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Severe influenza virus infection in children admitted to the PICU: Comparison of influenza A and influenza B virus infection

Journal of medical virology, 2022-02, Vol.94 (2), p.575-581

2022

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Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation

Scientific reports, 2022-10, Vol.12 (1), p.16984-16984, Article 16984

2022

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Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects

Brain, behavior, and immunity, 2022-08, Vol.104, p.183-190

2022

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Var3PPred: variant prediction based on 3-D structure and sequence analyses of protein-protein interactions on autoinflammatory diseases

PeerJ (San Francisco, CA), 2024-05, Vol.12, p.e17297, Article e17297

2024

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Clinical, imaging and genotypical features of three deceased and five surviving cases with ADA2 deficiency

Rheumatology international, 2018, Vol.38 (1), p.129-136

2018

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Peripheral blood mononuclear cell proteome profile in Behçet’s syndrome

Rheumatology international, 2020, Vol.40 (1), p.65-74

2020

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LACC1 deficiency links juvenile arthritis with autophagy and metabolism in macrophages

The Journal of experimental medicine, 2021-03, Vol.218 (3)

2021

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A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-α

Paediatrics and international child health, 2020-01, Vol.40 (1), p.65-68

2020

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A two-step purification platform for efficient removal of Fab-related impurities: A case study for Ranibizumab

Heliyon, 2023-11, Vol.9 (11), p.e21001-e21001, Article e21001

2023

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Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic data

PeerJ (San Francisco, CA), 2021-09, Vol.9, p.e11922, Article e11922

2021

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Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever

BMC medical genetics, 2011-08, Vol.12 (1), p.105-105, Article 105

2011

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Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic cerebrospinal fluid markers

PloS one, 2023-06, Vol.18 (6), p.e0287463-e0287463

2023

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CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes

PloS one, 2015-05, Vol.10 (5), p.e0122045-e0122045

2015

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A novel BH3 mimetic Bcl-2 inhibitor promotes autophagic cell death and reduces in vivo Glioblastoma tumor growth

Cell death discovery, 2022-10, Vol.8 (1), p.433-433, Article 433

2022

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Translation of Cellular Senescence to Novel Therapeutics: Insights From Alternative Tools and Models

Frontiers in aging, 2022-06, Vol.3, p.828058

2022

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Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in Turkey

Frontiers in pediatrics, 2022-06, Vol.10, p.926013-926013

2022

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A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

Turkish journal of haematology, 2019-02, Vol.36 (1), p.29-36

2019

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Transcriptomics and Proteomics Analyses Reveal JAK Signaling and Inflammatory Phenotypes during Cellular Senescence in Blind Mole Rats: The Reflections of Superior Biology

Biology (Basel, Switzerland), 2022-08, Vol.11 (9), p.1253

2022

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COVID-19 vaccine candidates and vaccine development platforms available worldwide

Journal of pharmaceutical analysis, 2021-12, Vol.11 (6), p.675-682

2021

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Severe lupin bean intoxication: an anticholinergic toxidrome

대한소아응급의학회지, 2021, 8(2), , pp.108-111

2021

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Quality assurance of genetic laboratories and the EBTNA practice certification, a simple standardization assurance system for a laboratory network

The eurobiotech journal, 2018-10, Vol.2 (4), p.215-222

2018

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Evaluation of the results of the patients who underwent plasmapheresis in the pediatric intensive care unit

Turkish journal of medical sciences, 2024-01, Vol.54 (3), p.508-516

2024

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Alternatively spliced MEFV transcript lacking exon 2 and its protein isoform pyrin-2d implies an epigenetic regulation of the gene in inflammatory cell culture models

Genetics and molecular biology, 2017-07, Vol.40 (3), p.688-697

2017

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Our Treatment Experience in Poisoning With Calcium Channel Blockers: A Series of Twelve Cases

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2024-02, Vol.34 (1)

2024

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Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype

Rheumatology (Oxford, England), 2023-09, Vol.62 (9), p.3188-3196

2023

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Severe influenza virus infection in children admitted to the PICU: Comparison of influenza A and influenza B virus infection

Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation

Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects

Var3PPred: variant prediction based on 3-D structure and sequence analyses of protein-protein interactions on autoinflammatory diseases

Clinical, imaging and genotypical features of three deceased and five surviving cases with ADA2 deficiency

Peripheral blood mononuclear cell proteome profile in Behçet’s syndrome

LACC1 deficiency links juvenile arthritis with autophagy and metabolism in macrophages

A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-α

A two-step purification platform for efficient removal of Fab-related impurities: A case study for Ranibizumab

Investigation of multiple sclerosis-related pathways through the integration of genomic and proteomic data

Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever

Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic cerebrospinal fluid markers

CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes

A novel BH3 mimetic Bcl-2 inhibitor promotes autophagic cell death and reduces in vivo Glioblastoma tumor growth

Translation of Cellular Senescence to Novel Therapeutics: Insights From Alternative Tools and Models

Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in Turkey

A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

Transcriptomics and Proteomics Analyses Reveal JAK Signaling and Inflammatory Phenotypes during Cellular Senescence in Blind Mole Rats: The Reflections of Superior Biology

COVID-19 vaccine candidates and vaccine development platforms available worldwide

Severe lupin bean intoxication: an anticholinergic toxidrome

Quality assurance of genetic laboratories and the EBTNA practice certification, a simple standardization assurance system for a laboratory network

Evaluation of the results of the patients who underwent plasmapheresis in the pediatric intensive care unit

Alternatively spliced MEFV transcript lacking exon 2 and its protein isoform pyrin-2d implies an epigenetic regulation of the gene in inflammatory cell culture models

Our Treatment Experience in Poisoning With Calcium Channel Blockers: A Series of Twelve Cases

Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype

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