Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Medard Hadonou"'
Autor:
Pratik Shah, Antonia Clarke, I C Lloyd, John Short, Sharon Ocansey, Patricia Atkinson, Albanese Assunta, Meriel McEntagart, Medard Hadonou, Charlene Crosby, Debbie Pullen, Damian Smedley
Publikováno v:
Clinical Dysmorphology. 31:11-17
DNAJC3, a co-chaperone of BiP, is a member of the heat shock protein family. These proteins are produced in the endoplasmic reticulum (ER) to counter cell stress resulting from healthy functional protein processing. Dysregulation of unfolded proteins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7c193dc67ef51bc823353b05e45a8ba
https://doi.org/10.1097/mcd.0000000000000397
https://doi.org/10.1097/mcd.0000000000000397
Autor:
Damien Smedley, Hailey Pinz, Chiara Kloechner, Grazia M.S. Mancini, Anna de Burca, Christopher T. Gordon, Emilia K. Bijlsma, Rebecca Wilaert, Jonas Denecke, Ingo Helbig, Nicola Brunetti-Pierri, Martina Wilke, Katta M. Girisha, Parmeet Kaur, Jeanne Amiel, Janette diMonda, Rolph Pfundt, Maya Chopra, Maria Arelin, Julie Evans, Hermine E. Veenstra-Knol, Micheil Innes, Kyra E. Stuurman, Janvier Porta Pelayo, Ugur Hodoglugil, Meriel McEntagart, Rosan Lechner, Anupriya Kaur, Sam Amin, Sarah E McKeown, Maja Hempel, Tjitske Kleefstra, Michelle L. Thompson, Tiffany Yip, Maggie Williams, Amelia Kirby, Jane Juusola, Anna Lehman, Gerarda Capuccio, Frank Sleutels, Rami Abou Jamra, Konrad Platzer, William A. Weiss, Martina Bebin, Jennifer Semotok, Stanislas Lyonnet, Naomi Yachelevich, Anni Niskakoski, Juanita Neira, Anne Slavotinek, Cacha Peters-Scholte, Usha Kini, Medard Hadonou, Mariëtte J.V. Hoffer, Anju Shukla, Sajel Lala, John Short, Susanne B. Kamphausen, Katherine L. Helbig, Sarah F. Smithson, Fanny Kortüm, Sandra Yang, Jill Clayton-Smith, Amy Whittle, Alberto Fernández-Jaen
Publikováno v:
Molecular Genetics and Metabolism. 132:S99
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb68c45eeb0a5d839c708a94525f2105
https://doi.org/10.1016/s1096-7192(21)00233-x
https://doi.org/10.1016/s1096-7192(21)00233-x
Autor:
Graham D. Moores, Alan L. Devonshire, Medard Hadonou, Juha Uitto, Martin S. Williamson, Kari Kataja, Christian Oker-Blom
Publikováno v:
Structure and Function of Cholinesterases and Related Proteins ISBN: 9781489915429
The baculovirus expression system was employed for production of a modified, FLAG-epitope tagged Musca domestica acetylcholinestearse (AChE) in Sf9 cells. The signal peptide of ecdysteroid UDP-glycosyltransferase (EGT) of Autographa californica nucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7c95bdb22b488b78b200bc241debc54
https://doi.org/10.1007/978-1-4899-1540-5_145
https://doi.org/10.1007/978-1-4899-1540-5_145
Autor:
Colette Duez, Josette Lamotte-Brasseur, Daniel Klein, Jean-Marie Ghuysen, Jean-Marc Wilkin, Bernard Joris, Louis Varetto, Ayaovi Medard Hadonou, Jean-Marie Frère
Publikováno v:
European journal of biochemistry. 207(1)
The importance of various residues in the Streptomyces R61 penicillin-sensitive DD-peptidase has been assessed by site-directed mutagenesis. The replacement of the active Ser62 by a Cys residue yielded an inactive protein which was also unable to rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a294b95cbe6666cd77edf30c394b4a72
https://pubmed.ncbi.nlm.nih.gov/1628665
https://pubmed.ncbi.nlm.nih.gov/1628665
Autor:
M Adam, Ayaovi Medard Hadonou, Bernard Joris, Jean-Marie Frère, Marc Jamin, Jean-Marie Ghuysen, Jean Dusart
Among the active-site-serine penicillin-recognizing proteins, the Streptomyces R61 extracellular DD-peptidase is the only one to have a His-Thr-Gly sequence [instead of Lys-Thr(Ser)-Gly] in ‘box’ VII. The His residue was replaced by Gln or Lys. B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::833efc69a1aae0405a0f521be7ece295
https://europepmc.org/articles/PMC1130807/
https://europepmc.org/articles/PMC1130807/
Publikováno v:
Blood. 108:1026-1026
Von Willebrand disease (VWD) is an autosomal bleeding disorder caused by qualitative (type 2 VWD) or quantitative (type 1 and type 3 VWD) defects of plasma VWF: complete absence of VWF from plasma distinguishes type 3 from the partial deficiency type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d1e0be93fa0936ba7cd60bf7fc81677
https://doi.org/10.1182/blood.v108.11.1026.1026
https://doi.org/10.1182/blood.v108.11.1026.1026
Autor:
Jaqueline A. Cutler, Michael Mitchell, Geoffrey F. Savidge, Medard Hadonou, Bella Madan, Purvee Harrington
Publikováno v:
Blood. 106:1784-1784
Von Willebrand disease (vWD) (MIM 193400) is a heterogeneous bleeding disorder caused by both quantitative (type 1 and 3) and qualitative (type 2) defects of von Willebrand factor. Whilst type 2 vWD has been reasonably well studied, due to the locali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cab3f197212c09e470e8b62e149fb315
https://doi.org/10.1182/blood.v106.11.1784.1784
https://doi.org/10.1182/blood.v106.11.1784.1784