Search Results - "van de Wetering, C."

  • Showing 1 - 7 results of 7
Refine Results
  1. 1

    Lymphoma development in Bax transgenic mice is inhibited by Bcl-2 and associated with chromosomal instability by Luke, J J, Van De Wetering, C I, Knudson, C M

    Published in Cell death and differentiation (01-06-2003)
    “…Bax is a Bcl-2 family member that promotes apoptosis but has paradoxical effects on lymphoma development in p53-deficient mice. To better understand the…”
    Get full text
    Journal Article
  2. 2

    Seagrass spatial data synthesis from north‐east Australia, Torres Strait and Gulf of Carpentaria, 1983 to 2022 by Carter, A, McKenna, S, Rasheed, MA, Taylor, H, Wetering, C, Chartrand, K, Reason, C, Collier, C, Shepherd, L, Mellors, J, McKenzie, L, Duke, NC, Roelofs, A, Smit, N, Groom, R, Barrett, D, Evans, S, Pitcher, R, Murphy, N, Carlisle, M, David, M, Lui, S, Coles, RG

    Published in Limnology and oceanography letters (01-02-2024)
    “…The Gulf of Carpentaria and Torres Strait in north‐eastern Australia support globally significant seagrass ecosystems that underpin fishing and cultural…”
    Get full text
    Journal Article
  3. 3
  4. 4
  5. 5

    Widespread Dispersal of Cholera Toxin Subunit b to Brain and Spinal Cord Neurons Following Systemic Delivery by Alisky, Joseph M., van de Wetering, Christopher I., Davidson, Beverly L.

    Published in Experimental neurology (01-11-2002)
    “…We have discovered novel transport properties of cholera toxin subunit b beyond well-known anterograde and retrograde axonal transport. Injection of 1500 μg of…”
    Get full text
    Journal Article
  6. 6

    Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35 --> q36.1 and identification of an intragenic genetic marker by van den Maagdenberg, A M, Olde Weghuis, D, Rijss, J, van de Wetering, R A, Wieringa, B, Geurts van Kessel, A, Hendriks, W J

    Published in Cytogenetics and cell genetics (01-01-1996)
    “…Using a mouse protein tyrosine phosphatase cDNA fragment as a probe, cosmid clones containing segments of the human IA-2 PTPase gene (PTPRN) were isolated. The…”
    Get more information
    Journal Article
  7. 7

    Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene by van de Wetering, R.A.C, Gabreëls-Festen, A.A.W.M, Timmerman, V, Padberg, G.W, Gabreëls, F.J.M, Mariman, E.C.M

    Published in Neuromuscular disorders : NMD (01-10-2002)
    “…Hereditary neuropathy with liability to pressure palsies is associated with a deficiency in the Peripheral Myelin Protein 22 (PMP22). Most hereditary…”
    Get full text
    Journal Article