
cyclin D1
;
CFSE
;
5-(6)-carboxyfluorescein diacetate succinimidyl ester
;
CQ
;
chloroquine
;
CHOP
;
C/EBP homologous protein
;
CoCl2
;
cobalt chloride
;
DCFH-DA
;
2&prime
;
7&prime
;
-dichlorofluorescein diacetate
;
DFO
;
deferoxamine
;
ER
;
endoplasmic reticulum
;
ERK
;
extracellular r
刊名:Free Radical Biology and Medicine
出版年:2016
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