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• Germline mutation of INI1/SMARCB1 in familial schwannomatosis.

  Patients with schwannomatosis develop multiple schwannomas but no vestibular schwannomas diagnostic of neurofibromatosis type 2. We report an inactiva…

  Authors: Theo J M Hulsebos, Astrid S Plomp, Ruud A Wolterman, Els C Robanus-Maandag, Frank Baas, Pieter Wesseling

  Source: American journal of human genetics. 2007 Apr

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• Myelination competent conditionally immortalized mouse Schwann cells.

  Numerous mouse myelin mutants are available to analyze the biology of the peripheral nervous system related to health and disease in vivo. However, ro…

  Authors: José T Saavedra, Ruud A Wolterman, Frank Baas, Anneloor L M A ten Asbroek

  Source: Journal of neuroscience methods. 2008 Sep 15

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