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Differential expression of inflammasome regulatory transcripts in periodontal disease

Journal of periodontology (1970), 2020-05, Vol.91 (5), p.606-616

2020

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Next-Generation Sequencing Analysis of MVK, NLRP3, TNFRSF1A, and PSTPIP1 Genes in Patients without MEFV Gene Variation and Genotype-Phenotype Correlation

European journal of rheumatology, 2022-04, Vol.9 (2), p.62-67

2022

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A rare cause of urolithiasis in an infant: Questions

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.2065-2065

2021

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A rare cause of urolithiasis in an infant: Answers

Pediatric nephrology (Berlin, West), 2021-07, Vol.36 (7), p.2067-2068

2021

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NPHS2 gene mutations in azerbaijani children with steroid-resistant nephrotic syndrome

Saudi journal of kidney diseases and transplantation, 2020-01, Vol.31 (1), p.144-149

2020

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TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome

Journal of the American Society of Nephrology, 2019-12, Vol.30 (12), p.2338-2353

2019

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Treatment of familial mediterranean fever with canakinumab in patients who are unresponsive to colchicine

European journal of rheumatology, 2019-04, Vol.6 (2), p.85-85

2019

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Effects of bodybuilding and protein supplements in saliva, gingival crevicular fluid, and serum

Journal of Oral Science, 2017, Vol.59(1), pp.121-130

2017

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A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment

Turkish journal of pediatrics, 2018-10, Vol.60 (5), p.588-592

2018

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Evaluation of Renin, Aldosterone, Angiotensin, and Lipid Metabolism Genes and Genotype-Phenotype Relationship in Childhood Primary Hypertension Pathogenesis

Turkish journal of nephrology, 2022-10, Vol.31 (4), p.368-374

2022

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Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference

Clinical case reports, 2021-04, Vol.9 (4), p.2023-2031

2021

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Matrix Metalloproteinase (MMP)‐8 and Tissue Inhibitor of MMP‐1 (TIMP‐1) Gene Polymorphisms in Generalized Aggressive Periodontitis: Gingival Crevicular Fluid MMP‐8 and TIMP‐1 Levels and Outcome of Periodontal Therapy

Journal of periodontology (1970), 2014-08, Vol.85 (8), p.1070-1080

2014

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Genotypic and Phenotypic Features of Both NPHS1 and NPHS2 Genes in Infantile Nephrotic Syndrome and Prognostic Effect of E117K Polymorphism in NPHS1 Gene

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2019-04, Vol.In Press (In Press)

2019

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FAS/FASL gene polymorphisms in Turkish patients with chronic myeloproliferative disorders

Archives of medical science, 2017-03, Vol.13 (2), p.426-432

2017

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NOD2/CARD15 gene mutations in patients with gouty arthritis

Bosnian journal of basic medical sciences, 2016-11, Vol.16 (4), p.276-279

2016

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A Rare Case of Cholestasis: Arthrogryposis, Renal Tubular Disorder and Cholestasis Syndrome

The journal of pediatric research, 2018-09, Vol.5 (3), p.161-163

2018

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Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation

Pediatrics international, 2015-02, Vol.57 (1), p.177-179

2015

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Myostatin Gene Polymorphism in an Elderly Sarcopenic Turkish Population

Genetic testing and molecular biomarkers, 2015-08, Vol.19 (8), p.457

2015

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Novel VPS33B mutations of G514S gene cause an arthrogryposis, renal dysfunction and cholestasis syndrome

International Journal of Case Reports and Images (IJCRI), 2016-04, Vol.7 (4), p.216

2016

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MEFV gene allele frequency and genotype distribution in 3230 patients’ analyses by next generation sequencing methods

Gene, 2022-06, Vol.827, p.146447-146447, Article 146447

2022

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Individual and Combined Effects of Selective Cyclooxygenase‐2 Inhibitor and Omega‐3 Fatty Acid on Endotoxin‐Induced Periodontitis in Rats

Journal of periodontology (1970), 2005-01, Vol.76 (1), p.99-106

2005

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Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency

Italian journal of pediatrics, 2012-03, Vol.38 (1), p.8-8, Article 8

2012

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Escherichia coli brain abscess in a twin pair associated with TLR4 gene mutation

Pediatrics international, 2013-08, Vol.55 (4), p.516-518

2013

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Gene polymorphisms of matrix metalloproteinase-2, -9 and -12 in periodontal health and severe chronic periodontitis

Archives of oral biology, 2008-04, Vol.53 (4), p.337-345

2008

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Differential expression of inflammasome regulatory transcripts in periodontal disease

Next-Generation Sequencing Analysis of MVK, NLRP3, TNFRSF1A, and PSTPIP1 Genes in Patients without MEFV Gene Variation and Genotype-Phenotype Correlation

A rare cause of urolithiasis in an infant: Questions

A rare cause of urolithiasis in an infant: Answers

NPHS2 gene mutations in azerbaijani children with steroid-resistant nephrotic syndrome

TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome

Treatment of familial mediterranean fever with canakinumab in patients who are unresponsive to colchicine

Effects of bodybuilding and protein supplements in saliva, gingival crevicular fluid, and serum

Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome

A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment

Evaluation of Renin, Aldosterone, Angiotensin, and Lipid Metabolism Genes and Genotype-Phenotype Relationship in Childhood Primary Hypertension Pathogenesis

Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference

Matrix Metalloproteinase (MMP)‐8 and Tissue Inhibitor of MMP‐1 (TIMP‐1) Gene Polymorphisms in Generalized Aggressive Periodontitis: Gingival Crevicular Fluid MMP‐8 and TIMP‐1 Levels and Outcome of Periodontal Therapy

Genotypic and Phenotypic Features of Both NPHS1 and NPHS2 Genes in Infantile Nephrotic Syndrome and Prognostic Effect of E117K Polymorphism in NPHS1 Gene

FAS/FASL gene polymorphisms in Turkish patients with chronic myeloproliferative disorders

NOD2/CARD15 gene mutations in patients with gouty arthritis

A Rare Case of Cholestasis: Arthrogryposis, Renal Tubular Disorder and Cholestasis Syndrome

Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation

Myostatin Gene Polymorphism in an Elderly Sarcopenic Turkish Population

Novel VPS33B mutations of G514S gene cause an arthrogryposis, renal dysfunction and cholestasis syndrome

MEFV gene allele frequency and genotype distribution in 3230 patients’ analyses by next generation sequencing methods

Individual and Combined Effects of Selective Cyclooxygenase‐2 Inhibitor and Omega‐3 Fatty Acid on Endotoxin‐Induced Periodontitis in Rats

Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency

Escherichia coli brain abscess in a twin pair associated with TLR4 gene mutation

Gene polymorphisms of matrix metalloproteinase-2, -9 and -12 in periodontal health and severe chronic periodontitis

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