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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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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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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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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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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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p300 CBP and cancer

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

2004

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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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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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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 Regulates p53-Dependent Apoptosis after DNA Damage in Colorectal Cancer Cells by Modulation of PUMA/p21 Levels

Proceedings of the National Academy of Sciences - PNAS, 2004-05, Vol.101 (19), p.7386-7391

2004

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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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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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Effects of DDT and DDE on placental cholinergic receptors

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

2024

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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'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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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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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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Transcriptomic evaluation of metals detected in placenta

Chemosphere (Oxford), 2024-09, Vol.363, p.142929, Article 142929

2024

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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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Biologic tumor behavior in pilocytic astrocytomas

Child's nervous system, 2012-03, Vol.28 (3), p.375-389

2012

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

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

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

Treatment of plasminogen deficiency patients with fresh frozen plasma

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

p300 CBP and cancer

Functionally conserved effects of rapamycin exposure on zebrafish

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

Differential expression of selected histone modifier genes in human solid cancers

p300 Regulates p53-Dependent Apoptosis after DNA Damage in Colorectal Cancer Cells by Modulation of PUMA/p21 Levels

Protocol for qRT-PCR analysis from formalin fixed paraffin embedded tissue sections from diffuse large b-cell lymphoma: Validation of the six-gene predictor score

Molecular Signatures of Human Chronic Atrial Fibrillation in Primary Mitral Regurgitation

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

Effects of DDT and DDE on placental cholinergic receptors

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

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

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

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

Transcriptomic evaluation of metals detected in placenta

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

Biologic tumor behavior in pilocytic astrocytomas

Isotopic biomarker discovery and application in translational medicine

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