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1. SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency.

2. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

3. The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies

4. From Your Nose to Your Toes: A Review of Severe Acute Respiratory Syndrome Coronavirus 2 Pandemic‒Associated Pernio

6. Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction

8. Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

9. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

11. Author Correction: A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection (Nature Immunology, (2022), 23, 2, (159-164), 10.1038/s41590-021-01030-z)

12. Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency

13. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

14. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

16. SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

18. SARS-CoV-2-related MIS-C:A key to the viral and genetic causes of Kawasaki disease?

20. The genetic structure of the Turkish population reveals high levels of variation and admixture

21. Human CRY1 variants associate with attention deficit/hyperactivity disorder

23. Human CRY1 variants associate with attention deficit/hyperactivity disorder

29. Endothelial progenitor cells display clonal restriction in multiple myeloma

30. Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation.

31. A retrospective comparison of allogeneic peripheral blood stem cell and bone marrow transplantation results from a single center: A focus on the incidence of graft-vs.-host disease and relapse

32. A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection

33. Mitochondrial serine protease HTRA2 p.G3999S in a kindred with essential tremor and Parkinson disease

36. Identification of a novel missense mutation in RAD51 in a large family with congenital mirror movements

37. Causal mutation discovery using next generation sequencing data: development and application of a pipeline to reduce false positive calls and to map regions of shared homozygosity and IBD

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48. Circulating endothelial progenitor cells in multiple myeloma: implications and significance

50. cDNA Cloning of the Two Subunits of Human CAAXFarnesyltransferase and Chromosomal Mapping of FNTAand FNTBLoci and Related Sequences

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