218 results on '"Özbek, Uğur"'
Search Results
2. Digital distraction levels of university students in emergency remote teaching
3. Memantine and SKF82958 but not an enriched environment modulate naloxone-precipitated morphine abstinence syndrome without affecting hippocampal tPA mRNA levels in rats
4. Development of a Mobile-Accessible Web Application in Wound Management: A Pilot Study
5. Should we take precautions to avoid respiratory compromise while delaying CPAP resumption following transsfenoidal surgery? An alternative approach in a patient with severe obstructive sleep apnea: case report
6. Chromosomal breakage and sister chromatid exchange analysis in breast cancer patients with heterozygous BLM gene variants.
7. Traffic analysis of a software defined network
8. Biyobankalar
9. A Novel and Mosaic WDR45 Nonsense Variant Causes Beta-Propeller Protein-Associated Neurodegeneration Identified Through Whole Exome Sequencing and X chromosome Heterozygosity Analysis
10. Chromosomal breakage and sister chromatid exchange analysis in breast cancer patients with heterozygous BLMgene variants
11. Mezankimal Kök Hücre Enkapsülasyonu için 3B Baskı ile Makro Kapsül Üretimi
12. Health Sciences Research: Nursing and Midwifery II
13. High MN1 expression increases the in vitro clonogenic activity of primary mouse B-cells
14. Development of a Mobile-accessible Web Application in Wound Management: A Pilot Study
15. Anti-neuronal and stress-induced-phosphoprotein 1 antibodies in neuro-Behçet's disease
16. Determining T and B Cell development by TREC/KREC analysis in primary immunodeficiency patients and healthy controls
17. Bağlantı ve Tüm Ekzom Dizileme Analizlerinin Birlikte Değerlendirilmesiyle CIC Geninin İzole Distoni Adayı Olarak Belirlenmesi
18. HUKUKUN DİNAMİZMİ: YARGIDA REFORM
19. COMBINED ANALYSIS OF LINKAGE AND WHOLE EXOME SEQUENCING REVEALS CIC AS A CANDIDATE GENE FOR ISOLATED DYSTONIA
20. 1007fs, G908R, R702W Mutations and P268S, IVS8+158 Polymorphisms of the CARD15 Gene in Turkish Inflammatory Bowel Disease Patients and Their Relationship with Disease-Related Surgery
21. Otozomal Resesif Nörogelişimsel Bozukluğun Nedeni Olarak Bi-alelik NALCN Varyantı
22. SET-CAN, the Product of the t(9;9) in Acute Undifferentiated Leukemia, Causes Expansion of Early Hematopoietic Progenitors and Hyperproliferation of Stomach Mucosa in Transgenic Mice
23. Optimizing the Personalized Care for the Management of Rectal Cancer: A Consensus Statement.
24. SCREENING SLC2A1 GENE FOR SEQUENCE AND COPY NUMBER VARIATIONS ASSOCİATED WITH GLUT-1 DEFICIENCY SYNDROME
25. Expression of IFITM1 in chronic myeloid leukemia patients
26. 1007fs, G908R, R702W Mutations and P268S, IVS8+158Polymorphisms of the CARD15 Gene in Turkish Inflammatory Bowel Disease Patients and Their Relationship with Disease-Related Surgery
27. Which may be effective to reduce blood loss after cardiac operations in cyanotic children: tranexamic acid, aprotinin or a combination?
28. Analysis of MYH Tyr165Cys and Gly382Asp variants in childhood leukemias
29. Molecular pathology of haemophilia B in Turkish patients: identification of a large deletion and 33 independent point mutations
30. wt1 Gene Expression in Childhood Acute Leukemias
31. İfade özgürlüğü bağlamında terör örgütünün propagandası suçu
32. ER, SOCS1, p15, E-cadherin and RARB are more Likely to be Members of the Methylator Phenotype of Adult and Childhood AML and Their Methylation is Primarly Regulated by an Overexpression of DNMT 3A
33. PTEN and AKT1 Variations in Childhood T-cell Acute Lymphoblastic Leukemia
34. Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry
35. Aberrant Methylation Profile and Microsatellit Instability in Turkish Sporadic Colorectal Carcinoma
36. The Role of Local Bone Marrow Renin-Angiotensin System in Multiple Myeloma
37. Does normoxemic cardiopulmonary bypass prevent myocardial reoxygenation injury in cyanotic children?
38. Aberrant methylation profile and microsatellit instability in Turkish sporadic colorectal carcinoma
39. Dealing with the gray zones in the management of gastric cancer: the consensus statement of the İstanbul Group
40. PTEN and AKT1 Variations in Childhood T-Cell Acute Lymphoblastic Leukemia.
41. Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia
42. Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span
43. Cerebral Palsy and Genetics
44. EVALUATION OF DISTANCE LEARNING STUDENTS PERFORMANCE USING FUZZY LOGIC
45. 8q24 bölgesi çocukluk çağı lenfoblastik lösemiler için potansiyel risk oluşturur mu?
46. The Role of the Local Bone Marrow Renin-Angiotensin System in Multiple Myeloma.
47. Tüm Genom SNP Genotipleme ile Trizomi 21 ve Ebeveyn Etkisinin Tespiti
48. Dysregulation of the DKK1 gene in pediatric B-cell acute lymphoblastic leukemia
49. Video yardımı ile minimal invazif 'port-akses' kalp cerrahisi erken dönem sonuçları
50. Aberrant Methylation Profile and Microsatellit Instability In Turkish Sporadic Colorectal Carcinoma.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.