Zobrazeno 1 - 10
of 466
pro vyhledávání: '"R. Bye"'
Publikováno v:
طب جانباز, Vol 2, Iss 3, Pp 50-57 (2010)
Background and purpose: Limb loss is a phenomenon that induces disability in patient undergoing amputation. Amputation is needed in treatment of war related patients and most of amputees suffer of chronic amputation-related pain. Information about ou
Externí odkaz:
https://doaj.org/article/92071dc4735242aab4166c7612f59b8a
Autor:
Christopher R. Bye, Vanessa Penna, Isabelle R. de Luzy, Carlos W. Gantner, Cameron P.J. Hunt, Lachlan H. Thompson, Clare L. Parish
Publikováno v:
Stem Cell Reports, Vol 13, Iss 5, Pp 877-890 (2019)
Summary: Human pluripotent stem cells are a valuable resource for transplantation, yet our ability to profile xenografts is largely limited to low-throughput immunohistochemical analysis by difficulties in readily isolating grafts for transcriptomic
Externí odkaz:
https://doaj.org/article/0e598a0cee5549228249d77dc5f7ee16
Autor:
Restuadi Restuadi, Frederik J. Steyn, Edor Kabashi, Shyuan T. Ngo, Fei-Fei Cheng, Marta F. Nabais, Mike J. Thompson, Ting Qi, Yang Wu, Anjali K. Henders, Leanne Wallace, Chris R. Bye, Bradley J. Turner, Laura Ziser, Susan Mathers, Pamela A. McCombe, Merrilee Needham, David Schultz, Matthew C. Kiernan, Wouter van Rheenen, Leonard H. van den Berg, Jan H. Veldink, Roel Ophoff, Alexander Gusev, Noah Zaitlen, Allan F. McRae, Robert D. Henderson, Naomi R. Wray, Jean Giacomotto, Fleur C. Garton
Publikováno v:
Genome Medicine
Genome Medicine, 2022, 14 (1), pp.7. ⟨10.1186/s13073-021-01006-6⟩
Genome medicine, vol 14, iss 1
Genome Medicine, Vol 14, Iss 1, Pp 1-22 (2022)
Genome Medicine, 2022, 14 (1), pp.7. ⟨10.1186/s13073-021-01006-6⟩
Genome medicine, vol 14, iss 1
Genome Medicine, Vol 14, Iss 1, Pp 1-22 (2022)
Background Amyotrophic lateral sclerosis (ALS) is a complex, late-onset, neurodegenerative disease with a genetic contribution to disease liability. Genome-wide association studies (GWAS) have identified ten risk loci to date, including the TNIP1/GPX
Akademický článek
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Publikováno v:
The Journal of Neuroscience. 39:6656-6667
The growth of axons corresponding to different neuronal subtypes is governed by unique expression profiles of molecules on the growth cone. These molecules respond to extracellular cues either locally though cell adhesion interactions or over long di
Autor:
Pardis F. Zanganeh, Samantha K. Barton, Katherine Lim, Elizabeth L. Qian, Duncan E. Crombie, Christopher R. Bye, Bradley J. Turner
Publikováno v:
Brain communications. 4(2)
Amyotrophic lateral sclerosis is a late-onset adult neurodegenerative disease, although there is mounting electrophysiological and pathological evidence from patients and animal models for a protracted preclinical period of motor neuron susceptibilit
Publikováno v:
Revista Cubana de Medicina General Integral, Vol 14, Iss 4, Pp 374-389 (1998)
El embarazo entre las adolescentes ha aumentado en la última década1-5 asociado con frecuencia a la pobreza, al bajo nivel cultural y a una inadecuada atención prenatal. Aunque se ha sugerido que los resultados adversos del embarazo son más comun
Externí odkaz:
https://doaj.org/article/9f25ab9fe19646d2a7425ccc50978158
Autor:
Michael J. Thompson, Noah Zaitlen, Edor Kabashi, Naomi R. Wray, Fei-Fei Cheng, Matthew C. Kiernan, Leanne Wallace, Shyuan T. Ngo, David Schultz, Robert D. Henderson, Susan Mathers, Merrilee Needham, Jean Giacomotto, Allan F. McRae, Christopher R. Bye, Leonard H. van den Berg, Bradley J. Turner, Anjali K. Henders, Restuadi Restuadi, Marta F. Nabais, Wouter van Rheenen, Frederik J. Steyn, Laura Ziser, Jan H. Veldink, Alexander Gusev, Ting Qi, Roel A. Ophoff, Pamela A. McCombe, Fleur C. Garton
Publikováno v:
SSRN Electronic Journal.
Amyotrophic lateral sclerosis (ALS) is a complex late-onset, neurodegenerative disease with a genetic contribution to disease liability. Genome-wide association studies have identified eleven risk loci to date, including the TNIP1/GPX3 locus on chrom
Autor:
Jessica A. Kauhausen, Niamh Moriarty, Colin W. Pouton, Carlos W. Gantner, Jonathan C. Niclis, Lachlan H. Thompson, Vanessa Penna, Christopher R. Bye, Deniz Kirik, Clare L. Parish, Isabelle R. de Luzy, Cameron P.J. Hunt, Charlotte M. Ermine
The derivation of neurotransmitter and region-specific neuronal populations from human pluripotent stem cells (PSC) provides impetus for advancing cell therapies into the clinic. At the forefront is our ability to generate ventral midbrain (VM) dopam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa2d52c38b2bf6602a7ce44a8a0a21b2
Autor:
Brette D Blakely, Christopher R Bye, Chathurini V Fernando, Malcolm K Horne, Maria L Macheda, Steven A Stacker, Ernest Arenas, Clare L Parish
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e18373 (2011)
During development, precise temporal and spatial gradients are responsible for guiding axons to their appropriate targets. Within the developing ventral midbrain (VM) the cues that guide dopaminergic (DA) axons to their forebrain targets remain to be
Externí odkaz:
https://doaj.org/article/ea38d9ffb4af4b8f8612bfd5fd0c9afe