Impaired Hypothalamic Regulation of Endocrine Function and Delayed Counterregulatory Response to Hypoglycemia in Magel2-Null Mice von Tennese, Alysa A, Wevrick, Rachel

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Essential role for the Prader–Willi syndrome protein necdin in axonal outgrowth von Lee, Syann, Walker, Christine L., Karten, Barbara, Kuny, Sharee L., Tennese, Alysa A., O'Neill, Megan A., Wevrick, Rachel

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Four Lymphomas in 1 Patient: A Unique Case of Triple Composite Non-Hodgkin Lymphoma Followed by Classical Hodgkin Lymphoma von Tennese, Alysa, Skrabek, Pamela J., Nasr, Michel R., Sekiguchi, Debora R., Morales, Carmen, Brown, Theresa C., Weisenburger, Dennis D., Perry, Anamarija M.

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Loss of the Prader‐Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons von Tennese, Alysa A., Gee, Christopher B., Wevrick, Rachel

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The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations von Frosk, Patrick, Greenberg, Cheryl R., Tennese, Alysa A.P., Lamont, Ryan, Nylen, Edward, Hirst, Cheryl, Frappier, Danielle, Roslin, Nicole M., Zaik, Michaela, Bushby, Kate, Straub, Volker, Zatz, Mayana, de Paula, Flavia, Morgan, Kenneth, Fujiwara, T. Mary, Wrogemann, Klaus

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The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations von Frosk, Patrick, Greenberg, Cheryl R., Tennese, Alysa A.P., Lamont, Ryan, Nylen, Edward, Hirst, Cheryl, Frappier, Danielle, Roslin, Nicole M., Zaik, Michaela, Bushby, Kate, Straub, Volker, Zatz, Mayana, de Paula, Flavia, Morgan, Kenneth, Fujiwara, T. Mary, Wrogemann, Klaus

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