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RAS/MAPK
Publikace
Předměty
Osoby
Publikace
Studium
publication
Mutations in the RAS/MAPK Pathway Drive Replication Repair-Deficient Hypermutated Tumors and Confer Sensitivity to MEK Inhibition
2021 |
2. lékařská fakulta
publication
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
2016 |
2. lékařská fakulta
publication
European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe
2022 |
2. lékařská fakulta
publication
Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey
2022 |
2. lékařská fakulta
publication
Monozygotní dvojčata s Legius syndromem a diferenciální diagnostika Legius syndromu a neurofibromatózy typ 1
2021 |
2. lékařská fakulta
publication
Prenatální fenotyp RASopatií
2020 |
Publikace bez příslušnosti k fakultě
publication
Molekulární patologie cholangiocelulárních nádorů
2019 |
1. lékařská fakulta, 3. lékařská fakulta
publication
Gregor Mendel a řízení růstu dítěte: geny, molekuly a pediatrická klinická praxe
2022 |
2. lékařská fakulta
publication
Integrated Molecular and Clinical Analysis of 1,000 Pediatric Low-Grade Gliomas
2020 |
2. lékařská fakulta
publication
A restricted spectrum of NRAS mutations causes Noonan syndrome
2010 |
2. lékařská fakulta
publication
Novel BRAF mutation in a patient with LEOPARD syndrome and normal intelligence
2009 |
2. lékařská fakulta
publication
Alterations in ALK/ROS1/NTRK/MET drive a group of infantile hemispheric gliomas
2019 |
2. lékařská fakulta
publication
The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered
2021 |
2. lékařská fakulta
publication
An integrative molecular and genomic analysis of pediatric hemispheric low-grade gliomas: an update
2016 |
Ústřední knihovna
publication
Alterations in key signaling pathways in sinonasal tract melanoma. A molecular genetics and immunohistochemical study of 90 cases and comprehensive review of the literature
2022 |
Lékařská fakulta v Plzni
publication
Evidence of novel miR-34a-based therapeutic approaches for multiple myeloma treatment
2017 |
2. lékařská fakulta
publication
13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking
2020 |
2. lékařská fakulta
publication
Combined immunotherapy improves outcome for replication repair deficient (RRD) high-grade glioma failing anti-PD1 monotherapy: A report from the International RRD Consortium
2024 |
2. lékařská fakulta
publication
A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature
2016 |
2. lékařská fakulta, 1. lékařská fakulta, Fakulta tělesné výchovy a sportu
publication
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay
2018 |
2. lékařská fakulta, 1. lékařská fakulta