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Pregled bibliografske jedinice broj: 133477

The role of D6S265, D6S273, and MIB polymorphisms in development of IDDM


Štingl, Katarina; Grubić, Zorana; Žunec, Renata; Čečuk-Jeličić, Esma; Radica, Ana; Dumić, Miroslav; Brkljačić-Kerhin, Vesna
The role of D6S265, D6S273, and MIB polymorphisms in development of IDDM // Genes and Immunity, 4 (2003), 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)


CROSBI ID: 133477 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
The role of D6S265, D6S273, and MIB polymorphisms in development of IDDM

Autori
Štingl, Katarina ; Grubić, Zorana ; Žunec, Renata ; Čečuk-Jeličić, Esma ; Radica, Ana ; Dumić, Miroslav ; Brkljačić-Kerhin, Vesna

Izvornik
Genes and Immunity (1466-4879) 4 (2003), 1;

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, kongresno priopcenje, znanstveni

Ključne riječi
D6S265; D6S273; MIB; IDDM

Sažetak
Recent investigations have indicated the existence of non-HLA loci associated with IDDM in addition to HLA class II genes. One hundred patients selected on the basis of their HLA class II alleles, where classified in 4 groups (DR3/DR4, DR3, DR4, non DR3/DR4). PCR-SSP method was performed for HLA class II typing, while 3 microsatellites (D6S265, D6S273, and MIB) were analysed using automated ALF express sequencer. The frequency of D6S273 126bp (p=0.02565), 138bp (p=0.01967) and 140bp (p=0.00035) were significantly higher among patients, while the frequency of D6S273 130bp was significantly lower. Analysis of the MIB alleles revealed an increased frequency of alleles 348bp (p=0.01302), 350bp (p=0.00677) and 352bp (p=0.02289) among IDDM, while allele 334bp (p=0.00105) was decreased. There was no difference between patients and controls at D6S265 locus. Comparison of 3 IDDM groups positive for DRB1*0301/*04 with non DRB1*03/*04 patients was also performed, and allele 132bp was present with a significantly higher frequency (p=0.00283) among DRB1*0301/*04 negative patients. This suggests that all other D6S273 and MIB alleles showed association with IDDM because of linkage disequilibrium with DRB1 alleles. When non DRB1*03/*04 group was compared with matched controls, difference in frequency of 132bp allele was also significant (p=0.03986). Our results lead to conclusion that allele 273bp has an independent role in development of IDDM.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Projekti:
0108123

Ustanove:
Medicinski fakultet, Zagreb


Citiraj ovu publikaciju:

Štingl, Katarina; Grubić, Zorana; Žunec, Renata; Čečuk-Jeličić, Esma; Radica, Ana; Dumić, Miroslav; Brkljačić-Kerhin, Vesna
The role of D6S265, D6S273, and MIB polymorphisms in development of IDDM // Genes and Immunity, 4 (2003), 1. (podatak o recenziji nije dostupan, kongresno priopcenje, znanstveni)
Štingl, K., Grubić, Z., Žunec, R., Čečuk-Jeličić, E., Radica, A., Dumić, M. & Brkljačić-Kerhin, V. (2003) The role of D6S265, D6S273, and MIB polymorphisms in development of IDDM. Genes and Immunity, 4 (1).
@article{article, author = {\v{S}tingl, Katarina and Grubi\'{c}, Zorana and \v{Z}unec, Renata and \v{C}e\v{c}uk-Jeli\v{c}i\'{c}, Esma and Radica, Ana and Dumi\'{c}, Miroslav and Brklja\v{c}i\'{c}-Kerhin, Vesna}, year = {2003}, pages = {S38}, keywords = {D6S265, D6S273, MIB, IDDM}, journal = {Genes and Immunity}, volume = {4}, number = {1}, issn = {1466-4879}, title = {The role of D6S265, D6S273, and MIB polymorphisms in development of IDDM}, keyword = {D6S265, D6S273, MIB, IDDM} }
@article{article, author = {\v{S}tingl, Katarina and Grubi\'{c}, Zorana and \v{Z}unec, Renata and \v{C}e\v{c}uk-Jeli\v{c}i\'{c}, Esma and Radica, Ana and Dumi\'{c}, Miroslav and Brklja\v{c}i\'{c}-Kerhin, Vesna}, year = {2003}, pages = {S38}, keywords = {D6S265, D6S273, MIB, IDDM}, journal = {Genes and Immunity}, volume = {4}, number = {1}, issn = {1466-4879}, title = {The role of D6S265, D6S273, and MIB polymorphisms in development of IDDM}, keyword = {D6S265, D6S273, MIB, IDDM} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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