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J Exp Biol (2019) 222 (20): jeb213348.
Published: 24 October 2019
... remodeling, which may enhance foraging ability, predator avoidance and dispersal overland. Skeletal muscle Red oxidative muscle Lactate Angiogenesis Tail-flip jumping Mitochondrial content Locomotor movement on land is far more costly than movement in water ( Schmidt-Nielsen, 1972...
J Exp Biol (2019) 222 (2): jeb186486.
Published: 17 January 2019
... ( P crit ), higher regulation index (RI)] after only 1 day of air exposure, and these changes were strongly associated with the change in hematocrit and dorsal cutaneous angiogenesis. Additionally, we found that 1 h of air exposure induced the expression of four angiogenesis-associated genes – vegfa...
Includes: Supplementary data
Guang Wang, Nuan Zhang, Yi-Fan Wei, Yi-Mei Jin, Shi-Yao Zhang, Xin Cheng, Zheng-Lai Ma, Shu-Zhu Zhao, You-Peng Chen, Manli Chuai, Berthold Hocher, Xuesong Yang
J Exp Biol (2015) 218 (21): 3468–3477.
Published: 1 November 2015
... mortality at early stages mainly results from defects in cardiovascular development, we focused on heart formation and angiogenesis. We found that high-salt exposure enhanced the risk of abnormal heart tube looping and blood congestion in the heart chamber. In the presence of high salt, both ventricular...
J Exp Biol (2010) 213 (19): 3340–3347.
Published: 1 October 2010
... the VDE and the chorioallantois in E. quoyii , allowing the simultaneous growth of both tissues. * Author for correspondence ( email@example.com ) 30 6 2010 © 2010. 2010 lizard viviparity uterus angiogenesis embryo Eulamprus quoyii Viviparity...
J Exp Biol (2010) 213 (16): 2865–2872.
Published: 15 August 2010
... relationship between loss of Hb and induction of angiogenesis that probably is mediated through nitric oxide signaling. The aggregate concentration of plasma NO x was measured in control and anemic (PHZ-treated) N. coriiceps as a proxy for NO ( Fig. 3 ). The plasma concentration of NO x in N. coriiceps...
J Exp Biol (2009) 212 (11): 1707–1715.
Published: 1 June 2009
... secretion), water movement into and out of the brain, cell migration(angiogenesis, tumor metastasis, wound healing) and neural function (sensory signaling, seizures). A subset of aquaporins that transport both water and glycerol, the `aquaglyceroporins', regulate glycerol content in epidermal, fat and other...
J Exp Biol (2004) 207 (18): 3163–3169.
Published: 15 August 2004
... begins after about 1 week of hypoxic exposure and is completed by 3 weeks. Hypoxic angiogenesis is controlled by activation of downstream genes by Hypoxia Inducible Factor-1 and Angiopoietin-2. The processes that increase capillary density are reversible upon restoration of the ambient oxygen...
J Exp Biol (2004) 207 (18): 3233–3242.
Published: 15 August 2004
... ischaemia neuroprotection angiogenesis VEGF preconditioning tolerance Many of the hypoxic adaptation processes in the body are based on transcriptional regulation by the hypoxia-inducible factors HIF-1 and HIF-2. HIF targets include genes involved in angiogenesis, vasomotor control, energy...
J Exp Biol (2003) 206 (8): 1299–1307.
Published: 15 April 2003
...Thorsten Schwerte; Dietmar Überbacher; Bernd Pelster SUMMARY This is the first study to use a combination of digital imaging techniques and vital video microscopy to study hypoxia-induced changes in blood cell concentration, angiogenesis and blood redistribution in entire animals. Zebrafish Danio...
J Exp Biol (2002) 205 (6): 829–840.
Published: 15 March 2002
... fibre types in skeletal muscle on cold-acclimation, and only modest differences were seen in activity of oxidative or glycolytic enzymes in either species. However, adjustments in Type II fibre size paralleled the muscle hypertrophy in rat and atrophy in hamster. Cold-induced angiogenesis was present...