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BM Sürdürülebilir Kalkınma Amaçları
Raporlar ve İstatistikler
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Giriş
Yayın Arama
Prof. Dr.
Doç. Dr.
Dr. Öğr. Üyesi
Öğr. Gör.
Arş. Gör.
Diğer
Toplam 27651 kayıt
The association between endothelial nitric oxide synthase gene Glu298Asp polymorphism and spontaneous pregnancy loss
Yalcıntepe, S.,
ÖZDEMİR, Ö.
, Hacıvelioğlu, O., Akurut, C., Kumcular, T., Uysal, D., Yucesoy, K., Uludağ, A., Cosar, E., Sılan, F. () "
The association between endothelial nitric oxide synthase gene Glu298Asp polymorphism and spontaneous pregnancy loss
",
European Human Genetics Conference (ESHG)
Yalcıntepe, S.,
ÖZDEMİR, Ö.
, Hacıvelioğlu, O., Akurut, C., Kumcular, T., Uysal, D., Yucesoy, K., Uludağ, A., Cosar, E., Sılan, F. () "
The association between endothelial nitric oxide synthase gene Glu298Asp polymorphism and spontaneous pregnancy loss
",
European Human Genetics Conference (ESHG)
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics Conference (ESHG)
Variable R Msp1 fragmentation in genomic DNA due to DNA hypomethylation in CRF patients with MTHFR C677Tgene polymorphism from genetics to epigenetics
ÖZDEMİR, Ö.
, Urfalı, M., Sılan, F., Uludağ, A., Arı, E., Kayatas, M. () "
Variable R Msp1 fragmentation in genomic DNA due to DNA hypomethylation in CRF patients with MTHFR C677Tgene polymorphism from genetics to epigenetics
",
European Human Genetics Conference (ESHG)
ÖZDEMİR, Ö.
, Urfalı, M., Sılan, F., Uludağ, A., Arı, E., Kayatas, M. () "
Variable R Msp1 fragmentation in genomic DNA due to DNA hypomethylation in CRF patients with MTHFR C677Tgene polymorphism from genetics to epigenetics
",
European Human Genetics Conference (ESHG)
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics Conference (ESHG)
High frequency of chromosomal anomalies and a novelchromosomal insertion associated with infertility and recurrent miscarriages Reproductive Failure in west Turkey
Sılan, F., Yalcıntepe, S., Uysal, D., Urfalı, M., Uludağ, A.,
ÖZDEMİR, Ö.
, Sık, E., Cosar, E., Cakır, A. () "
High frequency of chromosomal anomalies and a novelchromosomal insertion associated with infertility and recurrent miscarriages Reproductive Failure in west Turkey
",
European Human Genetics Conference (ESHG)
Sılan, F., Yalcıntepe, S., Uysal, D., Urfalı, M., Uludağ, A.,
ÖZDEMİR, Ö.
, Sık, E., Cosar, E., Cakır, A. () "
High frequency of chromosomal anomalies and a novelchromosomal insertion associated with infertility and recurrent miscarriages Reproductive Failure in west Turkey
",
European Human Genetics Conference (ESHG)
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics Conference (ESHG)
High frequency of chromosomal anomalies and a novelchromosomal insertion associated with infertility and recurrent miscarriages Reproductive Failure in west Turkey
Sılan, F., Yalcıntepe, S., Uysal, D., Urfalı, M., Uludağ, A.,
ÖZDEMİR, Ö.
, Sık, E., Cosar, E., Cakır, A. () "
High frequency of chromosomal anomalies and a novelchromosomal insertion associated with infertility and recurrent miscarriages Reproductive Failure in west Turkey
",
European Human Genetics Conference (ESHG)
Sılan, F., Yalcıntepe, S., Uysal, D., Urfalı, M., Uludağ, A.,
ÖZDEMİR, Ö.
, Sık, E., Cosar, E., Cakır, A. () "
High frequency of chromosomal anomalies and a novelchromosomal insertion associated with infertility and recurrent miscarriages Reproductive Failure in west Turkey
",
European Human Genetics Conference (ESHG)
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics Conference (ESHG)
Deleterious mutations in mitochondrial NADH dehydrogenase subunit 4 and ATPase subunit 6 in two siblings of Leigh Syndrome with progressive motor retardation and loss of visual function
Urfalı, M.,
ÖZDEMİR, Ö.
, Kankaya, D., Uludağ, A., Yalçıntepe, S., Sılan, F. () "
Deleterious mutations in mitochondrial NADH dehydrogenase subunit 4 and ATPase subunit 6 in two siblings of Leigh Syndrome with progressive motor retardation and loss of visual function
",
European Human Genetics Conference (ESHG)
Urfalı, M.,
ÖZDEMİR, Ö.
, Kankaya, D., Uludağ, A., Yalçıntepe, S., Sılan, F. () "
Deleterious mutations in mitochondrial NADH dehydrogenase subunit 4 and ATPase subunit 6 in two siblings of Leigh Syndrome with progressive motor retardation and loss of visual function
",
European Human Genetics Conference (ESHG)
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics Conference (ESHG)
Functional gene mediated oncogenesis by germ line MTHFR polymorphism in colorectal carcinoma
Ozen, F., Sen, M., Ozcırak, S., Çolak, A.,
ÖZDEMİR, Ö.
() "
Functional gene mediated oncogenesis by germ line MTHFR polymorphism in colorectal carcinoma
",
9th European Cytogenetics Conference
Ozen, F., Sen, M., Ozcırak, S., Çolak, A.,
ÖZDEMİR, Ö.
() "
Functional gene mediated oncogenesis by germ line MTHFR polymorphism in colorectal carcinoma
",
9th European Cytogenetics Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
9th European Cytogenetics Conference
Polymorphism in gene encoding drugs and xenobiotic metabolizing enzyme CYP2D6 as a risk factor for drug response in colchicine unresponsive FMF patients
Atik, S., Ozen, F., Gur, S., Uludağ, A., Sılan, C., Sılan, F.,
ÖZDEMİR, Ö.
() "
Polymorphism in gene encoding drugs and xenobiotic metabolizing enzyme CYP2D6 as a risk factor for drug response in colchicine unresponsive FMF patients
",
European Human Genetics Conference
Atik, S., Ozen, F., Gur, S., Uludağ, A., Sılan, C., Sılan, F.,
ÖZDEMİR, Ö.
() "
Polymorphism in gene encoding drugs and xenobiotic metabolizing enzyme CYP2D6 as a risk factor for drug response in colchicine unresponsive FMF patients
",
European Human Genetics Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics Conference
Tumoral tissue specific promoter hypermethylation of tumor supressor genes SFRp2 p16 DAPK1 HIC and MGMT in a case with non small cell carcinoma A case report
Arslan, S., Doğan, T., Koksal, B., Yıldırım, M., Gumus, C., Elagoz, C., Akkurt, I.,
ÖZDEMİR, Ö.
(2009) "
Tumoral tissue specific promoter hypermethylation of tumor supressor genes SFRp2 p16 DAPK1 HIC and MGMT in a case with non small cell carcinoma A case report
",
7th European Cytogenetics Conference
, (
Temmuz 2009
)
Arslan, S., Doğan, T., Koksal, B., Yıldırım, M., Gumus, C., Elagoz, C., Akkurt, I.,
ÖZDEMİR, Ö.
(2009) "
Tumoral tissue specific promoter hypermethylation of tumor supressor genes SFRp2 p16 DAPK1 HIC and MGMT in a case with non small cell carcinoma A case report
",
7th European Cytogenetics Conference
, (
Temmuz 2009
)
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
2009
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
7th European Cytogenetics Conference
Chromosome 7 duplication in a young girl with congenital heart disease unusual behaviours and low IQ level clinical and cytogenetical characterisation
Sezgin, İ., Çolak, A., Cakar, E., Ozen, F., Kocak, N., Ejder, M.,
ÖZDEMİR, Ö.
() "
Chromosome 7 duplication in a young girl with congenital heart disease unusual behaviours and low IQ level clinical and cytogenetical characterisation
",
European Human Genetics Conference
Sezgin, İ., Çolak, A., Cakar, E., Ozen, F., Kocak, N., Ejder, M.,
ÖZDEMİR, Ö.
() "
Chromosome 7 duplication in a young girl with congenital heart disease unusual behaviours and low IQ level clinical and cytogenetical characterisation
",
European Human Genetics Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics Conference
Homeobox gene Pax9 variation in a family with Hypohidrotic Ectodermal Dysplasia
O., O., A., C., G., B., M, A., R, G., E, G. () "
Homeobox gene Pax9 variation in a family with Hypohidrotic Ectodermal Dysplasia
",
European Human Genetics conference Amsterdam, The Netherlands
O., O., A., C., G., B., M, A., R, G., E, G. () "
Homeobox gene Pax9 variation in a family with Hypohidrotic Ectodermal Dysplasia
",
European Human Genetics conference Amsterdam, The Netherlands
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics conference Amsterdam, The Netherlands
In Vivo Evaluation Of Micronuclei In Rat Reticulocytes For The Relative Efficacy Of Genomic Instability In Medical Radiation Exposure
H., E., E., G., T., E., C, G.,
O, O.S.A.O.
() "
In Vivo Evaluation Of Micronuclei In Rat Reticulocytes For The Relative Efficacy Of Genomic Instability In Medical Radiation Exposure
",
5.th Euoropean Cytogenetics Conference
H., E., E., G., T., E., C, G.,
O, O.S.A.O.
() "
In Vivo Evaluation Of Micronuclei In Rat Reticulocytes For The Relative Efficacy Of Genomic Instability In Medical Radiation Exposure
",
5.th Euoropean Cytogenetics Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
5.th Euoropean Cytogenetics Conference
The SSCP profiles of mutated homeobox PAX9 gene in orofacial clefts in human Two cases report
ÖZDEMİR, Ö.
, Özdemir, A., Doruk, C., Gül, E., Yılmaz, S., Coskun, A., Bolayır, G., Kılıc, B., Ozdemir, D., Kılıc, B. () "
The SSCP profiles of mutated homeobox PAX9 gene in orofacial clefts in human Two cases report
",
5.th Euoropean Cytogenetics Conference
ÖZDEMİR, Ö.
, Özdemir, A., Doruk, C., Gül, E., Yılmaz, S., Coskun, A., Bolayır, G., Kılıc, B., Ozdemir, D., Kılıc, B. () "
The SSCP profiles of mutated homeobox PAX9 gene in orofacial clefts in human Two cases report
",
5.th Euoropean Cytogenetics Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
5.th Euoropean Cytogenetics Conference
Klomifen Sitratın rat kemikiliği kök hücrelerindeki genetik etkileri
B., D., Y., D., T., T., Ö, Ö., Y, T., M, Ç. () "
Klomifen Sitratın rat kemikiliği kök hücrelerindeki genetik etkileri
",
XI. TİVAK & I. Türk-Fransız Üreme Tıbbi ve İnfertilite Kongresi
B., D., Y., D., T., T., Ö, Ö., Y, T., M, Ç. () "
Klomifen Sitratın rat kemikiliği kök hücrelerindeki genetik etkileri
",
XI. TİVAK & I. Türk-Fransız Üreme Tıbbi ve İnfertilite Kongresi
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
XI. TİVAK & I. Türk-Fransız Üreme Tıbbi ve İnfertilite Kongresi
Comperative karyometric study of rhinosinus polyposisand normal nasal mucosa
A., Y., Ö., Ö., E., G., B, Y., S, K., T, K. () "
Comperative karyometric study of rhinosinus polyposisand normal nasal mucosa
",
20 th Congress of the European Rhinologic Society and 23 rd International Symposium on infection and allergy of the nose
A., Y., Ö., Ö., E., G., B, Y., S, K., T, K. () "
Comperative karyometric study of rhinosinus polyposisand normal nasal mucosa
",
20 th Congress of the European Rhinologic Society and 23 rd International Symposium on infection and allergy of the nose
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
20 th Congress of the European Rhinologic Society and 23 rd International Symposium on infection and allergy of the nose
Proto oncogene c myc SSCP prifiles in human bladder urothelial carcinoma tissues
E., Y., O., O., S., A., E, G. () "
Proto oncogene c myc SSCP prifiles in human bladder urothelial carcinoma tissues
",
European Human Genetics Conference
E., Y., O., O., S., A., E, G. () "
Proto oncogene c myc SSCP prifiles in human bladder urothelial carcinoma tissues
",
European Human Genetics Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Human Genetics Conference
Is your patient s problem just cleft lip and palate
C., D., F., P., O, S.O.A.O. () "
Is your patient s problem just cleft lip and palate
",
2nd World Cleft Congress
C., D., F., P., O, S.O.A.O. () "
Is your patient s problem just cleft lip and palate
",
2nd World Cleft Congress
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
2nd World Cleft Congress
Acut effect of I 131 treatment on chromosomes
T., E., S., S., S., Ö., D, O., Ö, Ö. () "
Acut effect of I 131 treatment on chromosomes
",
European Journal of Nuclear Medicine
T., E., S., S., S., Ö., D, O., Ö, Ö. () "
Acut effect of I 131 treatment on chromosomes
",
European Journal of Nuclear Medicine
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
European Journal of Nuclear Medicine
Subcutaneous sarcoma induced by N ethyl N nitrosourea in rat radiology histo pathology and mutagenesis
Ö., Ö.
, A., Ç., H., E., R, E., F, B. () "
Subcutaneous sarcoma induced by N ethyl N nitrosourea in rat radiology histo pathology and mutagenesis
",
Third European Conference
Ö., Ö.
, A., Ç., H., E., R, E., F, B. () "
Subcutaneous sarcoma induced by N ethyl N nitrosourea in rat radiology histo pathology and mutagenesis
",
Third European Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
Third European Conference
Sister chromatide exchange frequency in women that exposed to biomass in a village of central anatolia
S., S., Z., Ç., İ., A., Ö, Ö., Z, S. () "
Sister chromatide exchange frequency in women that exposed to biomass in a village of central anatolia
",
Third European Conference
S., S., Z., Ç., İ., A., Ö, Ö., Z, S. () "
Sister chromatide exchange frequency in women that exposed to biomass in a village of central anatolia
",
Third European Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
Third European Conference
Increased sister chromatide exchange frequency in tyroid cancer patients that treated with I1313
Çolak, A., Erselcan, T., Süngü, S., Özdemir, S., Orbay, D.,
ÖZDEMİR, Ö.
() "
Increased sister chromatide exchange frequency in tyroid cancer patients that treated with I1313
",
Third European Conference
Çolak, A., Erselcan, T., Süngü, S., Özdemir, S., Orbay, D.,
ÖZDEMİR, Ö.
() "
Increased sister chromatide exchange frequency in tyroid cancer patients that treated with I1313
",
Third European Conference
Kurum Bilgileri
Tıp Fakültesi
Dahili Tıp Bilimleri
Tıbbi Genetik
Özgeçmiş Sayfası
0
Tebliğ/Bildiri
SCI/SSCI/AHCI
ESCI
Scopus
Third European Conference
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