SEARCH

SEARCH BY CITATION

REFERENCES

  • Aizawa T, Maruyama K, Kondo H, Yoshikawa K. 1992. Expression of necdin, an embryonal carcinoma-derived nuclear protein, in developing mouse brain. Brain Res Dev Brain Res 68: 265274.
  • Andrieu D, Watrin F, Niinobe M, Yoshikawa K, Muscatelli F, Fernandez PA. 2003. Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression. Gene Expr Patterns 3: 761765.
  • Andrieu D, Meziane H, Marly F, Angelats C, Fernandez PA, Muscatelli F. 2006. Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death. BMC Dev Biol 6: 5661.
  • Badano JL, Teslovich TM, Katsanis N. 2005. The centrosome in human genetic disease. Nat Rev Genet 6: 194205.
  • Barker PA, Salehi A. 2002. The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease. J Neurosci Res 67: 705712.
  • Blasius TL, Cai D, Jih GT, Toret CP, Verhey KJ. 2007. Two binding partners cooperate to activate the molecular motor Kinesin-1. J Cell Biol 176: 1117.
  • Bloom L, Horvitz HR. 1997. The Caenorhabditis elegans gene unc-76 and its human homologs define a new gene family involved in axonal outgrowth and fasciculation. Proc Natl Acad Sci U S A 94: 34143419.
  • Boccaccio I, Glatt-Deeley H, Watrin F, Roeckel N, Lalande M, Muscatelli F. 1999. The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Hum Mol Genet 8: 24972505.
  • Choe YH, Jin DK, Kim SE, Song SY, Paik KH, Park HY, Oh YJ, Kim AH, Kim JS, Kim CW, Chu SH, Kwon EK, Lee KH. 2005. Hyperghrelinemia does not accelerate gastric emptying in Prader-Willi syndrome patients. J Clin Endocrinol Metab 90: 33673370.
  • de Anda FC, Pollarolo G, Da Silva JS, Camoletto PG, Feiguin F, Dotti CG. 2005. Centrosome localization determines neuronal polarity. Nature 436: 704708.
  • DiMario FJ Jr, Bauer L, Volpe J, Cassidy SB. 1996. Respiratory sinus arrhythmia in patients with Prader-Willi syndrome. J Child Neurol 11: 121125.
  • DiMario FJ Jr, Dunham B, Burleson JA, Moskovitz J, Cassidy SB. 1994. An evaluation of autonomic nervous system function in patients with Prader-Willi syndrome. Pediatrics 93: 7681.
  • Enomoto H, Crawford PA, Gorodinsky A, Heuckeroth RO, Johnson EM Jr, Milbrandt J. 2001. RET signaling is essential for migration, axonal growth and axon guidance of developing sympathetic neurons. Development 128: 39633974.
  • Ernfors P, Lee KF, Jaenisch R. 1994a. Mice lacking brain-derived neurotrophic factor develop with sensory deficits. Nature 368: 147150.
  • Ernfors P, Lee KF, Kucera J, Jaenisch R. 1994b. Lack of neurotrophin-3 leads to deficiencies in the peripheral nervous system and loss of limb proprioceptive afferents. Cell 77: 503512.
  • Gerard M, Hernandez L, Wevrick R, Stewart C. 1999. Disruption of the mouse necdin gene results in early postnatal lethality: a model for neonatal distress in Prader-Willi syndrome. Nat Genet 23: 199202.
  • Goldstone AP. 2004. Prader-Willi syndrome: advances in genetics, pathophysiology and treatment. Trends Endocrinol Metab 15: 1220.
  • Goridis C, Rohrer H. 2002. Specification of catecholaminergic and serotonergic neurons. Nat Rev Neurosci 3: 531541.
  • Hart PS. 1998. Salivary abnormalities in Prader-Willi syndrome. Ann N Y Acad Sci 842: 125131.
  • Jay P, Rougeulle C, Massacrier A, Moncla A, Mattei MG, Malzac P, Roeckel N, Taviaux S, Lefranc JL, Cau P, Berta P, Lalande M, Muscatelli F. 1997. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nat Genet 17: 357361.
  • Kendall SE, Goldhawk DE, Kubu C, Barker PA, Verdi JM. 2002. Expression analysis of a novel p75(NTR) signaling protein, which regulates cell cycle progression and apoptosis. Mech Dev 117: 187200.
  • Kim JC, Badano JL, Sibold S, Esmail MA, Hill J, Hoskins BE, Leitch CC, Venner K, Ansley SJ, Ross AJ, Leroux MR, Katsanis N, Beales PL. 2004. The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. Nat Genet 36: 462470.
  • Kobayashi M, Taniura H, Yoshikawa K. 2002. Ectopic expression of necdin induces differentiation of mouse neuroblastoma cells. J Biol Chem 277: 4212842135.
  • Kurita M, Kuwajima T, Nishimura I, Yoshikawa K. 2006. Necdin downregulates CDC2 expression to attenuate neuronal apoptosis. J Neurosci 26: 1200312013.
  • Kuruvilla R, Zweifel LS, Glebova NO, Lonze BE, Valdez G, Ye H, Ginty DD. 2004. A neurotrophin signaling cascade coordinates sympathetic neuron development through differential control of TrkA trafficking and retrograde signaling. Cell 118: 243255.
  • Kuwajima T, Taniura H, Nishimura I, Yoshikawa K. 2004. Necdin interacts with the Msx2 homeodomain protein via MAGE-D1 to promote myogenic differentiation of C2C12 cells. J Biol Chem.
  • Kuwako K, Hosokawa A, Nishimura I, Uetsuki T, Yamada M, Nada S, Okada M, Yoshikawa K. 2005. Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival. J Neurosci 25: 70907099.
  • Lee S, Kozlov S, Hernandez L, Chamberlain SJ, Brannan CI, Stewart CL, Wevrick R. 2000. Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype. Hum Mol Genet 9: 18131819.
  • Lee S, Walker CL, Wevrick R. 2003. Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Gene Expr Patterns 3: 599609.
  • Lee S, Walker CL, Karten B, Kuny SL, Tennese AA, O'Neill MA, Wevrick R. 2005. Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth. Hum Mol Genet 14: 627637.
  • MacDonald HR, Wevrick R. 1997. The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum Mol Genet 6: 18731878.
  • Muscatelli F, Abrous DN, Massacrier A, Boccaccio I, Moal ML, Cau P, Cremer H. 2000. Disruption of the mouse necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. Hum Mol Genet 9: 31013110.
  • Nishino J, Mochida K, Ohfuji Y, Shimazaki T, Meno C, Ohishi S, Matsuda Y, Fujii H, Saijoh Y, Hamada H. 1999. GFR alpha3, a component of the artemin receptor, is required for migration and survival of the superior cervical ganglion. Neuron 23: 725736.
  • Pagliardini S, Ren J, Wevrick R, Greer JJ. 2005. Developmental abnormalities of neuronal structure and function in prenatal mice lacking the Prader-Willi syndrome gene necdin. Am J Pathol 167: 175191.
  • Ren J, Lee S, Pagliardini S, Gerard M, Stewart CL, Greer JJ, Wevrick R. 2003. Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice. J Neurosci 23: 15691573.
  • Salehi AH, Roux PP, Kubu CJ, Zeindler C, Bhakar A, Tannis LL, Verdi JM, Barker PA. 2000. NRAGE, a novel MAGE protein, interacts with the p75 neurotrophin receptor and facilitates nerve growth factor-dependent apoptosis. Neuron 27: 279288.
  • Salehi AH, Xanthoudakis S, Barker PA. 2002. NRAGE, a p75 neurotrophin receptor-interacting protein, induces caspase activation and cell death through a JNK-dependent mitochondrial pathway. J Biol Chem 277: 4804348050.
  • Stevenson DA, Anaya TM, Clayton-Smith J, Hall BD, Van Allen MI, Zori RT, Zackai EH, Frank G, Clericuzio CL. 2004. Unexpected death and critical illness in Prader-Willi syndrome: report of ten individuals. Am J Med Genet 124A: 158164.
  • Sutcliffe JS, Han M, Christian SL, Ledbetter DH. 1997. Neuronally-expressed necdin gene: an imprinted candidate gene in Prader- Willi syndrome. Lancet 350: 15201521.
  • Takazaki R, Nishimura I, Yoshikawa K. 2002. Necdin is required for terminal differentiation and survival of primary dorsal root ganglion neurons. Exp Cell Res 277: 220232.
  • Tcherpakov M, Bronfman FC, Conticello SG, Vaskovsky A, Levy Z, Niinobe M, Yoshikawa K, Arenas E, Fainzilber M. 2002. The p75 neurotrophin receptor interacts with multiple MAGE proteins. J Biol Chem 277: 4910149104.
  • Tsai TF, Armstrong D, Beaudet AL. 1999. Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome. Nat Genet 22: 1516.
  • Wharton RH, Bresnan MJ. 1989. Neonatal respiratory depression and delay in diagnosis in Prader-Willi syndrome. Dev Med Child Neurol 31: 231236.