Publication Records

POOVAKULATHU ABRAHAM, Sara, Alexandru NITĂ, Pavel KREJČÍ and Michaela BOSÁKOVÁ. Cilia kinases in skeletal development and homeostasis. Developmental dynamics. United States: Wiley-Liss, 2022, vol. 251, No 4, p. 577-608. ISSN 1058-8388. Available from: https://dx.doi.org/10.1002/dvdy.426.

KIMURA, T., Michaela BOSÁKOVÁ, Y. NONAKA, Eva HRUBA, K. YASUDA, S. FUTAKAWA, T. KUBOTA, Bohumil FAFÍLEK, Tomáš GREGOR, Sara POOVAKULATHU ABRAHAM, Regína GOMOLKOVÁ, Silvie BELASKOVA, Martin PEŠL, F. CSUKASI, I. DURAN, M. FUJIWARA, Michaela KAVKOVA, Tomas ZIKMUND, Josef KAISER, Marcela BUCHTOVÁ, D. KRAKOW, Y. NAKAMURA, K. OZONO and Pavel KREJČÍ. An RNA aptamer restores defective bone growth in FGFR3-related skeletal dysplasia in mice. Science Translational Medicine. Washington: American Association for the Advancement of Science, 2021, vol. 13, No 592, p. "eaba4226", 14 pp. ISSN 1946-6234. Available from: https://dx.doi.org/10.1126/scitranslmed.aba4226.

NITA, Alexandru, Sara POOVAKULATHU ABRAHAM, Pavel KREJČÍ and Michaela BOSÁKOVÁ. Oncogenic FGFR Fusions Produce Centrosome and Cilia Defects by Ectopic Signaling. Cells. Basel: MDPI, 2021, vol. 10, No 6, p. 1-25. ISSN 2073-4409. Available from: https://dx.doi.org/10.3390/cells10061445.

GREGOR, Tomáš, Michaela BOSÁKOVÁ, Alexandru NITĂ, Sara POOVAKULATHU ABRAHAM, Bohumil FAFÍLEK, Nicole ČERNOHORSKÁ, Jan RYNEŠ, Silvie TRANTÍRKOVÁ, Daniela ŽÁČKOVÁ, Jiří MAYER, Lukáš TRANTÍREK and Pavel KREJČÍ. Elucidation of protein interactions necessary for the maintenance of the BCR-ABL signaling complex. Cellular and molecular life sciences. BASEL: SPRINGER BASEL AG, 2020, vol. 77, No 19, p. 3885-3903. ISSN 1420-682X. Available from: https://dx.doi.org/10.1007/s00018-019-03397-7.

BOSÁKOVÁ, Michaela, Sara POOVAKULATHU ABRAHAM, Alexandru NITĂ, Eva HRUBA, Marcela BUCHTOVA, S. Paige TAYLOR, Ivan DURAN, Jorge MARTIN, Kateřina SVOZILOVÁ, Tomáš BÁRTA, Miroslav VAŘECHA, Lukáš BÁLEK, Jiri KOHOUTEK, Tomasz Witold RADASZKIEWICZ, Ganesh V. PUSAPATI, Vítězslav BRYJA, Eric T. RUSH, Isabelle THIFFAULT, Deborah A. NICKERSON, Michael J. BAMSHAD, Rajat ROHATGI, Daniel H. COHN, Deborah KRAKOW and Pavel KREJČÍ. Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signaling. EMBO MOLECULAR MEDICINE. HOBOKEN: WILEY-BLACKWELL, 2020, vol. 12, No 11, p. 1-20. ISSN 1757-4676. Available from: https://dx.doi.org/10.15252/emmm.201911739.

BOSÁKOVÁ, Michaela, Alexandru NITĂ, Tomáš GREGOR, Miroslav VAŘECHA, Iva GUDERNOVÁ, Bohumil FAFÍLEK, Tomáš BÁRTA, Neha BASHEER, Sara POOVAKULATHU ABRAHAM, Lukáš BÁLEK, Markéta TOMANOVÁ, Jana FIALOVÁ KUČEROVÁ, Juraj BOSÁK, David POTĚŠIL, Jennifer ZIEBA, Jieun SONG, Peter KONIK, Sohyun PARK, Ivan DURAN, Zbyněk ZDRÁHAL, David ŠMAJS, Gert JANSEN, Zheng FU, Hyuk Wan KO, Aleš HAMPL, Lukáš TRANTÍREK, Deborah KRAKOW and Pavel KREJČÍ. Fibroblast growth factor receptor influences primary cilium length through an interaction with intestinal cell kinase. Proceedings of the National Academy of Sciences of the United States of America. WASHINGTON: NATL ACAD SCIENCES, 2019, vol. 116, No 10, p. 4316-4325. ISSN 0027-8424. Available from: https://dx.doi.org/10.1073/pnas.1800338116.