Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Paul Holden"'
Autor:
Paul Holden, Alma Pekmezovic
Publikováno v:
Asia & the Pacific Policy Studies, Vol 7, Iss 3, Pp 247-261 (2020)
Abstract While there have been several attempts to measure the investment climate, by far the most widely recognised measure is the World Bank's Doing Business indicators (DBIs), ranking some 200 countries on their ease of doing business. Methodologi
Externí odkaz:
https://doaj.org/article/da35ac8eba7a4a88ae6f2ed28ad5fb42
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-12 (2017)
Abstract Background Collagen VI is a ubiquitously-expressed macromolecule that forms unique microfibrillar assemblies in the extracellular matrix. Mutations in the COL6A1, COL6A2 and COL6A3 genes result in congenital muscular dystrophy, arguing that
Externí odkaz:
https://doaj.org/article/a458c516f1024473b26c1af5278fafd6
Autor:
Donna Luff, Sara W. Buscher, Valerie L. Ward, Sonia A. Ballal, Paul Holden, Rachelle Pierre, Paul Won, Eun Jin Yu, Sara L. Toomey
Publikováno v:
Pediatrics. 150
BACKGROUND AND OBJECTIVE Racial and ethnic and socioeconomic differences in patient experience are prevalent and can negatively impact health outcomes. Our objective was to examine differences in family experience of care in the pediatric ambulatory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::192f5a4cb548cf440fa9fb32a33b23f5
https://doi.org/10.1542/peds.2021-056001
https://doi.org/10.1542/peds.2021-056001
Autor:
Paul Holden, Cecilia Giunta, Pei Jin Lim, Yoshihiro Ishikawa, Nobuyo Mizuno, Marianne Rohrbach, Hans Peter Bächinger, Douglas B. Gould
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific reports, vol 10, iss 1
Scientific Reports
Scientific reports, vol 10, iss 1
Scientific Reports
Mutations in the FKBP14 gene encoding FKBP22 (FK506 Binding Protein 22 kDa) cause kyphoscoliotic Ehlers-Danlos Syndrome (kEDS). The first clinical report showed that a lack of FKBP22 protein due to mutations causing nonsense-mediated decay of the mRN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41b08c8b2fc4c8d372f1ee406b7438d1
http://link.springer.com/article/10.1038/s41598-019-57374-y
http://link.springer.com/article/10.1038/s41598-019-57374-y
Publikováno v:
Standing between Life and Extinction ISBN: 9780226694474
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d65618dc066004f7942143fdeecd06bf
https://doi.org/10.7208/chicago/9780226694504.003.0011
https://doi.org/10.7208/chicago/9780226694504.003.0011
Autor:
Yoshihiro Ishikawa, Antti M. Salo, Hans Peter Bächinger, Douglas R. Keene, Sara F. Tufa, Kazunori Mizuno, Nobuyo Mizuno, Keith D. Zientek, Paul Holden, Olesya Semenova, Johanna Myllyharju, Yuki Taga
Collagen is the most abundant protein in humans and is heavily post-translationally modified. Its biosynthesis is very complex and requires three different types of hydroxylation (two for proline and one for lysine) that are generated in the rough en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c73d8418eb88f1d1c1272809fdcf1b8
Autor:
Paul Holden
Publikováno v:
The Antiquaries Journal. 99:469-471
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e36d4516f6b87ee3a37c026198a19b88
https://doi.org/10.1017/s0003581519000337
https://doi.org/10.1017/s0003581519000337
Autor:
Sara F. Tufa, Johanna Myllyharju, Douglas R. Keene, Kazunori Mizuno, Paul Holden, Hans Peter Bächinger, Douglas B. Gould, Olesya Semenova, Yuki Taga, Nobuyo Mizuno, Keith D. Zientek, Yoshihiro Ishikawa, Antti M. Salo
Publikováno v:
The Journal of Biological Chemistry
Collagen is the most abundant protein in humans. It has a characteristic triple-helix structure and is heavily posttranslationally modified. The complex biosynthesis of collagen involves processing by many enzymes and chaperones in the rough endoplas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::963794e96db27b45cf8823e1b8528806
https://doi.org/10.1016/j.jbc.2021.100453
https://doi.org/10.1016/j.jbc.2021.100453
Publikováno v:
Clinical Dysmorphology. 25:152-155
This study aimed to identify the genetic basis of a severe skeletal lethal dysplasia. The main clinical features of two affected fetuses included short limbs with flared metaphyses, bowed radii, femora and tibiae, irregular ossification of hands and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d220a2be71d228a884bce1d65a75303
https://doi.org/10.1097/mcd.0000000000000136
https://doi.org/10.1097/mcd.0000000000000136
Autor:
Paul Holden
Publikováno v:
Architectural History. 60:349-351
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbf5885024e5491710b581ee7812eff2
https://doi.org/10.1017/arh.2017.15
https://doi.org/10.1017/arh.2017.15