Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Naci, Degerli"'
Publikováno v:
Genetics and Molecular Biology, Vol 27, Iss 2, Pp 162-164 (2004)
NAT1 is an intronless gene on chromosome 8p21.3 encoding a 290-amino-acid-long protein showing acetyltransferase activity. Some 26 alleles of NAT1 gene have been identified in human populations. In the present study we determined the distributions of
Externí odkaz:
https://doaj.org/article/b415113daaf040fa879bc1fbf85e8678
Publikováno v:
Journal of Biogeography. 41:1793-1805
WOS: 000342055900015
Aim Chorthippus parallelus is one of the classic model systems for studying genetic structure and phylogeography in the Western Palaearctic. Here, we investigate the regional genetic differentiation of C. parallelus and eval
Aim Chorthippus parallelus is one of the classic model systems for studying genetic structure and phylogeography in the Western Palaearctic. Here, we investigate the regional genetic differentiation of C. parallelus and eval
Autor:
SevgiDurna, Dastan, Naci, Degerli, Taner, Dastan, Fazilet, Yildiz, Yavuz, Yildir, Yusuf Muhammed, Durna, Dilek, Atessahin, Tunay, Karan
Publikováno v:
Pakistan journal of pharmaceutical sciences. 28
Ability to taste Phenylthiocarbamide (PTC) a bitter molecule, is usually used to know the heritable characteristic in both genetic and physiological studies. So far, no research has yet attested whether PTC blindness relation with obesity and some nu
Publikováno v:
Current Medical Research and Opinion. 20:533-540
WOS: 000220994200014
PubMed ID: 15119991
Objective: Constitutive activation of various hormone and growth factor receptors is newly recognised as a common cause of tumour development. This study investigated the presence of any mutation or
PubMed ID: 15119991
Objective: Constitutive activation of various hormone and growth factor receptors is newly recognised as a common cause of tumour development. This study investigated the presence of any mutation or
Publikováno v:
Journal of Cellular and Molecular Medicine. 7:307-312
WOS: 000224538000012
PubMed ID: 14594555
This paper aimed to analyze the association of polymorphism of GSTM1 0/0 genotype with laryngeal cancer along a hospital based case-control study. Polymorphisms of GSTM 1 0/0 of samples from 36 patie
PubMed ID: 14594555
This paper aimed to analyze the association of polymorphism of GSTM1 0/0 genotype with laryngeal cancer along a hospital based case-control study. Polymorphisms of GSTM 1 0/0 of samples from 36 patie
Publikováno v:
Turkish Journal of Fisheries and Aquatic Sciences. 12
In this study, the phylogenetic and phylogeographic relationships among Cyprinion macrostomus HECKEL, 1843, Cyprinion kais HECKEL, 1843 and Carasobarbus chantrei SAUVAGE, 1882 samples from Anatolia was analysed. While doing this, mitochondrial DNA po
WOS: 000275581200009
In the present study, mitochondrial DNA polymerase chain reaction-restriction-fragment length polymorphism (PCR-RFLP) and nuclear DNA inter-simple sequence repeat (ISSR) assays were used to assess the phylogenetic and phylog
In the present study, mitochondrial DNA polymerase chain reaction-restriction-fragment length polymorphism (PCR-RFLP) and nuclear DNA inter-simple sequence repeat (ISSR) assays were used to assess the phylogenetic and phylog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::904320566e135e679c78b4bfda834d01
https://hdl.handle.net/20.500.12418/9930
https://hdl.handle.net/20.500.12418/9930
WOS: 000235983000004
In the present study, mitochondrial DNA polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay was used to assess the phylogenetic and phylogeographic relationships among 27 brown trout Salmo tru
In the present study, mitochondrial DNA polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay was used to assess the phylogenetic and phylogeographic relationships among 27 brown trout Salmo tru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40c74a62a789f94ad8ed26873bba5d27
https://hdl.handle.net/20.500.12418/10867
https://hdl.handle.net/20.500.12418/10867
Publikováno v:
Clinical biochemistry. 38(3)
WOS: 000227206700008
PubMed ID: 15708547
Objective: In the present study, we determined the frequency of Delta32 allele distribution and its relationship with various carcinomas in a Turkish population. Design and methods: We determined the
PubMed ID: 15708547
Objective: In the present study, we determined the frequency of Delta32 allele distribution and its relationship with various carcinomas in a Turkish population. Design and methods: We determined the
Publikováno v:
Genetics and Molecular Biology v.27 n.2 2004
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 27, Issue: 2, Pages: 162-164, Published: 2004
Genetics and Molecular Biology, Vol 27, Iss 2, Pp 162-164 (2004)
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 27, Issue: 2, Pages: 162-164, Published: 2004
Genetics and Molecular Biology, Vol 27, Iss 2, Pp 162-164 (2004)
WOS: 000222989100005
NAT1 is an intronless gene on chromosome 8p21.3 encoding a 290-amino-acid-long protein showing acetyltransferase activity. Some 26 alleles of NAT1 gene have been identified in human populations. In the present study we deter
NAT1 is an intronless gene on chromosome 8p21.3 encoding a 290-amino-acid-long protein showing acetyltransferase activity. Some 26 alleles of NAT1 gene have been identified in human populations. In the present study we deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c141d55f78439aeb732d3e0a1f733c8
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572004000200005
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572004000200005