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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Gene Review

gs  -  glabrous

Mus musculus

 
 
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High impact information on gs

 

Biological context of gs

 

Anatomical context of gs

  • Using morphological studies we now show that Merkel cells develop normally in both hairy and glabrous skin in these animals until 2 weeks old, but are progressively lost thereafter and have almost completely disappeared 2 months after birth [9].
  • Using an in vivo mouse preparation, we studied response properties of tibial nerve afferent fibers innervating glabrous skin [10].
  • Response properties of mechanoreceptors and nociceptors in mouse glabrous skin: an in vivo study [10].
  • The majority of PACAP-positive nerve fibres are, however, located in the glabrous skin of the nipple and the hairy skin adjacent to the nipple forming a subepithelial plexus from which delicate varicose nerve fibres enter the overlying epithelium [11].
  • The distribution of ATPase-positive Langerhans' cells was investigated in whole sheets of the glabrous sole-of-foot epidermis of the mouse [12].
 

Other interactions of gs

  • These results suggest that BDNF is the only TrkB ligand involved in the development of Meissner corpuscles in murine glabrous skin, and it probably regulates the development of the sensory neurons that innervate Meissner corpuscles [13].
 

Analytical, diagnostic and therapeutic context of gs

References

  1. Location of stem cells of human hair follicles by clonal analysis. Rochat, A., Kobayashi, K., Barrandon, Y. Cell (1994) [Pubmed]
  2. CD24 (heat stable antigen, nectadrin), a novel keratinocyte differentiation marker, is preferentially expressed in areas of the hair follicle containing the colony-forming cells. Magnaldo, T., Barrandon, Y. J. Cell. Sci. (1996) [Pubmed]
  3. Neural crest origin of mammalian Merkel cells. Szeder, V., Grim, M., Halata, Z., Sieber-Blum, M. Dev. Biol. (2003) [Pubmed]
  4. Sex differences in the densities of epidermal Langerhans cells of the mouse. Koyama, Y., Nagao, S., Ohashi, K., Takahashi, H., Marunouchi, T. J. Invest. Dermatol. (1987) [Pubmed]
  5. Overexpression of neurotrophin 4 in skin enhances myelinated sensory endings but does not influence sensory neuron number. Krimm, R.F., Davis, B.M., Noel, T., Albers, K.M. J. Comp. Neurol. (2006) [Pubmed]
  6. Effects of neutralizing antibodies to TNF-alpha on pain-related behavior and nerve regeneration in mice with chronic constriction injury. Lindenlaub, T., Teuteberg, P., Hartung, T., Sommer, C. Brain Res. (2000) [Pubmed]
  7. Surface characteristics of oocytes from juvenile mice as observed in the scanning electron microscope. von Weymarn, N., Guggenheim, R., Müller, H. Anat. Embryol. (1980) [Pubmed]
  8. Virulence profile of ten Paracoccidioides brasiliensis isolates: association with morphologic and genetic patterns. Kurokawa, C.S., Lopes, C.R., Sugizaki, M.F., Kuramae, E.E., Franco, M.F., Peraçoli, M.T. Rev. Inst. Med. Trop. Sao Paulo (2005) [Pubmed]
  9. Postnatal loss of Merkel cells, but not of slowly adapting mechanoreceptors in mice lacking the neurotrophin receptor p75. Kinkelin, I., Stucky, C.L., Koltzenburg, M. Eur. J. Neurosci. (1999) [Pubmed]
  10. Response properties of mechanoreceptors and nociceptors in mouse glabrous skin: an in vivo study. Cain, D.M., Khasabov, S.G., Simone, D.A. J. Neurophysiol. (2001) [Pubmed]
  11. Pituitary adenylate cyclase activating polypeptide (PACAP) in the rat mammary gland. Skakkebaek, M., Hannibal, J., Fahrenkrug, J. Cell Tissue Res. (1999) [Pubmed]
  12. Langerhans' cell-free regions in orthokeratinizing sole-of-foot epidermis of the adult mouse. Schweizer, J. Arch. Dermatol. Res. (1980) [Pubmed]
  13. BDNF, but not NT-4, is necessary for normal development of Meissner corpuscles. González-Martínez, T., Fariñas, I., Del Valle, M.E., Feito, J., Germanà, G., Cobo, J., Vega, J.A. Neurosci. Lett. (2005) [Pubmed]
 
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