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Comprehensive Mapping of Histone Modifications at DNA Double-Strand Breaks Deciphers Repair Pathway Chromatin Signatures

Molecular cell, 2018-10, Vol.72 (2), p.250-262.e6

2018

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Genome-wide mapping of long-range contacts unveils clustering of DNA double-strand breaks at damaged active genes

Nature structural & molecular biology, 2017-04, Vol.24 (4), p.353

2017

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Topoisomerase 1 prevents replication stress at R-loop-enriched transcription termination sites

Nature communications, 2020-08, Vol.11 (1), p.3940-12, Article 3940

2020

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qDSB-Seq is a general method for genome-wide quantification of DNA double-strand breaks using sequencing

Nature communications, 2019-05, Vol.10 (1), p.2313-2313, Article 2313

2019

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Smad3 Signaling Promotes Fibrosis While Preserving Cardiac and Aortic Geometry in Obese Diabetic Mice

Circulation. Heart failure, 2015-07, Vol.8 (4), p.788-798

2015

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Endogenous Thrombospondin 1 Protects the Pressure-Overloaded Myocardium by Modulating Fibroblast Phenotype and Matrix Metabolism

Hypertension (Dallas, Tex. 1979), 2011-11, Vol.58 (5), p.902-911

2011

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Feasibility Study of a Novel Protease-Activated Fluorescent Imaging System for Real-Time, Intraoperative Detection of Residual Breast Cancer in Breast Conserving Surgery

Annals of surgical oncology, 2020-06, Vol.27 (6), p.1854-1861

2020

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Wybrane współczesne biblioteki parafialne na terenie dzielnicy Wrocławia - Fabryczna : stan badań na rok 1996/1997

Archiwa biblioteki i muzea kościelne, 2020-04, Vol.74, p.7-46

2020

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Exposure of Keratinocytes to Candida Albicans in the Context of Atopic Milieu Induces Changes in the Surface Glycosylation Pattern of Small Extracellular Vesicles to Enhance Their Propensity to Interact With Inhibitory Siglec Receptors

Frontiers in immunology, 2022-06, Vol.13, p.884530-884530

2022

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Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy

Scientific reports, 2017-06, Vol.7 (1), p.3362-5, Article 3362

2017

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The potential utility of re-mining results of somatic mutation testing: KRAS status in lung adenocarcinoma

Cancer genetics, 2016-05, Vol.209 (5), p.195-198

2016

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Lung adenocarcinomas with isolated TP53 mutation: A comprehensive clinical, cytopathologic and molecular characterization

Cancer medicine (Malden, MA), 2024-01, Vol.13 (1), p.e6873-n/a

2024

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Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit

Journal of clinical medicine, 2020-07, Vol.9 (7), p.2220

2020

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Novel de novo mutation affecting two adjacent aminoacids in the EED gene in a patient with Weaver syndrome

Journal of human genetics, 2018-04, Vol.63 (4), p.517-520

2018

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Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines

Clinical genetics, 2018-12, Vol.94 (6), p.581-585

2018

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Combined MEK and VEGFR Inhibition in Orthotopic Human Lung Cancer Models Results in Enhanced Inhibition of Tumor Angiogenesis, Growth, and Metastasis

Clinical cancer research, 2012-03, Vol.18 (6), p.1641-1654

2012

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Brain Tissue Low-Level Mosaicism for MTOR Mutation Causes Smith–Kingsmore Phenotype with Recurrent Hypoglycemia—A Novel Phenotype and a Further Proof for Testing of an Affected Tissue

Diagnostics (Basel), 2021-07, Vol.11 (7), p.1269

2021

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Applications of nanodosimetry in particle therapy planning and beyond

Physics in medicine & biology, 2021-12, Vol.66 (24), p.24

2021

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TGF-β signaling in fibrosis

Growth factors (Chur, Switzerland), 2011-10, Vol.29 (5), p.196-202

2011

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Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes

Journal of clinical medicine, 2020-01, Vol.9 (2), p.370

2020

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Konieczność współpracy Grecji z Turcją w rozwiązaniu kryzysu migracyjnego w Europie

Historia i polityka, 2017-03, Vol.26 (19), p.97-104

Biernacka-Rygiel, Anna

2017

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Low-Molecular-Weight Cyclin E Can Bypass Letrozole-Induced G1 Arrest in Human Breast Cancer Cells and Tumors

Clinical cancer research, 2010-02, Vol.16 (4), p.1179-1190

2010

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Aging and Cardiac Fibrosis

Aging and disease, 2011-04, Vol.2 (2), p.158-173

2011

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Health locus of control as a psychological factor in improving treatment results in adolescents with primary hypertension and diabetes

Health psychology report, 2017-01, Vol.5 (1), p.20-29

2017

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Zarys historii bibliotek parafialnych w Polsce

Archiwa biblioteki i muzea kościelne, 2020-04, Vol.73, p.9-21

2020

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Comprehensive Mapping of Histone Modifications at DNA Double-Strand Breaks Deciphers Repair Pathway Chromatin Signatures

Genome-wide mapping of long-range contacts unveils clustering of DNA double-strand breaks at damaged active genes

Topoisomerase 1 prevents replication stress at R-loop-enriched transcription termination sites

qDSB-Seq is a general method for genome-wide quantification of DNA double-strand breaks using sequencing

Smad3 Signaling Promotes Fibrosis While Preserving Cardiac and Aortic Geometry in Obese Diabetic Mice

Endogenous Thrombospondin 1 Protects the Pressure-Overloaded Myocardium by Modulating Fibroblast Phenotype and Matrix Metabolism

Feasibility Study of a Novel Protease-Activated Fluorescent Imaging System for Real-Time, Intraoperative Detection of Residual Breast Cancer in Breast Conserving Surgery

Wybrane współczesne biblioteki parafialne na terenie dzielnicy Wrocławia - Fabryczna : stan badań na rok 1996/1997

Exposure of Keratinocytes to Candida Albicans in the Context of Atopic Milieu Induces Changes in the Surface Glycosylation Pattern of Small Extracellular Vesicles to Enhance Their Propensity to Interact With Inhibitory Siglec Receptors

Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy

The potential utility of re-mining results of somatic mutation testing: KRAS status in lung adenocarcinoma

Lung adenocarcinomas with isolated TP53 mutation: A comprehensive clinical, cytopathologic and molecular characterization

Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit

Novel de novo mutation affecting two adjacent aminoacids in the EED gene in a patient with Weaver syndrome

Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines

Combined MEK and VEGFR Inhibition in Orthotopic Human Lung Cancer Models Results in Enhanced Inhibition of Tumor Angiogenesis, Growth, and Metastasis

Brain Tissue Low-Level Mosaicism for MTOR Mutation Causes Smith–Kingsmore Phenotype with Recurrent Hypoglycemia—A Novel Phenotype and a Further Proof for Testing of an Affected Tissue

Applications of nanodosimetry in particle therapy planning and beyond

TGF-β signaling in fibrosis

Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes

Konieczność współpracy Grecji z Turcją w rozwiązaniu kryzysu migracyjnego w Europie

Low-Molecular-Weight Cyclin E Can Bypass Letrozole-Induced G1 Arrest in Human Breast Cancer Cells and Tumors

Aging and Cardiac Fibrosis

Health locus of control as a psychological factor in improving treatment results in adolescents with primary hypertension and diabetes

Zarys historii bibliotek parafialnych w Polsce

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