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Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

American journal of human genetics, 2007-02, Vol.80 (2), p.338-344

2007

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A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

American journal of human genetics, 2010-05, Vol.86 (5), p.797-804

2010

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Differential expression of selected histone modifier genes in human solid cancers

BMC genomics, 2006-04, Vol.7 (1), p.90-90, Article 90

2006

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p300 CBP and cancer

Oncogene, 2004-05, Vol.23 (24), p.4225-4231

2004

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Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

International journal of pediatric otorhinolaryngology, 2009-05, Vol.73 (5), p.699-705

2009

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Molecular Signatures of Human Chronic Atrial Fibrillation in Primary Mitral Regurgitation

Cardiovascular therapeutics, 2021-10, Vol.2021, p.5516185-12

2021

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Effects of DDT and DDE on placental cholinergic receptors

Reproductive toxicology (Elmsford, N.Y.), 2024-06, Vol.126, p.108588, Article 108588

2024

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Treatment of plasminogen deficiency patients with fresh frozen plasma

Pediatric blood & cancer, 2018-02, Vol.65 (2), p.n/a

2018

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Differentiation and molecular characterization of endothelial progenitor and vascular smooth muscle cells from induced pluripotent stem cells

Bioimpacts, 2023-07, Vol.13 (4), p.289-300

2023

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SLCO1B1 Polymorphisms are Associated With Drug Intolerance in Childhood Leukemia Maintenance Therapy

Journal of pediatric hematology/oncology, 2018-07, Vol.40 (5), p.e289-e294

2018

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Behçet syndrome: The disturbed balance between anti‐ (CLEC12A, CLC) and proinflammatory (IFI27) gene expressions

Immunity, Inflammation and Disease, 2023-04, Vol.11 (4), p.e836-n/a

2023

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Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

PloS one, 2016-02, Vol.11 (2), p.e0149052-e0149052

2016

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From RNA isolation to microarray analysis: Comparison of methods in FFPE tissues

Pathology, research and practice, 2016-08, Vol.212 (8), p.678-685

2016

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Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia

American journal of human genetics, 2010-05, Vol.86 (5), p.789-796

2010

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Isotopic biomarker discovery and application in translational medicine

Drug discovery today, 2010-02, Vol.15 (3), p.127-136

2010

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Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis

PloS one, 2013-05, Vol.8 (5), p.e64016

2013

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Investigation of polymorphic variants of SLC6A4, TPH-1, and TPH-2 genes in cases of completed suicide

Journal of men's health (Amsterdam), 2022-03, Vol.18 (3), p.59

2022

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Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency

Blood coagulation & fibrinolysis, 2016-09, Vol.27 (6), p.637-644

2016

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A 1 Mb minimal amplicon at 8p11-12 in breast cancer identifies new candidate oncogenes

Oncogene, 2005-08, Vol.24 (33), p.5235-5245

2005

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Use of immunohistochemical versus microsatellite analyses as markers for colorectal cancer

Turkish Journal of Biochemistry, 2018-04, Vol.43 (2), p.134-141

2018

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Functionally conserved effects of rapamycin exposure on zebrafish

Molecular medicine reports, 2016-05, Vol.13 (5), p.4421-4430

2016

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Comparison of high-resolution melting analysis to denaturing high performance liquid chromatography in the detection of point mutations in MEFV, F5, and F2 genes

Turkish journal of medical sciences, 2014, Vol.44 (5), p.713-719

2014

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Genetic Profiling of Pediatric Patients with B-Cell Precursor Acute Lymphoblastic Leukemia

Journal of pediatric genetics (Birmingham, Ala.), 2023-12, Vol.12 (4), p.288-300

2023

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C-type lectin domain family 12, member A: A common denominator in Behçet’s syndrome and acute gouty arthritis

Medical hypotheses, 2015-08, Vol.85 (2), p.186-191

2015

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Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

Differential expression of selected histone modifier genes in human solid cancers

p300 CBP and cancer

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

Molecular Signatures of Human Chronic Atrial Fibrillation in Primary Mitral Regurgitation

Effects of DDT and DDE on placental cholinergic receptors

Treatment of plasminogen deficiency patients with fresh frozen plasma

Differentiation and molecular characterization of endothelial progenitor and vascular smooth muscle cells from induced pluripotent stem cells

SLCO1B1 Polymorphisms are Associated With Drug Intolerance in Childhood Leukemia Maintenance Therapy

Behçet syndrome: The disturbed balance between anti‐ (CLEC12A, CLC) and proinflammatory (IFI27) gene expressions

Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

From RNA isolation to microarray analysis: Comparison of methods in FFPE tissues

Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia

Isotopic biomarker discovery and application in translational medicine

Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis

Investigation of polymorphic variants of SLC6A4, TPH-1, and TPH-2 genes in cases of completed suicide

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency

EMSY Links the BRCA2 Pathway to Sporadic Breast and Ovarian Cancer

A 1 Mb minimal amplicon at 8p11-12 in breast cancer identifies new candidate oncogenes

Use of immunohistochemical versus microsatellite analyses as markers for colorectal cancer

Functionally conserved effects of rapamycin exposure on zebrafish

Comparison of high-resolution melting analysis to denaturing high performance liquid chromatography in the detection of point mutations in MEFV, F5, and F2 genes

Genetic Profiling of Pediatric Patients with B-Cell Precursor Acute Lymphoblastic Leukemia

C-type lectin domain family 12, member A: A common denominator in Behçet’s syndrome and acute gouty arthritis

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