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Wiley电子期刊(1)
SpringerLink电子期刊(4)
Elsevier电子期刊(12)
在“
Elsevier电子期刊
”中,
命中:
12
条,耗时:0.0219892 秒
在所有数据库中总计命中:
17
条
1.
A novel TECTA mutation causes ARNSHL
作者:
Samira Asgharzade
a
;
e
;
Mohammad
Amin
Tabatabaie
far
b
;
Mohammad
Hossein Modarressi
a
;
Mohammad
Hossein Ghahremani
a
;
Somayeh Reiisi
c
;
Parisa Tahmasebi
d
;
Fatemeh Abdollahnejad
d
;
Morteza Hashemzadeh Chaleshtori
e
;
mchalesh@yahoo.com
关键词:
TECTA
;
Hearing loss
;
Linkage analysis
;
Mutation
;
Iran
刊名:International Journal of Pediatric Otorhinolaryngology
出版年:2017
2.
Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations
作者:
Nazanin Jalilian
a
;
Mohammad
Amin
Tabatabaie
far
b
;
c
;
Mohammad
Farhadi
d
;
Tayeb Bahrami
a
;
Hesam Emamdjomeh
d
;
Mohammad
Reza Noori-Daloii
a
;
nooridaloii@tums.ac.ir" class="auth_mail" title="E-mail the corresponding author
关键词:
DC
;
dystopia canthorum
;
HL
;
hearing loss
;
EDTA
;
ethylenedi
amin
etetraacetic acid
;
WS
;
Waardenburg syndrome
;
PCR
;
polymerase chain reaction
;
STR
;
short tandem repeat
刊名:Gene
出版年:2015
3.
A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family
作者:
Nazanin Jalilian
a
;
Mohammad
Amin
Tabatabaie
far
b
;
c
;
Mohammad
Farhadi
d
;
Tayyeb Bahrami
a
;
Mohammad
Reza Noori-Daloii
a
;
nooridaloii@tums.ac.ir" class="auth_mail" title="E-mail the corresponding author
关键词:
Waardenburg syndrome type 1
;
PAX3
;
Novel mutation
;
Iran
刊名:International Journal of Pediatric Otorhinolaryngology
出版年:2015
4.
Association of interleukin-1 gene cluster polymorphisms and haplotypes with multiple sclerosis in an Iranian population
作者:
Ayyoob Khosravi
a
;
Bita Javan
a
;
Mohammad
Amin
Tabatabaie
far
b
;
Hamid Ebadi
a
;
c
;
Davood Fathi
a
;
c
;
Majid Shahbazi
a
;
shahbazimajid@yahoo.co.uk" class="auth_mail" title="E-mail the corresponding author
关键词:
Multiple sclerosis
;
Interleukin-1
;
Genetic susceptibility
;
Haplotype
刊名:Journal of Neuroimmunology
出版年:2015
5.
Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: Assessment of GJB4, GJA1, and GJC3
作者:
Daniz Kooshavar
a
;
b
;
dkooshavar@razi.tums.ac.ir
;
Mohammad
Amin
Tabatabaie
far
b
;
c
;
tabatabaie
far@gmail.com
;
Effat Farrokhi
b
;
Marziye Abolhasani
b
;
Mohammad
-Reza Noori-Daloii
a
;
nooridaloii@sina.tums.ac.ir
;
Morteza Hashemzadeh-Chaleshtori
b
;
mchalesh@skums.ac.ir
;
mchalesh@yahoo.com
关键词:
Cx
;
connexin
;
GJ
;
gap junction
;
HL
;
hearing loss
;
ARNSHL
;
autosomal recessive non-syndromic hearing loss
刊名:International Journal of Pediatric Otorhinolaryngology
出版年:2013
6.
Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms
作者:
Maryam Sobhani
;
Mohammad
Amin
Tabatabaie
far
;
Asadollah Rajab
;
Abdol-
Mohammad
Kajbafzadeh
;
Mohammad
Reza Noori-Daloii
关键词:
WS
;
Wolfram syndrome
;
STR
;
short tandem repeats
;
DNA
;
deoxyribonucleic acid
;
Dup
;
duplication
;
DM
;
diabetes mellitus
;
DI
;
diabetes insipidus
;
OA
;
optic atrophy
;
DI-DM-OA-D
;
diabetes insipidus
;
diabetes mellitus
;
optic atrophy and deafness
;
FVC
;
frequency
刊名:Gene
出版年:2013
7.
A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect
作者:
Elham Davoudi-Dehaghani
a
;
b
;
Sirous Zeinali
a
;
c
;
zeinali@kawsar.ir
;
SirusZeinali@yahoo.com
;
Nejat Mahdieh
c
;
d
;
Atefeh Shirkavand
e
;
Hamideh Bagherian
c
;
Mohammad
Amin
Tabatabaie
far
f
关键词:
TMC1
;
DFNB7/11
;
Mutation
;
Autosomal recessive non-syndromic hearing loss
;
Iran
;
Ethnicity
刊名:International Journal of Pediatric Otorhinolaryngology
出版年:2013
8.
Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss
作者:
Nasrin Yazdanpanahi
a
;
nasrin232002@yahoo.com
;
Morteza Hashemzadeh Chaleshtori
b
;
Mohammad
Amin
Tabatabaie
far
b
;
c
;
Zahra Noor
mohammad
i
a
;
Effat Farrokhi
b
;
Hossein Najmabadi
d
;
Shirin Shahbazi
b
;
Azam Hosseinipour
b
关键词:
Novel mutation
;
Pendrin
;
Slc26a4
;
Pendred syndrome (PS)
;
Deafness
;
Linkage analysis
;
Iran
刊名:International Journal of Pediatric Otorhinolaryngology
出版年:2012
9.
A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment
作者:
Isabelle Schrauwen
;
Sarah Helfmann
;
Akira Inagaki
;
Friederike Predoehl
;
Mohammad
?
Amin
Tabatabaie
far
;
Maria?Magdalena Picher
;
Manou Sommen
;
Celia?Zazo Seco
;
Jaap Oostrik
;
Hannie Kremer
;
Annelies Dheedene
;
Charlotte Claes
;
Erik Fransen
;
Morteza?Hashemzadeh Chaleshtori
;
Paul Coucke
;
Amy Lee
;
Tobias Moser
;
Guy Van?Camp
刊名:The American Journal of Human Genetics
出版年:2012
10.
A synthetic macromolecule as MRI detectable drug carriers:
Amin
odextran-coated iron oxide nanoparticles
作者:
Mohammad
Reza Saboktakin
;
Roya M.
Tabatabaie
;
Abel Maharramov
;
Mohammad
Ali Ramazanov
关键词:
Macromolecule
;
MRI
;
Amin
odextran
;
Iron oxide nanoparticles
;
Drug carriers
刊名:Carbohydrate Polymers
出版年:2010
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