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Evaluation of AlphaFold structure-based protein stability prediction on missense variations in cancer

Frontiers in genetics, 2023-02, Vol.14, p.1052383-1052383

2023

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Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas

Journal of neurosurgery, 2018-04, Vol.128 (4), p.1102-1114

2018

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Whole exome sequencing-based analysis to identify DNA damage repair deficiency as a major contributor to gliomagenesis in adult diffuse gliomas

Journal of neurosurgery, 2020-05, Vol.132 (5), p.1435-1446

2020

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Angiogenesis, Invasion, and Metastasis Characteristics of Hepatocellular Carcinoma

Journal of gastrointestinal cancer, 2017-09, Vol.48 (3), p.256-259

2017

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IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation

Scientific reports, 2016-06, Vol.6 (1), p.27569-27569, Article 27569

2016

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Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogenic Mechanisms

Biomedicines, 2020-12, Vol.8 (12), p.574

2020

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Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

BMC medical genomics, 2021-02, Vol.14 (1), p.54-14, Article 54

2021

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Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity

European journal of human genetics : EJHG, 2006-06, Vol.14 (6), p.791-797

2006

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Endothelial progenitor cells display clonal restriction in multiple myeloma

BMC cancer, 2006-06, Vol.6 (1), p.161-161, Article 161

2006

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The SOCS‐1 gene methylation in chronic myeloid leukemia patients

American journal of hematology, 2007-08, Vol.82 (8), p.729-730

2007

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Lack of hotspot mutations other than TP53 R249S in aflatoxin B1 associated hepatocellular carcinoma: Aflatoksin B1 kaynaklı hepatosellüler karsinomlarda özgün TP53 R249S dışındaki mutasyonların eksikliği

Turkish Journal of Biochemistry, 2020-10, Vol.45 (4), p.451-453

2020

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Angiogenesis, Invasion, and Metastasis Characteristics of Hepatocellular Carcinoma

Journal of gastrointestinal cancer, 2017, Vol.48 (3), p.256-259

2017

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Toward In Vitro Epigenetic Drug Design for Thyroid Cancer: The Promise of PF-03814735, an Aurora Kinase Inhibitor

Omics (Larchmont, N.Y.), 2019-10, Vol.23 (10), p.486

2019

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Lack of hotspot mutations other than TP53 R249S in aflatoxin B1 associated hepatocellular carcinoma

Turkish Journal of Biochemistry, 2020-04, Vol.45 (4), p.451-453

2020

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Lack of Association Between RNASEL Arg462Gln Variant and the Risk of Breast Cancer

Anticancer research, 2004-07, Vol.24 (4), p.2547-2549

2004

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Yeni Nesil Dizileme Teknolojileri İle Kanserde Mitokondriyal DNA Analizi

Harran Üniversitesi Tıp Fakültesi Dergisi, 2021-04, Vol.18 (1), p.40-44

2021

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JAK2V617F Mutation in Patients with Portal Vein Thrombosis

Digestive diseases and sciences, 2008-10, Vol.53 (10), p.2778-2783

2008

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Analysis of MYH Tyr165Cys and Gly382Asp variants in childhood leukemias

Journal of cancer research and clinical oncology, 2003-10, Vol.129 (10), p.604-605

2003

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Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy

European journal of human genetics : EJHG, 2002-01, Vol.10 (1), p.77-81

2002

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Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion

Australian & New Zealand journal of obstetrics & gynaecology, 2006-10, Vol.46 (5), p.384-387

2006

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Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and bladder cancer susceptibility in the Turkish population

Archives of toxicology, 2001-10, Vol.75 (8), p.459-464

2001

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Evidence for Clonality in Circulating Endothelial Progenitor Cells in Multiple Myeloma

Blood, 2004-11, Vol.104 (11), p.2357-2357

2004

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Analysis of Candidate Molecular Targets in Adult (CML) and Childhood (AML, ALL) Leukemias

Boylu, Cemaliye Akyerli

2004

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Analysis of hMLH1 Germline Mutations in Three Turkish Hereditary Nonpolyposis Colorectal Cancer Kindreds

Akyerli, Cemaliye

1998

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Skewed X chromosome inactivation in blood cells of women with scleroderma

Arthritis and rheumatism, 2005-05, Vol.52 (5), p.1564-1570

2005

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Evaluation of AlphaFold structure-based protein stability prediction on missense variations in cancer

Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas

Whole exome sequencing-based analysis to identify DNA damage repair deficiency as a major contributor to gliomagenesis in adult diffuse gliomas

Angiogenesis, Invasion, and Metastasis Characteristics of Hepatocellular Carcinoma

IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation

Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogenic Mechanisms

Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity

Endothelial progenitor cells display clonal restriction in multiple myeloma

The SOCS‐1 gene methylation in chronic myeloid leukemia patients

Lack of hotspot mutations other than TP53 R249S in aflatoxin B1 associated hepatocellular carcinoma: Aflatoksin B1 kaynaklı hepatosellüler karsinomlarda özgün TP53 R249S dışındaki mutasyonların eksikliği

Angiogenesis, Invasion, and Metastasis Characteristics of Hepatocellular Carcinoma

Toward In Vitro Epigenetic Drug Design for Thyroid Cancer: The Promise of PF-03814735, an Aurora Kinase Inhibitor

Lack of hotspot mutations other than TP53 R249S in aflatoxin B1 associated hepatocellular carcinoma

Lack of Association Between RNASEL Arg462Gln Variant and the Risk of Breast Cancer

Yeni Nesil Dizileme Teknolojileri İle Kanserde Mitokondriyal DNA Analizi

JAK2V617F Mutation in Patients with Portal Vein Thrombosis

Analysis of MYH Tyr165Cys and Gly382Asp variants in childhood leukemias

Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy

Extremely skewed X-chromosome inactivation patterns in women with recurrent spontaneous abortion

Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and bladder cancer susceptibility in the Turkish population

Evidence for Clonality in Circulating Endothelial Progenitor Cells in Multiple Myeloma

Analysis of Candidate Molecular Targets in Adult (CML) and Childhood (AML, ALL) Leukemias

Analysis of hMLH1 Germline Mutations in Three Turkish Hereditary Nonpolyposis Colorectal Cancer Kindreds

Skewed X chromosome inactivation in blood cells of women with scleroderma

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