Zobrazeno 1 - 10
of 403
pro vyhledávání: '"Kazuyuki Sugahara"'
Autor:
Wing Lee Chan, Magdalena Steiner, Tomasz Witkos, Johannes Egerer, Björn Busse, Shuji Mizumoto, Jan M Pestka, Haikuo Zhang, Ingrid Hausser, Layal Abo Khayal, Claus-Eric Ott, Mateusz Kolanczyk, Bettina Willie, Thorsten Schinke, Chiara Paganini, Antonio Rossi, Kazuyuki Sugahara, Michael Amling, Petra Knaus, Danny Chan, Martin Lowe, Stefan Mundlos, Uwe Kornak
Publikováno v:
PLoS Genetics, Vol 14, Iss 3, p e1007242 (2018)
Gerodermia osteodysplastica (GO) is characterized by skin laxity and early-onset osteoporosis. GORAB, the responsible disease gene, encodes a small Golgi protein of poorly characterized function. To circumvent neonatal lethality of the GorabNull full
Externí odkaz:
https://doaj.org/article/d57661c1748c402db63c5dbeb8b9b7d0
Publikováno v:
Molecules, Vol 20, Iss 3, Pp 3527-3548 (2015)
With recent advances in the construction of synthetic glycans, selective targeting of the extracellular matrix (ECM) as a potential treatment for a wide range of diseases has become increasingly popular. The use of compounds that mimic the structure
Externí odkaz:
https://doaj.org/article/8e1b58d55ae34f699e1ab235649335ca
Autor:
Kenji Suzuki, Somasundaram Arumugam, Junji Yokoyama, Yusuke Kawauchi, Yutaka Honda, Hiroki Sato, Yutaka Aoyagi, Shuji Terai, Kazuichi Okazaki, Yasuo Suzuki, Shuji Mizumoto, Kazuyuki Sugahara, Raja Atreya, Markus F Neurath, Kenichi Watanabe, Taishi Hashiguchi, Hiroyuki Yoneyama, Hitoshi Asakura
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0158967 (2016)
Induction of mucosal healing (MH) is an important treatment goal in inflammatory bowel disease (IBD). Although the molecular mechanisms underlying MH in IBD is not fully explored, local fibrosis would contribute to interfere mucosal repair. Carbohydr
Externí odkaz:
https://doaj.org/article/bdc39cdabfa94c89bba24d1bfc1d6290
Publikováno v:
Encyclopedia of Marine Biotechnology
Publikováno v:
Biomolecules, Vol 2, Iss 4, Pp 549-563 (2012)
Chondroitin sulfate (CS) chains are involved in the regulation of various biological processes. However, the mechanism underlying the catabolism of CS is not well understood. Hyaluronan (HA)-degrading enzymes, the hyaluronidases, are assumed to act a
Externí odkaz:
https://doaj.org/article/8e94d2c40b28475b9d70a24f6bfa4778
Publikováno v:
Pharmaceuticals, Vol 10, Iss 2, p 34 (2017)
The indispensable roles of dermatan sulfate-proteoglycans (DS-PGs) have been demonstrated in various biological events including construction of the extracellular matrix and cell signaling through interactions with collagen and transforming growth fa
Externí odkaz:
https://doaj.org/article/037fcdc379f5493cacd5226b53c770cf
Autor:
Yuya, Hirata, Kazuyuki, Sugahara, Hiroki, Hanaiwa, Yumiko, Funashima, Kenichi, Sato, Zenzo, Nagasawa, Tsukuru, Umemura
Publikováno v:
Rinsho Biseibutsu Jinsoku Shindan Kenkyukai shi = JARMAM : Journal of the Association for Rapid Method and Automation in Microbiology. 29(2)
Genetic testing is widely used as a rapid diagnostic method to identify microorganisms and detect antibiotic resistance genes. The nucleic acid to be analyzed is located inside the cell wall, the cell membrane or nuclear envelope. Therefore, it is es
Autor:
Susanne Greber-Platzer, Nicholas Katsanis, Marie T. McDonald, Andrea Superti-Furga, Kazuyuki Sugahara, Azita Sadeghpour, Sheila Unger, Shuji Mizumoto, Shuhei Yamada, Gundula Povysil, Erica E. Davis, Andreas R. Janecke, Kristen L. Deak, Julia Vodopiutz
Publikováno v:
Human mutation, vol. 41, no. 3, pp. 655-667
Human Mutation
Human Mutation
Congenital disorders of glycosylation (CDGs) comprise a large number of inherited metabolic defects that affect the biosynthesis and attachment of glycans. CDGs manifest as a broad spectrum of disease, most often including neurodevelopmental and skel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbedb42bb51947847e8b5ad0946ac2c2
https://serval.unil.ch/resource/serval:BIB_CED95552EEA3.P001/REF.pdf
https://serval.unil.ch/resource/serval:BIB_CED95552EEA3.P001/REF.pdf
Autor:
José L. Neira, Cédric Przybylski, Kazuyuki Sugahara, Fuchuan Li, Régis Daniel, Runmiao Jiao, Wenshuang Wang, Liran Shi, Cai Xiaojuan, Chrystel Lopin-Bon
Publikováno v:
Biochemical Journal
Biochemical Journal, 2020, 478 (2), pp.281-298. ⟨10.1042/BCJ20200657⟩
Biochemical Journal, Portland Press, 2020, 478 (2), pp.281-298. ⟨10.1042/BCJ20200657⟩
Biochemical Journal, 2020, 478 (2), pp.281-298. ⟨10.1042/BCJ20200657⟩
Biochemical Journal, Portland Press, 2020, 478 (2), pp.281-298. ⟨10.1042/BCJ20200657⟩
International audience; Recently, a novel CS/DS 4-O-endosulfatase was identified from a marine bacterium and its catalytic mechanism was investigated further (Wang, W., et. al (2015) J. Biol. Chem.290, 7823–7832; Wang, S., et. al (2019) Front. Micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d46ef2774c5e2bd7962bd00b53dae66c
https://univ-evry.hal.science/hal-03098070
https://univ-evry.hal.science/hal-03098070
Autor:
Hamish S. Scott, Ravi Savarirayan, Alicia B. Byrne, Milena Babic, Kazuyuki Sugahara, Jan Liebelt, Lynette Moore, Gen Nishimura, Hatice Mutlu-Albayrak, Shuji Mizumoto, Shuhei Yamada, Sarah L King-Smith, Peer Arts, Christopher P. Barnett, Andreas W. Schreiber, Patrick Yap, Jinghua Feng
Publikováno v:
Journal of Medical Genetics
BackgroundPseudodiastrophic dysplasia (PDD) is a severe skeletal dysplasia associated with prenatal manifestation and early lethality. Clinically, PDD is classified as a ‘dysplasia with multiple joint dislocations’; however, the molecular aetiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3060e1cde1815b5019faeea0309f7354
https://hdl.handle.net/11541.2/141568
https://hdl.handle.net/11541.2/141568