Zobrazeno 1 - 10
of 971
pro vyhledávání: '"E Van Hul"'
Autor:
Pinitchun, Chalisa1,2,3 (AUTHOR) chalisap16@hotmail.com, Panpetch, Wimonrat4 (AUTHOR), Bhunyakarnjanarat, Thansita1,2 (AUTHOR), Udompornpitak, Kanyarat1,2 (AUTHOR), Do, Huy Thanh1 (AUTHOR), Visitchanakun, Peerapat1,2 (AUTHOR), Wannigama, Dhammika Leshan2,5,6,7,8,9 (AUTHOR), Udomkarnjananun, Suwasin10 (AUTHOR), Sukprasansap, Monruedee11 (AUTHOR), Tencomnao, Tewin12,13 (AUTHOR), Tangtanatakul, Pattarin1,2,3 (AUTHOR), Leelahavanichkul, Asada1,2,4 (AUTHOR) aleelahavanit@gmail.com
Publikováno v:
PLoS ONE. 10/18/2024, Vol. 19 Issue 10, p1-24. 24p.
Autor:
Oh, Shin Ae1,2 (AUTHOR), Jeon, Jiyeon1,2 (AUTHOR), Je, Su-yeon1,2 (AUTHOR), Kim, Seoyoung1,2 (AUTHOR), Jung, Joohyun1 (AUTHOR), Ko, Hyuk Wan1 (AUTHOR) kohw@yonsei.ac.kr
Publikováno v:
Cell Communication & Signaling. 10/9/2024, Vol. 22 Issue 1, p1-11. 11p.
Publikováno v:
Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu. 9/28/2024, Vol. 28 Issue 27, p4319-4324. 6p.
Autor:
Zhang, Rong1,2,3 (AUTHOR), Mu, Xiaodan4 (AUTHOR), Liu, Dawei2,5 (AUTHOR), Chen, Chider2 (AUTHOR), Meng, Bowen6 (AUTHOR), Qu, Yan6 (AUTHOR), Liu, Jin2,7 (AUTHOR), Wang, Runci2 (AUTHOR), Li, Chuanjie1 (AUTHOR), Mao, Xueli2,6 (AUTHOR), Wang, Qintao8 (AUTHOR) wangqintao@aliyun.com, Zhang, Qingbin1 (AUTHOR) qingbinzhang@gzhmu.edu.cn
Publikováno v:
Journal of Nanobiotechnology. 9/20/2024, Vol. 22 Issue 1, p1-21. 21p.
Autor:
Hipps, Daniel1,2 (AUTHOR) daniel.hipps@nhs.net, Pyle, Angela2 (AUTHOR), Porter, Anna L. R.2 (AUTHOR), Dobson, Philip F.1,2 (AUTHOR), Tuppen, Helen2 (AUTHOR), Lawless, Conor2 (AUTHOR), Russell, Oliver M.2 (AUTHOR), Turnbull, Doug M.1,2 (AUTHOR), Deehan, David J.1 (AUTHOR), Hudson, Gavin3 (AUTHOR) gavin.hudson@ncl.ac.uk
Publikováno v:
Scientific Reports. 9/9/2024, Vol. 14 Issue 1, p1-10. 10p.
Autor:
Moreno, Caren N.1 (NURSE) carenmoreno28@gmail.com, Gomez, Jorge N.1 (NURSE) nicolasgoib@gmail.com, Taranto, María P.2 (AUTHOR) ptaranto@cerela.org.ar, Ledesma, Ana E.1,3 (NURSE) ana1ledesma@yahoo.com.ar, Bustos, Ana Y.1,4,5 (NURSE) abustos@uspt.edu.ar
Publikováno v:
BioTech. Sep2024, Vol. 13 Issue 3, p29. 14p.
Autor:
Martin Ebeling, C Lacza, Klaus Lindpaintner, P Hildering, Wim Wuyts, M Dioszegi, B Vickery, Patrick Willems, Wendy Balemans, Dorothee Foernzler, E Van Hul, W. Van Hul, N Patel, Jbgm Verheij, Frederik G. Dikkers
Publikováno v:
JOURNAL OF MEDICAL GENETICS, 39(2), 91-97. BMJ PUBLISHING GROUP
Journal of medical genetics
Journal of medical genetics
Van Buchem disease is an autosomal recessive skeletal dysplasia characterised by generalised bone overgrowth, predominantly in the skull and mandible. Clinical complications including facial nerve palsy, optic atrophy, and impaired hearing occur in m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a90e42c64ee715f5e021c0ef0a7b47b6
https://doi.org/10.1136/jmg.39.2.91
https://doi.org/10.1136/jmg.39.2.91
Publikováno v:
Bone
X-linked calvarial hyperostosis is a rare disorder characterized by isolated calvarial thickening. Symptoms are prominent frontoparietal bones, a flat nasal root and a short upturned nose, a high forehead with ridging of the metopic and sagittal sutu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4408fdc3548eb928f04108f77c3a875
https://hdl.handle.net/10067/1288940151162165141
https://hdl.handle.net/10067/1288940151162165141
Autor:
S. Bahabri, Andrea Superti-Furga, Jamil Al-Alami, J K Herd, W. Van Hul, Jean Roudier, H Rezai-Delui, M. Le Merrer, Wafaa M. Suwairi, J R Hurvitz, D Holderbaum, Hatem El-Shanti, Richard M. Pauli, Eric Legius, E Van Hul, Matthew L. Warman
Publikováno v:
Nature genetics
Members of the CCN (for CTGF, cyr61/cef10, nov) gene family encode cysteine-rich secreted proteins with roles in cell growth and differentiation1. Cell-specific and tissue-specific differences in the expression and function of different CCN family me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e342bc514bf910e0789dfac790954430
https://doi.org/10.1038/12699
https://doi.org/10.1038/12699
Autor:
P. Bossuyt, A. M. W. Van Den Ouweland, D. J. J. Halley, W. Van Hul, L Vits, Jan Wauters, K. De Boulle, Paul Coucke, M. Nemtsova, Wim Wuyts, P. J. Willems, Thomas B. Shows, Edwin Reyniers, Norma J. Nowak, B. B. A. De Vries, L. Mallet, Wendy Balemans, Julie McGaughran, I. Herrygers, E Van Hul, Jan Hendrickx, Erik Fransen
Publikováno v:
Human molecular genetics
Scopus-Elsevier
Scopus-Elsevier
Hereditary multiple exostosis (EXT) is an autosomal dominant condition mainly characterized by the presence of multiple exostoses on the long bones. These exostoses are benign cartilaginous tumors (enchondromata). Three different EXT loci on chromoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::214367ee36871099d37f2605314814e0
https://doi.org/10.1093/hmg/5.10.1547
https://doi.org/10.1093/hmg/5.10.1547