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Yanling Wang

Researcher at Stockholm University

Publications -  5
Citations -  75

Yanling Wang is an academic researcher from Stockholm University. The author has contributed to research in topics: Cell growth & Brown adipose tissue. The author has an hindex of 4, co-authored 5 publications receiving 63 citations.

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Journal ArticleDOI

Cell proliferation and apoptosis inhibition: essential processes for recruitment of the full thermogenic capacity of brown adipose tissue.

TL;DR: This unique ability of norepinephrine to increase cell number in an apparently mitogenically dormant tissue provides possibilities to augment the metabolic capacity of brown adipose tissue, also for therapeutic purposes.
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Non-transactivational, dual pathways for LPA-induced Erk1/2 activation in primary cultures of brown pre-adipocytes.

TL;DR: It is found that LPA could induce Erk1/2 activation, and this implies that in non-transformed systems, RTK transactivation may not be involved in the mediation of GPCR-induced Erk 1/2 MAP kinase activation.
Journal ArticleDOI

Protein kinase a-mediated cell proliferation in brown preadipocytes is independent of Erk1/2, PI3K and mTOR.

TL;DR: It is demonstrated that, in contrast to other systems where the mitogenic effect of cAMP requires the synergistic action of (serum) growth factors, especially insulin/IGF, the cAMP effect in brown preadipocytes was independent of serum and insulin.
Journal ArticleDOI

In brown adipocytes, adrenergically induced β1-/β3-(Gs)-, α2-(Gi)- and α1-(Gq)-signalling to Erk1/2 activation is not mediated via EGF receptor transactivation

TL;DR: In this article, the EGF receptor kinase inhibitor AG1478 had no significant effect on EGF-induced Erk1/2 activation induced by any of these adrenergic agonists.

Identifying novel genes involved in cAMP- induced cell proliferation of brown preadi- pocytes

TL;DR: Norepinephrine, through the second messenger cAMP, stimulates cell prolif- eration in a variety of cell types including brown preadipocytes, however, the cell signalling pathway mediating the cAMP pathway is unclear.