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Maciej Dabrowski
Maciej Dabrowski
CruxBio
Zweryfikowany adres z cruxbio.eu
Tytuł
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Translational readthrough potential of natural termination codons in eucaryotes–The impact of RNA sequence
M Dabrowski, Z Bukowy-Bieryllo, E Zietkiewicz
RNA biology 12 (9), 950-958, 2015
2112015
Advances in therapeutic use of a drug-stimulated translational readthrough of premature termination codons
M Dabrowski, Z Bukowy-Bieryllo, E Zietkiewicz
Molecular medicine 24, 1-15, 2018
1332018
Arabidopsis protein phosphatase 2C ABI1 interacts with type I ACC synthases and is involved in the regulation of ozone-induced ethylene biosynthesis
SJ Ludwików A, Cieśla A, Kasprowicz-Maluśki A, Mituła F, Tajdel M, Gałgański ...
Mol Plant., 960-76, 2014
802014
Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia
Z Bukowy-Bieryllo, M Dabrowski, M Witt, E Zietkiewicz
RNA biology 13 (10), 1041-1050, 2016
432016
Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms
Z Bukowy-Bieryllo, A Rabiasz, M Dabrowski, A Pogorzelski, A Wojda, ...
Journal of Medical Genetics 56 (11), 769-777, 2019
392019
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative
G Butler-Laporte, G Povysil, JA Kosmicki, ET Cirulli, T Drivas, S Furini, ...
Plos Genetics 18 (11), e1010367, 2022
262022
The Thousand Polish Genomes—A Database of Polish Variant Allele Frequencies
E Kaja, A Lejman, D Sielski, M Sypniewski, T Gambin, M Dawidziuk, ...
International Journal of Molecular Sciences 23 (9), 4532, 2022
192022
Properties of Non-Aminoglycoside Compounds Used to Stimulate Translational Readthrough of PTC Mutations in Primary Ciliary Dyskinesia
M Dabrowski, Z Bukowy-Bieryllo, CL Jackson, E Zietkiewicz
International Journal of Molecular Sciences 22 (9), 4923, 2021
132021
Proceedings of the 4 th BEAT-PCD Conference and 5 th PCD Training School
LE Gardner, KL Horton, A Shoemark, JS Lucas, KG Nielsen, ...
BMC Proceedings 14 (8), 1-17, 2020
42020
SARS-CoV-2 infection activating a novel variant of the NOTCH3 gene and subsequently causing development of CADASIL
ZJ Król, M Dorobek, M Dąbrowski, J Zielińska-Turek, B Mruk, J Walecki, ...
Archives of Medical Science, 2022
32022
Validation of HER2 Status in Whole Genome Sequencing Data of Breast Cancers with the Ploidy-Corrected Copy Number Approach
M Wojtaszewska, R Stępień, A Woźna, M Piernik, P Sztromwasser, ...
Molecular Diagnosis & Therapy, 1-12, 2022
22022
Gene Variants Related to Cardiovascular and Pulmonary Diseases May Correlate with Severe Outcome of COVID-19
M Sypniewski, ZJ Król, J Szyda, E Kaja, M Mroczek, T Suchocki, A Lejman, ...
International Journal of Molecular Sciences 23 (15), 8696, 2022
12022
The cancer-risk variant frequency among Polish population reported by the first national whole-genome sequencing study
M Mroczek, J Liu, M Sypniewski, T Pieńkowski, B Itrych, J Stojak, ...
Frontiers in Oncology 13, 1045817, 2023
2023
Improved response prediction to immune checkpoint inhibitors by combining TMB and WGS-driven genomic features in NSCLC
PZ Nawrocka-Muszyńska, K. Pacewicz, M. Mędzin, P. Sztromwasser, M. Dabrowski ...
Annals of Oncology 33, S448-S554, 2022
2022
Validation of HER2 status in whole genome sequencing data of breast cancers with AI-driven, ploidy-corrected approach
W Marzena, S Rafał, W Alicja, P Maciej, D Maciej, G Michał, S Sławomir, ...
medRxiv, 2021.08. 30.21258379, 2021
2021
Personalized medicine in advanced breast cancer: AI-driven genomic test for CDK4/6 treatment response prediction
P Zawadzki, A Woźna, P Sztromwasser, W Majer-Burman, R Stępień, ...
Annals of Oncology 32, S925, 2021
2021
Innowacje w diagnostyce nowotworów: genomika, sekwencjonowanie nowej generacji i sztuczna inteligencja
M Wojtaszewska, M Dąbrowski
NOWOCZESNA DIAGNOSTYKA W ONKOLOGII, 56-78, 2021
2021
Stymulowany aminoglikozydami translacyjny odczyt przedwczesnych kodonów STOP w wybranych genach zaangażowanych w patogenezę pierwotnej dyskinezy rzęsek (PCD)
M Dabrowski
Instytut Genetyki Człowieka Polskiej Akademii Nauk , 978-83-950393-0-0, 2018
2018
Primary ciliary dyskinesia in the Polish population – from understanding the genetic basis to introduction of personalized therapy.
Z Bukowy-Bieryłło, K Voelkel, M Dąbrowski, E Rutkiewicz, P Daca-Roszak, ...
Annual Report Polish Academy of Sciences, 66-68, 2017
2017
Motile cilia disorders and approaches to their treatment
M Witt, E Ziętkiewicz, Z Bukowy-Bieryłło, M Dąbrowski
Acta Biochemica Polonica, 2014
2014
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