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Promoter methylation and expression changes of CDH1 and P16 genes in invasive breast cancer and adjacent normal breast tissue

Neoplasma, 2010, Vol.57 (5), p.465

2010

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beta-catenin gene mutation in invasive ductal breast cancer

Journal of B.U. ON., 2008-10, Vol.13 (4), p.533

2008

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1045 Human epidermal growth factor receptor 2 (HER2) testing in operable breast cancer: comparison of immunohistochemistry (IHC), fluorescent in situ hybridization (FISH), chromogenic in situ hybridization (CISH), and quantitative real-time polymerase chain reaction (qRT-PCR)

European journal of cancer supplements, 2009, Vol.7 (2), p.99-100

2009

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5093 Beta-catenin stability, frizzled and cyclin D1 proteins expression in human breast cancer and its relation with their prognosis

European journal of cancer supplements, 2009, Vol.7 (2), p.288-288

2009

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Selecting housekeeping genes as references for the normalization of quantitative PCR data in breast cancer

Clinical & translational oncology, 2014-02, Vol.16 (2), p.184-190

2014

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Genome-Wide Gene Expression Analysis of NIH 3T3 Cell Line Under Mechanical Stimulation

Cellular and molecular bioengineering, 2011-03, Vol.4 (1), p.46-55

2011

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Consistent Loss of Heterozygosity at 14q32 in Lymphoid Blast Crisis of Chronic Myeloid Leukemia

Leukemia & lymphoma, 2000, Vol.39 (3-4), p.385-390

2000

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Correlation of clinical data and expression levels of six tumor supressor genes in breast cancer

Cancer research (Chicago, Ill.), 2009-01, Vol.69 (2_Supplement), p.1058

2009

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Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11β-hydroxylase deficiency

Journal of endocrinological investigation, 2007-04, Vol.30 (4), p.285-291

2007

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Hyperbilirubinemic serum is cytotoxic and induces apoptosis in murine astrocytes

Biology of the neonate, 2005-01, Vol.87 (2), p.99-104

2005

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Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11beta-hydroxylase deficiency

Journal of endocrinological investigation, 2007-04, Vol.30 (4), p.285-291

2007

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Analysis of cytotoxic T lymphocyte antigen-4 (CTLA-4) exon 1 polymorphism in patients with type 1 diabetes mellitus in a Turkish population

Journal of pediatric endocrinology & metabolism : JPEM, 2004-05, Vol.17 (5), p.731

2004

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A case of mixed gonadal dysgenesis with 45 X/46 XY karyotype and aortic coarctation

The Journal of pediatric endocrinology, 1993-04, Vol.6 (2), p.191

1993

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BRCA1, C-erbB-2, and H-ras gene expressions in young women with breast cancer. An immunohistochemical study

Applied immunohistochemistry & molecular morphology, 2000-03, Vol.8 (1), p.12

2000

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Mosaic form (45X/46XX) of Turner's syndrome. A case report

Journal of reproductive medicine, 2002-12, Vol.47 (12), p.1053

2002

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Microsatellite Instability in Early-onset Breast Cancer

Pathology, research and practice, 2002, Vol.198 (8), p.525-530

2002

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Effect of cytomegalovirus on adult human chromosomes

Acta virologica (Anglickâa verze), 1981-07, Vol.25 (4), p.248

1981

Volltextzugriff (PDF)

Microsatellite instability is a rare phenomenon in transition from chronic to blastic phase chronic myeloid leukemia

Turkish journal of cancer, 2001, Vol.31 (2), p.63-71

2001

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Preclinical medical training using the integrated system in dokuz eylül university medical school

Biochemical education, 1995, Vol.23 (1), p.21-24

1995

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Developing an in-vitro mechanical stretching system for moleculer cell biology studies (in English)

2009 14th National Biomedical Engineering Meeting, 2009, p.1-5

2009

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Pelger‐Huet anomaly with trisomy‐18 syndrome

American journal of hematology, 1993-08, Vol.43 (4), p.328-329

1993

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DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors

Cancer genetics and cytogenetics, 2003-09, Vol.145 (2), p.108-114

2003

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Two brothers with a 7.0 kb gene deletion associated with isolated growth hormone deficiency type 1A

Journal of pediatric endocrinology & metabolism : JPEM, 1996-05, Vol.9 (3), p.423

1996

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A Turkish family with 6.7 Kb deletion associated with isolated growth hormone deficiency type 1A

Turkish journal of pediatrics, 1997-01, Vol.39 (1), p.99

1997

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Trisomy 18 evaluated by Marion's scoring system

Indian journal of pediatrics, 1992-07, Vol.59 (4), p.537-540

1992

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Promoter methylation and expression changes of CDH1 and P16 genes in invasive breast cancer and adjacent normal breast tissue

beta-catenin gene mutation in invasive ductal breast cancer

1045 Human epidermal growth factor receptor 2 (HER2) testing in operable breast cancer: comparison of immunohistochemistry (IHC), fluorescent in situ hybridization (FISH), chromogenic in situ hybridization (CISH), and quantitative real-time polymerase chain reaction (qRT-PCR)

5093 Beta-catenin stability, frizzled and cyclin D1 proteins expression in human breast cancer and its relation with their prognosis

Selecting housekeeping genes as references for the normalization of quantitative PCR data in breast cancer

Genome-Wide Gene Expression Analysis of NIH 3T3 Cell Line Under Mechanical Stimulation

Consistent Loss of Heterozygosity at 14q32 in Lymphoid Blast Crisis of Chronic Myeloid Leukemia

Correlation of clinical data and expression levels of six tumor supressor genes in breast cancer

Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11β-hydroxylase deficiency

Hyperbilirubinemic serum is cytotoxic and induces apoptosis in murine astrocytes

Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11beta-hydroxylase deficiency

Analysis of cytotoxic T lymphocyte antigen-4 (CTLA-4) exon 1 polymorphism in patients with type 1 diabetes mellitus in a Turkish population

A case of mixed gonadal dysgenesis with 45 X/46 XY karyotype and aortic coarctation

BRCA1, C-erbB-2, and H-ras gene expressions in young women with breast cancer. An immunohistochemical study

Mosaic form (45X/46XX) of Turner's syndrome. A case report

Microsatellite Instability in Early-onset Breast Cancer

Effect of cytomegalovirus on adult human chromosomes

Microsatellite instability is a rare phenomenon in transition from chronic to blastic phase chronic myeloid leukemia

Preclinical medical training using the integrated system in dokuz eylül university medical school

Developing an in-vitro mechanical stretching system for moleculer cell biology studies (in English)

Pelger‐Huet anomaly with trisomy‐18 syndrome

DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors

Two brothers with a 7.0 kb gene deletion associated with isolated growth hormone deficiency type 1A

A Turkish family with 6.7 Kb deletion associated with isolated growth hormone deficiency type 1A

Trisomy 18 evaluated by Marion's scoring system

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