Research Explorer

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Researcher

Igor Fijalkowski

17 Results

2022

Hidden in plain sight : challenges in proteomics detection of small ORF-encoded polypeptides

Igor FijalkowskiPatrick WillemsVeronique JonckheereLaure SimoensPetra Van Damme

A2 Journal Article in MICROLIFE

Oncogenic deubiquitination controls tyrosine kinase signaling and therapy response in acute lymphoblastic leukemia

Qi JinBlanca Gutierrez DiazTim PietersYalu ZhouSonali NarangIgor FijalkowskiCristina BorinJolien Van LaereMonique PaytonByoung-Kyu Cho et al.

A1 Journal Article in SCIENCE ADVANCES

Selective ribosome profiling reveals a role for SecB in the co-translational inner membrane protein biogenesis

Lena EismannIgor FijalkowskiCarla Verónica GalmozziJiří KoubekFrank TippmannPetra Van DammeGünter Kramer

A1 Journal Article in CELL REPORTS

Splicing dysregulation in human hematologic malignancies : beyond splicing mutations

Jonas De KeselIgor FijalkowskiJustin TaylorPanagiotis Ntziachristos

A1 Journal Article in TRENDS IN IMMUNOLOGY

2021

Capturing salmonella SspH2 host targets in virus-like particles

Margaux De MeyerIgor FijalkowskiVeronique JonckheereDelphine De SutterSven EyckermanPetra Van Damme

A1 Journal Article in FRONTIERS IN MEDICINE

Small protein enrichment improves proteomics detection of sORF encoded polypeptides

Igor FijalkowskiMarlies PeetersPetra Van Damme

A1 Journal Article in FRONTIERS IN GENETICS

2020

Bacterial riboproteogenomics : the era of N-terminal proteoform existence revealed

Daria FijalkowskaIgor FijalkowskiPatrick WillemsPetra Van Damme

A1 Journal Article in FEMS MICROBIOLOGY REVIEWS

Lost and found : re-searching and re-scoring proteomics data aids genome annotation and improves proteome coverage

Patrick WillemsIgor FijalkowskiPetra Van Damme

A1 Journal Article in MSYSTEMS

2017

The Lrp4R1170Q homozygous knock-in mouse recapitulates the bone phenotype of sclerosteosis in humans

E BoudinT YorganIgor FijalkowskiS SonntagE SteenackersG HendrickxS PeetersA De MaréB VervaetA Verhulst et al.

A1 Journal Article in JOURNAL OF BONE AND MINERAL RESEARCH

2016

A novel domain-specific mutation in a sclerosteosis patient suggests a role of LRP4 as an anchor for sclerostin in human bone

Igor FijalkowskiE GeetsE SteenackersV Van HoofFJ RamosG MortierAM FortunaW Van HulE Boudin

A1 Journal Article in JOURNAL OF BONE AND MINERAL RESEARCH

Eight mutations including 5 novel ones in the COL1A1 gene in Czech patients with osteogenesis imperfecta

L HruskovaIgor FijalkowskiW Van HulI MarikG MortierP MartasekI Mazura

A1 Journal Article in BIOMEDICAL PAPERS - OLOMOUC

Further delineation of facioaudiosymphalangism syndrome : description of a family with a novel NOG mutation and without hearing loss

A BayatIgor FijalkowskiT AndersenSA AbdulmunemJ van den EndeW Van Hul

A1 Journal Article in AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genetic control of bone mass

E BoudinIgor FijalkowskiG HendrickxW Van Hul

A1 Journal Article in MOLECULAR AND CELLULAR ENDOCRINOLOGY

2014

Sclerosing bone dysplasias : leads toward novel osteoporosis treatments

Igor FijalkowskiE BoudinG MortierW Van Hul

A1 Journal Article in CURRENT OSTEOPOROSIS REPORTS

Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters

G HendrickxE BoudinIgor FijalkowskiTL NielsenM AndersenK BrixenW Van Hul

A1 Journal Article in BONE

2013

Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis

E BoudinE PitersIgor FijalkowskiG StevenheydensE SteenackersO KuisminJS MoilanenG MortierW Van Hul

A1 Journal Article in BONE

The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases

E BoudinIgor FijalkowskiE PitersW Van Hul

A1 Journal Article in SEMINARS IN ARTHRITIS AND RHEUMATISM