Zobrazeno 1 - 9 of 9 pro vyhledávání: '"T H van Kuppevelt"'
1
Akademický článek
Differential binding of chemokines CXCL1, CXCL2 and CCL2 to mouse glomerular endothelial cells reveals specificity for distinct heparan sulfate domains.
Autor: J J van Gemst, M Kouwenberg, A L W M M Rops, T H van Kuppevelt, J H Berden, T J Rabelink, M A Loeven, J van der Vlag
Publikováno v: PLoS ONE, Vol 13, Iss 9, p e0201560 (2018)
INTRODUCTION:Proliferative glomerulonephritis manifests in a range of renal diseases and is characterized by the influx of inflammatory cells into the glomerulus. Heparan sulfate (HS) is an important (co-)receptor for binding of chemokines, cytokines
Externí odkaz: https://doaj.org/article/30450cdfa715488aab0838bc45c87e5b
Zobrazit plný text záznamu
2
Brody syndrome: A clinically heterogeneous entity distinct from Brody disease: A review of literature and a cross-sectional clinical study in 17 patients
Autor: N C, Voermans, A E, Laan, A, Oosterhof, T H, van Kuppevelt, G, Drost, M, Lammens, E J, Kamsteeg, C, Scotton, F, Gualandi, V, Guglielmi, L, van den Heuvel, G, Vattemi, B G, van Engelen
Publikováno v: Neuromuscular Disorders, 22, 11, pp. 944-54
Neuromuscular Disorders, 22, 944-54
Item does not contain fulltext Brody disease is a rare inherited myopathy due to reduced sarcoplasmic reticulum Ca(2+) ATPase (SERCA)1 activity caused by mutations in ATP2A1, which causes delayed muscle relaxation and silent cramps. So far the diseas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9fc1dc66935049460f424a8f8f7fe7aa
http://hdl.handle.net/11562/425137
Zobrazit plný text záznamu
3
Towards embryonic-like scaffolds for skin tissue engineering: identification of effector molecules and construction of scaffolds
Autor: P J E, Uijtdewilligen, E M M, Versteeg, C, Gilissen, S V, van Reijmersdal, R, Schoppmeyer, R G, Wismans, W F, Daamen, T H, van Kuppevelt
Publikováno v: Journal of tissue engineering and regenerative medicine. 10(1)
Autologous skin grafts are the gold standard for the treatment of burn wounds. In a number of cases, treatment with autologous tissue is not possible and skin substitutes are used. The outcome, however, is not optimal and improvements are needed. Ins
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f968f315aefb587dd1f35ef2d8815374
https://pubmed.ncbi.nlm.nih.gov/23468399
Zobrazit plný text záznamu
4
Elastic fiber abnormalities in hypermobility type Ehlers-Danlos syndrome patients with tenascin-X mutations
Autor: M C, Zweers, W B, Dean, T H, van Kuppevelt, J, Bristow, J, Schalkwijk
Publikováno v: Clinical genetics. 67(4)
Ehlers-Danlos syndrome (EDS) is a heterogeneous group of connective tissue disorders with characteristic skin and joint involvement. The concept that EDS is a disease of fibrillar collagen was challenged by the identification of a clinically distinct
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3fac9c54b821f73390e67d4b169146fc
https://pubmed.ncbi.nlm.nih.gov/15733269
Zobrazit plný text záznamu
6
Structural and functional studies on different human FABP types
Autor: J H, Veerkamp, H T, van Moerkerk, C F, Prinsen, T H, van Kuppevelt
Publikováno v: Molecular and cellular biochemistry. 192(1-2)
Interaction of various ligands with recombinant proteins of 5 human FABP types was studied by radiochemical and fluorescence procedures. Liver, heart, intestinal and myelin FABP showed a higher affinity for oleic acid than adipocyte FABP. Intestinal
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9cf17405aedd819f17d6af07c986e2aa
https://pubmed.ncbi.nlm.nih.gov/10331668
Zobrazit plný text záznamu
7
Generation and application of type-specific anti-heparan sulfate antibodies using phage display technology. Further evidence for heparan sulfate heterogeneity in the kidney
Autor: T H, van Kuppevelt, M A, Dennissen, W J, van Venrooij, R M, Hoet, J H, Veerkamp
Publikováno v: The Journal of biological chemistry. 273(21)
Detailed analysis of various heparan sulfate (HS) species is seriously hampered by a lack of appropriate tools, such as antibodies. We adopted phage display technology to generate anti-HS antibodies. A "single pot" semisynthetic human antibody phage
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ad3a1da29d24695908a962921108d54e
https://pubmed.ncbi.nlm.nih.gov/9582329
Zobrazit plný text záznamu
9
Ultrastructural localization and characterization of proteoglycans in human lung alveoli
Autor: T H, van Kuppevelt, F P, Cremers, J G, Domen, H M, van Beuningen, A J, van den Brule, C M, Kuyper
Publikováno v: European journal of cell biology. 36(1)
In order to localize and characterize proteoglycans in human lung alveoli, we have used the cationic dye Cuprolinic Blue according to the critical electrolyte concentration method. After staining, five types of Cuprolinic Blue-positive filaments beco
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0f44fc195d4d2116dac529719310a9b2
https://pubmed.ncbi.nlm.nih.gov/3979403
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje