Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Bradley J, Hurren"'
Autor:
Natasha AMS Flack, Katie Frost, Shanmugapriya Aravazhi, Athena Macmillan, Phil Blyth, Stephanie J. Woodley, Helen D. Nicholson, Bradley J. Hurren, Rebecca J. Bird
Publikováno v:
Education Sciences, Vol 12, Iss 7, p 451 (2022)
Human-cadaveric material is a valuable resource for teaching anatomy, and a lot of research engaging medical students shows they benefit, in a variety of ways, from engaging with this material. However, more and more students who study anatomy are no
Externí odkaz:
https://doaj.org/article/acc57e59f3804528bffb1ebb828a6b0a
Autor:
Bird, Natasha AMS Flack, Katie Frost, Shanmugapriya Aravazhi, Athena Macmillan, Phil Blyth, Stephanie J. Woodley, Helen D. Nicholson, Bradley J. Hurren, Rebecca J.
Publikováno v:
Education Sciences; Volume 12; Issue 7; Pages: 451
Human-cadaveric material is a valuable resource for teaching anatomy, and a lot of research engaging medical students shows they benefit, in a variety of ways, from engaging with this material. However, more and more students who study anatomy are no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::c033f73bf2e5ff53b7af9ff699f4c7ec
Autor:
Rebecca J. Bird, Bradley J. Hurren
Publikováno v:
Clinical Anatomy. 29:606-619
Klinefelter's syndrome, the most common sex disorder associated with chromosomal aberrations, is characterized by a plethora of clinical features. Parameters for diagnosis of the syndrome are constantly expanding as new anatomical and hormonal abnorm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8174991c1286a91f1c15451251f9e425
https://doi.org/10.1002/ca.22695
https://doi.org/10.1002/ca.22695
Publikováno v:
Clinical Anatomy. 29:590-605
Prader-Willi Syndrome (PWS) is estimated to affect 400,000 people worldwide. First described clinically in 1956, PWS is now known to be a result of a genetic mutation, involving Chromosome 15. The phenotypical appearance of individuals with the syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11b79fcdd89385aa7f0eccfd724204fe
https://doi.org/10.1002/ca.22686
https://doi.org/10.1002/ca.22686
Publikováno v:
Clinical anatomy (New York, N.Y.). 29(5)
Prader-Willi Syndrome (PWS) is estimated to affect 400,000 people worldwide. First described clinically in 1956, PWS is now known to be a result of a genetic mutation, involving Chromosome 15. The phenotypical appearance of individuals with the syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c244269361a46b3ac15a759ff9aac9a
https://pubmed.ncbi.nlm.nih.gov/26749552
https://pubmed.ncbi.nlm.nih.gov/26749552
Autor:
Adele G. Woolley, Marilyn J. Duxson, Philip W. Sheard, Karen J. Tait, Bradley J. Hurren, Lorryn Fisher
Publikováno v:
Glia. 56(3)
This work investigates the role of NT-3 in peripheral myelination. Recent articles, based in vitro, propose that NT-3 acting through its high-affinity receptor TrkC may act to inhibit myelin formation by enhancing Schwann cell motility and/or migrati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34ccbf191251326407f43167684ab688
https://pubmed.ncbi.nlm.nih.gov/18080292
https://pubmed.ncbi.nlm.nih.gov/18080292
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 7, p e0133811 (2015)
PLoS ONE, Vol 10, Iss 7, p e0133811 (2015)
Skeletal muscle development has been the focus of intensive study for many decades. Recent advances in genetic manipulation of the mouse have increased our understanding of the cell signalling involved in the development of muscle progenitors which g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd411f6e62caa1dc800a9fa60436616f
https://doi.org/10.1371/journal.pone.0133811
https://doi.org/10.1371/journal.pone.0133811