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pro vyhledávání: '"Marušić, Maruška"'
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Autor:
Grizelj, Danijela, Marušić, Maruška, Ajduk, Marko, Pavić, Predrag, Jakšić, Ozren, Pandžić Jakšić, Vlatka
Povezanost izražaja omentina u masnom tkivu vrata i metaboličkih rizičnih čimbenika u bolesnika s endarterektomijom karotidnih arteija
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::1394c2474596b958434e964601602b53
https://www.bib.irb.hr/736354
https://www.bib.irb.hr/736354
Autor:
Marušić, Maruška, Livun, Ana, Pejša, Senčica, Hariš, Višnja, Jakšić, Ozren, Mitrović, Zdravko, Piršić, Mario, Prka, Željko, Štoos-Veić, Tajana, Tomasović, Čedna, Kušec, Rajko
Cilj: Analiza 1849G>T mutacije u JAK2 (kodira za JAK2V617F) dio je rutinske dijagnostike MPN. Kvantifikacija mutiranog alela sve se više koristi za praćenje odgovora na terapiju. Iz krvi 10 bolesnika izolirana je DNA. Metodom kvantitativnog PCR odr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::5810a1520f856030d47a8d2b09a417b9
https://www.bib.irb.hr/692333
https://www.bib.irb.hr/692333
Autor:
Pallisgaard, Niels, Hasselbach, Hans Carl, Cassinat, A., Kjaer, Lars, Vorland, M., Dicker, F., Bellosillo, Beatriz, Kristensen, T., Andersen, M., Lippert, Eric, Schwarz, Jiri, Bryon, J., Naguib, D., Nomdedeu, J., Aggerholm, A., Wojtaszewska, Marzena, Andrikovics, H, Marušić, Maruška, Ayala, R, Leibundgut, E, Samuelson, E, Lode, L, Girodon, F, Percy, Melanie, Hermouet, Sylvie
Background: Analysis for the 1849G>T mutation in JAK2 (encoding JAK2- V617F) is routine in the diagnosis of myeloproliferative neoplasms (MPNs). The quantification of the allelic burden in JAK2- V617F positive patients is increasingly used to monitor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::6ca74caf1fc8f7c4aafb2f089bec346c
https://www.bib.irb.hr/674200
https://www.bib.irb.hr/674200
Autor:
Kjaer, Lasse, Lippert, Eric, Girdon, Francois, Schnittger, Susanne, Carillo, Serge, Hasselbach Riley, Caroline, Bellosillo, Beatriz, Westman, Maj, Weis Bjerrum, Ole, Wojataszewska, Marzena, Kielsgaard Kristensen, Thomas, Percy, Melanie, McMullin, Mary Francis, Marušić, Maruška, Rosmond, Caroline, Palmquist, Lars, Hermouet, Sylvie, Hasselbach, Hans
A subset of PV patients harbor mutations in a discrete region of exon 12 in the JAK2 gene. As these mutations are fairly rare, only a few studies have attempted to describe how they reflect disease development and their utility as a prognostic marker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::bf0d764e51ca4633abfe5a93abf06920
https://www.bib.irb.hr/651087
https://www.bib.irb.hr/651087
Autor:
Kjaer, Lasse, Lippert, Eric, Girdon, Francois, Schnittger, Susanne, Carillo, Serge, Hasselbach Riley, Caroline, Bellosillo, Beatriz, Westman, Maj, Weis Bjerrum, Ole, Wojataszewska, Marzena, Kielsgaard Kristensen, Thomas, Percy, Melanie, McMullin, Mary Francis, Marušić, Maruška, Rosmond, Caroline, Palmquist, Lars, Hermouet, Sylvie, Hasselbach, Hans
A subset of polycythemia vera (PV) patients harbor mutations in a discrete region of exon 12 in the JAK2 gene. So far more than 40 individual mutations have been described involving amino acids 533 to 547 including substitutions, deletions, and dupli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::54b02cf57c919ecd35b89c0bd3a1f4d7
https://www.bib.irb.hr/674157
https://www.bib.irb.hr/674157
Autor:
Marijanović, Inga, Vrsalović Marušić, Maruška, Mihalić Caput, Katarina, Matić, Igor, Antunović, Maja, Kušec, Rajko, Nagy, Biserka
Myeloproliferative diseases present the group of clonal malignant diseases of hematopoietic stem cell. Somatic mutation of JAK2 gene (JAK2V617F+) is present in most of the patients (>90%) with polycythemia vera (PV), and 50% of patients with essentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::647b062fed2e696fdfa6825ea0ac9192
https://www.bib.irb.hr/526769
https://www.bib.irb.hr/526769
Autor:
Vrsalovic-Marušić, Maruška, Pejša, Vlatko, Vejic-Stoos, Tajana, Kolonic-Ostojic, Slobodanka, Ajdukovic, Radmila, Haris, Visnja, Jaksic, Ozren, Kusec, Rajko
Discovery of V617F mutation in JAK2 tyrosine kinase gene in myeloid progenitors provided new insight into the pathogenesis and clinical understanding of CMPD. There are several lines of evidence suggesting the existence of local hematopoietic bone ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a187ed5e7da20775064b485246ad3392
https://www.bib.irb.hr/323536
https://www.bib.irb.hr/323536
Sažetak će biti upisan naknadno.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::c29b65b1cc7bfd77f9869220becf0433
https://www.bib.irb.hr/75781
https://www.bib.irb.hr/75781
Autor:
Marušić, Maruška, Kardum-Skelin, Ika, Dominis, Mara, Pejša, Vlatko, Ajduković, Marina, Boranić, Milivoj, Kušec, Rajko
The myelodysplastic syndrome (MDS) comprises a heterogeneous group of clonal bone marrow disorders characterized by abnormal differentiation and maturation of myeloid cells, bone marrow failure and a genetic instability with enhaced risk to transform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::629640fd28faa42b4f6924a3570bed2a
https://www.bib.irb.hr/75780
https://www.bib.irb.hr/75780