Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Diğer Dergilerde Yayınlanan Makaleler

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Crosstalk Between T-Cadherin and Wnt/B-Catenin Pathways in Cancer

European Society of Human Genetics Conference (ESHG) 2009, Vienna, Avusturya, 23 - 26 Mayıs 2009, ss.166 Creative Commons License Sürdürülebilir Kalkınma

Decreased WNT5A and FZ5 mRNA Levels contributes to Acute Lymphoblastic Leukemia (ALL)

30th World Congress of the International Society of Hematology, İstanbul, Türkiye, ss.196

IKZF1 Deletions at Diagnose and Relapse of Childhood B-ALL

59th Annual Meeting of the American-Society-of-Hematology (ASH), Georgia, Amerika Birleşik Devletleri, 9 - 12 Aralık 2017, cilt.130 identifier

Turkish National Severe Congenital Neutropenia Registry

58th Annual Meeting and Exposition of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 3 - 06 Aralık 2016, cilt.128 identifier

Real-Life Data and a Single Center Experience on the Efficacy and Toxicity Profile of Imatinib in the Treatment of Elderly Patients with Chronic Myeloid Leukemia

58th Annual Meeting and Exposition of the American-Society-of-Hematology (ASH), California, Amerika Birleşik Devletleri, 3 - 06 Aralık 2016, cilt.128 identifier

T- ALL hücre hatlarında SKIL geni ve hsa-miR223 fonksiyonel ilişkisi

14. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Türkiye, 27 - 30 Ekim 2015, ss.52

Detection of CD19, ICOS, TACI gene mutations in Turkish CVID patients

4th European Congress of Immunology Vienna 2015, Vienna, Avusturya, 6 - 09 Eylül 2015, ss.96

Primer antikor yetersizlik hastalarında moleküler tanı.

DETAE Genç Araştırıcılar Toplantısı 2015, İstanbul, Türkiye, 19 - 20 Ocak 2015, ss.15-16

DETAE Genç Araştırıcılar Toplantısı 2015

Primer immün yetersizliklerde genetik alt yapının yeni dizileme yöntemi ile belirlenmesi., İstanbul, Türkiye, 19 - 20 Ocak 2015, ss.16-17

Primer antikor yetersizlik hastalarında Moleküler tanı.

6. DETAE günleri; DETAE’nin 70. Yaşında hastalık ve sağlığa bakış, İstanbul, Türkiye, 24 - 25 Kasım 2014, ss.28

Epigenetic profile of early relapsed Childhood ALL

40 Ulusal Hematoloji Kongresi, Antalya, Türkiye, 22 - 25 Ekim 2014, ss.20

Molecular analysis of consanguineous rare syndromes in Turkey

European Biotechnology Congress, Lecce, İtalya, 15 - 18 Mayıs 2014, cilt.185 identifier

Two novel mutations of BTK gene in Turkish patients diagnosed with X-Linked Agammaglobulinemia.

2nd International Molecular Immunology and Immunogenetics Congress (MIMIC-II), Antalya, Türkiye, 27 - 30 Nisan 2014, ss.66

The role of cytokine gene polymorphism and oxidant/antioxidant status in recurrent aphthous stomatitis

6th European Meeting of Association of Basic Science Teachers in Dentistry, Madrid, İspanya, 6 - 08 Nisan 2014, ss.44

X’e Bağlı Agammaglobulinemi (Xla) Hastalarında Btk Gen Mutasyonlarının Araştırılması Ve İki Yeni Mutasyon.

5. DETAE Günleri; Deneysel araştırmalar ve kliniğe yansımalar,, İstanbul, Türkiye, 11 - 12 Kasım 2013, ss.39

BTK protein determination by flow cytometry in patients with X-LA.

Molecular Immunology & Immunogenetics Congress, Antalya, Türkiye, 27 - 30 Nisan 2012, cilt.1, ss.116-117 Creative Commons License

Multidrug Resistance Gene (MDR1) C3435T Polymorphism and Imatinib Response in Patients with Chronic Myeloid Leukemia

53rd Annual Meeting and Exposition of the American-Society-of-Hematology (ASH)/Symposium on the Basic Science of Hemostasis and Thrombosis, California, Amerika Birleşik Devletleri, 10 - 13 Aralık 2011, cilt.118, ss.736 identifier

Estimating the prevalence of autosomal recessive disorders through mutational records: the homozygosity index

European Biotechnology Congress, İstanbul, Türkiye, 28 Eylül - 01 Ekim 2011, cilt.22 identifier

Harmonized Testing for BCR-ABL Kinase Domain Mutations In CML: Results of a Survey and First Control Round within 28 National Reference Laboratories In Europe

52nd Annual Meeting of the American-Society-of-Hematology (ASH), Florida, Amerika Birleşik Devletleri, 4 - 07 Aralık 2010, cilt.116, ss.392-393 identifier

Stability of Conversion Factors for BCR-ABL Monitoring - Implications for the Frequency of Validation Rounds

52nd Annual Meeting of the American-Society-of-Hematology (ASH), Florida, Amerika Birleşik Devletleri, 4 - 07 Aralık 2010, cilt.116, ss.392 identifier

Mutations in AXIN1, APC and B-catenin Genes in T-cell Acute Leukemia Patients

T-cell Acute Lymphoblastic Leukemia (T-ALL) Meets Normal T-cell Development, Mandelieu, Fransa, 7 - 09 Mayıs 2010, ss.28

WNT pathway mutations in acute leukemia patients

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.55 identifier

WNT5A gene expression and promoter methylation in acute leukemia patients

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.55 identifier

Methylation status of the wnt antagonist DICKKOPF-1 gene in acute leukemias

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.403 identifier

Increased level of B-catenin mRNA and mutational alterations in APC gene are present in acute leukemia

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.62 identifier

Different activation of WNT signaling pathway in B-cell and T-cell acute leukemias.

48th Annual Meeting of the American-Society-of-Hematology, Florida, Amerika Birleşik Devletleri, 9 - 12 Aralık 2006, cilt.108 identifier

11 beta-HSD type 1 is responsible for low plasma hdl-cholesterol and abdominal obesity in metabolic syndrome patients

31st Congress of the Federation-of-European-Biochemical-Societies (FEBS), İstanbul, Türkiye, 24 - 29 Haziran 2006, cilt.273, ss.203 Sürdürülebilir Kalkınma identifier

The role of FABP4 gene expression in metabolic syndrome patients with previous myocardial infarction

31st Congress of the Federation-of-European-Biochemical-Societies (FEBS), İstanbul, Türkiye, 24 - 29 Haziran 2006, cilt.273, ss.204 identifier

Quantitative expression analysis of glucocorticoid receptor (GcR) gene in metabolic syndrome

31st Congress of the Federation-of-European-Biochemical-Societies (FEBS), İstanbul, Türkiye, 24 - 29 Haziran 2006, cilt.273, ss.204 identifier

Acylation stimulating protein and complement c3 mRNA expression in metabolic syndrome

31st Congress of the Federation-of-European-Biochemical-Societies (FEBS), İstanbul, Türkiye, 24 - 29 Haziran 2006, cilt.273, ss.205 identifier

Relationship between DNA index and cellular drug resistance in children with newly diagnosed acute lymphoblastic leukemia.

46th Annual Meeting of the American-Society-of-Hematology, California, Amerika Birleşik Devletleri, 4 - 07 Aralık 2004, cilt.104 identifier

Effect of methylenetetrahydrofolate reductase gene polymorphism on methotrexate toxicity after bone marrow transplantation

29th Annual Meeting of the European Group for Blood and Marrow Transplantation/19th Meeting of the EBMT Nurses Group/2nd Meeting of the EBMT Data Management Group, İstanbul, Türkiye, 23 - 26 Mart 2003, cilt.31 identifier

Allelotype frequencies of TPMT (thiopurine S-methyltransferase), CYP3A4 and CYP3A5 genes in Turkish population

5th International Symposium on Leukemia and Lymphoma, Amsterdam, Hollanda, 12 - 15 Mart 2003, cilt.17, ss.679 identifier

Kitap & Kitap Bölümleri

Hematolojik Malign Hastalıklar, Lökomogenez, Moleküler Özellikleri

Pediatrik Hematoloji, Prof. Dr. S.Sema Anak, Editör, İstanbul Medikal Yayıncılık, İstanbul, ss.565-577, 2011

Metrikler

Yayın

141

Atıf (WoS)

941

H-İndeks (WoS)

17

Atıf (Scopus)

1042

H-İndeks (Scopus)

16

Proje

45

Tez Danışmanlığı

1

Açık Erişim

2
BM Sürdürülebilir Kalkınma Amaçları