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Elsevier电子期刊(7)
在“
Elsevier电子期刊
”中,
命中:
7
条,耗时:小于0.01 秒
在所有数据库中总计命中:
7
条
1.
Contribution of PTPN22, CD28, CTLA-4 and ZAP-70 variants to the risk of type 1 diabetes in Tunisians
作者:
Ferjeni Zouidi
;
Mouna Stayoussef
;
Dorra Bouzid
;
Hajer Fourati
;
Olfa Abida
;
M. Ben Ayed
;
Thouraya
Kammoun
;
Monjia Hachicha
;
Carlos Penha-Gon莽alves
;
Hatem Masmoudi
关键词:
T1D
;
Type 1 diabetes
;
HWE
;
Hardy&ndash
;
Weinberg equilibrium
;
OR
;
odds ratios
;
LD
;
linkage disequilibrium
;
haplotype
刊名:Gene
出版年:1 January, 2014
2.
Association of BANK1 and cytokine gene polymorphisms with type 1 diabetes in Tunisia
作者:
Ferjani Zouidi
;
Mouna Stayoussef
;
Dorra Bouzid
;
Hajer Fourati
;
Olfa Abida
;
Costa Jo茫o
;
Mourad Ben Ayed
;
Raouia Fakhfakh
;
Kammoun
Thouraya
;
Hachicha Monjia
;
Penha-Gon莽alves Carlos
;
Hatem Masmoudi
关键词:
T1D
;
type 1 diabetes
;
AID
;
autoimmune disease
;
BANK1
;
B-cell scaffold protein with ankyrin repeats 1
;
SLE
;
systemic lupus erythematosus
;
SSc
;
systemic sclerosis
;
RA
;
rheumatoid arthritis
;
HWE
;
Hardy&ndash
;
Weinberg equilibrium
;
OR
;
odds ratios
;
LD
;
linkage disequilibrium
刊名:Gene
出版年:25 February, 2014
3.
Dietary intakes of essential nutrients among Arab and Berber ethnic groups on rural Tunisian island
作者:
Thouraya
Baroudi
;
Hedi Ben Maiz
;
Hafaoua
Kammoun
Abid
;
Amel Benammar-Elgaaied
;
Leila Trabelsi Alouane
关键词:
Ethnicity
;
Dietary intake
;
Arabs
;
Berbers
;
Jerba Island
刊名:Nutrition
出版年:2010
4.
A case of Kearns–Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles
作者:
Emna Mkaouar-Rebai
;
Imen Chamkha
;
Thouraya
Kammoun
;
Imen Chabchoub
;
Hajer Aloulou
;
Nourhene Fendri
;
Mongia Hachicha
;
Faiza Fakhfakh
关键词:
Kearns–
;
Sayre syndrome
;
mtDNA deletion
;
Mitochondrial DNA
;
Heteroplasmy
;
Long-range PCR
;
Common deletion
刊名:Mitochondrion
出版年:2010
5.
Two new mutations in the MT-TW gene leading to the disruption of the secondary structure of the tRNA
Trp
in patients with Leigh syndrome
作者:
Emna Mkaouar-Rebai
;
Imen Chamkha
;
Fatma
Kammoun
;
Thouraya
Kammoun
;
Hajer Aloulou
;
Mongia Hachicha
;
Chahnez Triki
;
Faiza Fakhfakh
关键词:
Leigh syndrome
;
Mitochondrial mutations
;
Mitochondrial polymorphisms
;
MT-TW
刊名:Molecular Genetics and Metabolism
出版年:2009
6.
The G1057D polymorphism of IRS-2 gene is not associated with type 2 diabetes and obese patients among ethnic groups in Tunisian population
作者:
Thouraya
Baroudi Ouederni
;
Jose Sanchez-Corona
;
Silvia E. Flores Martinez
;
Hedi Ben Maiz
;
Hajer Aounallah Skhiri
;
Hafaoua
Kammoun
Abid
;
Amel Benammar-Elgaaied
关键词:
Insulin receptor substrate 2
;
Gly1057Asp variant
;
Type 2 diabetes
;
Ethnicity
;
Djerba Island
刊名:Clinical Biochemistry
出版年:2009
7.
Vascularite avec atteinte rénale et anticorps anticytoplasme des polynucléaires neutrophiles (ANCA) après prise de benzylthio-uracile chez l'enfant
作者:
Mongia Hachicha
;
Thouraya
Kammoun
;
Wafa Ben Romdhane
;
Rim Ben Abdallah
;
Abdelmajid Mahfoudh
;
Khaoula
Kammoun
;
Jamil Hachicha
;
Ali Triki
关键词:
Grave's disease
;
Vasculitis
;
Glomerulonephritis
;
ANCA
;
Benzylthiouracil
;
Child
刊名:Néphrologie & Thérapeutique
出版年:2007
1
按检索点细分(7)
作者(7)
按出版年细分(7)
2027年及以后(1)
2010年(2)
2009年(2)
2007年(1)
2000年及以前(1)
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