Denisa Hathazi
Denisa Hathazi
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JAK inhibitor improves type I interferon induced damage: proof of concept in dermatomyositis
L Ladislau, X Suárez-Calvet, S Toquet, O Landon-Cardinal, D Amelin, ...
Brain 141 (6), 1609-1621, 2018
Associative chemosensing by fluorescent macrocycle–dye complexes–a versatile enzyme assay platform beyond indicator displacement
F Biedermann, D Hathazi, WM Nau
Chemical Communications 51 (24), 4977-4980, 2015
Mutations in INPP5K, encoding a phosphoinositide 5-phosphatase, cause congenital muscular dystrophy with cataracts and mild cognitive impairment
M Wiessner, A Roos, CJ Munn, R Viswanathan, T Whyte, D Cox, ...
The American Journal of Human Genetics 100 (3), 523-536, 2017
Oxidative protection of hemoglobin and hemerythrin by cross-linking with a nonheme iron peroxidase: potentially improved oxygen carriers for use in blood substitutes
D Hathazi, AC Mot, A Vaida, F Scurtu, I Lupan, E Fischer-Fodor, ...
Biomacromolecules 15 (5), 1920-1927, 2014
Clinical presentation and proteomic signature of patients with TANGO2 mutations
N Mingirulli, A Pyle, D Hathazi, CL Alston, N Kohlschmidt, G O'Grady, ...
Journal of inherited metabolic disease 43 (2), 297-308, 2020
Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency
D Hathazi, H Griffin, MJ Jennings, M Giunta, C Powell, SF Pearce, ...
The EMBO journal 39 (23), e105364, 2020
Comparative In Vivo Effects of Hemoglobin-Based Oxygen Carriers (HBOC) with Varying Prooxidant and Physiological Reactivity
VA Toma, AD Farcaș, I Roman, B Sevastre, D Hathazi, F Scurtu, ...
PLoS One 11 (4), e0153909, 2016
The reaction of oxy hemoglobin with nitrite: Mechanism, antioxidant-modulated effect, and implications for blood substitute evaluation
D Hathazi, F Scurtu, C Bischin, A Mot, AAA Attia, J Kongsted, ...
Molecules 23 (2), 350, 2018
Biochemical and pathological changes result from mutated Caveolin-3 in muscle
JA González Coraspe, J Weis, ME Anderson, U Münchberg, K Lorenz, ...
Skeletal muscle 8 (1), 1-19, 2018
In-depth phenotyping of lymphoblastoid cells suggests selective cellular vulnerability in Marinesco-Sjögren syndrome
L Kollipara, S Buchkremer, JAG Coraspe, D Hathazi, J Senderek, J Weis, ...
Oncotarget 8 (40), 68493, 2017
GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice
Y Issop, D Hathazi, MM Khan, R Rudolf, J Weis, S Spendiff, CR Slater, ...
Human molecular genetics 27 (18), 3218-3232, 2018
Proteomic profiling unravels a key role of specific macrophage subtypes in sporadic inclusion body myositis
A Roos, C Preusse, D Hathazi, HH Goebel, W Stenzel
Frontiers in Immunology 10, 1040, 2019
Identification of candidate protein markers in skeletal muscle of laminin-211-deficient CMD type 1A-patients
H Kölbel, D Hathazi, M Jennings, R Horvath, A Roos, U Schara
Frontiers in Neurology 10, 470, 2019
SIL1 deficiency causes degenerative changes of peripheral nerves and neuromuscular junctions in fish, mice and human
V Phan, D Cox, S Cipriani, S Spendiff, S Buchkremer, E O'Connor, ...
Neurobiology of Disease 124, 218-229, 2019
Involvement of ferryl in the reaction between nitrite and the oxy forms of globins
D Hathazi, SD Mahuţ, FV Scurtu, C Bischin, C Stanciu, AA Attia, G Damian, ...
JBIC Journal of Biological Inorganic Chemistry 19 (7), 1233-1239, 2014
Immunofluorescence-based analysis of Caveolin-3 in the diagnostic Management of Neuromuscular Diseases
A Roos, D Hathazi, U Schara
Caveolae, 197-216, 2020
In vivo evaluation of hemerythrin-based oxygen carriers: Similarities with hemoglobin-based counterparts
VA Toma, AD Farcas, I Roman, B Sevastre, D Hathazi, F Scurtu, ...
International journal of biological macromolecules 107, 1422-1427, 2018
NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and mice
MJ Jennings, A Kagiava, L Vendredy, EL Spaulding, M Stavrou, ...
Brain, 2022
Identification of cellular pathogenicity markers for SIL1 mutations linked to marinesco-sjögren syndrome
C Gatz, D Hathazi, U Münchberg, S Buchkremer, T Labisch, B Munro, ...
Frontiers in Neurology 10, 562, 2019
INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH
D Hathazi, D Cox, A d'Amico, G Tasca, R Charlton, RY Carlier, ...
Brain 144 (8), 2427-2442, 2021
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