메뉴 건너뛰기




Volumn 9, Issue 9, 2013, Pages

Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional Consequences

Author keywords

[No Author keywords available]

Indexed keywords

NECDIN;

EID: 84884695639     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1003752     Document Type: Article
Times cited : (29)

References (52)
  • 1
    • 0035234557 scopus 로고    scopus 로고
    • Genomic imprintig: parental influence on the genome
    • Reik W, Walter J, (2001) Genomic imprintig: parental influence on the genome. Genetics 2: 21-32.
    • (2001) Genetics , vol.2 , pp. 21-32
    • Reik, W.1    Walter, J.2
  • 2
    • 84864689053 scopus 로고    scopus 로고
    • A survey of tissue-specific genomic imprinting in mammals
    • Prickett AR, Oakey RJ, (2012) A survey of tissue-specific genomic imprinting in mammals. Mol Genet Genomics 287: 621-630.
    • (2012) Mol Genet Genomics , vol.287 , pp. 621-630
    • Prickett, A.R.1    Oakey, R.J.2
  • 3
    • 33947310031 scopus 로고    scopus 로고
    • Environmental epigenomics and disease susceptibility
    • Jirtle RL, Skinner MK, (2007) Environmental epigenomics and disease susceptibility. Nat Rev Genet 8: 253-262.
    • (2007) Nat Rev Genet , vol.8 , pp. 253-262
    • Jirtle, R.L.1    Skinner, M.K.2
  • 4
    • 4444375162 scopus 로고    scopus 로고
    • Selective loss of imprinting in the placenta following preimplantation development in culture
    • Mann MR, Lee SS, Doherty AS, Verona RI, Nolen LD, et al. (2004) Selective loss of imprinting in the placenta following preimplantation development in culture. Development 131: 3727-3735.
    • (2004) Development , vol.131 , pp. 3727-3735
    • Mann, M.R.1    Lee, S.S.2    Doherty, A.S.3    Verona, R.I.4    Nolen, L.D.5
  • 5
    • 77049109156 scopus 로고    scopus 로고
    • Genomic imprinting effects in a compromised in utero environment: implications for a healthy pregnancy
    • Lim AL, Ferguson-Smith AC, (2010) Genomic imprinting effects in a compromised in utero environment: implications for a healthy pregnancy. Semin Cell Dev Biol 21: 201-208.
    • (2010) Semin Cell Dev Biol , vol.21 , pp. 201-208
    • Lim, A.L.1    Ferguson-Smith, A.C.2
  • 6
    • 16944363776 scopus 로고    scopus 로고
    • The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
    • Jay P, Rougeulle C, Massacrier A, Moncla A, Mattei MG, et al. (1997) The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Nat Genet 17: 357-361.
    • (1997) Nat Genet , vol.17 , pp. 357-361
    • Jay, P.1    Rougeulle, C.2    Massacrier, A.3    Moncla, A.4    Mattei, M.G.5
  • 7
    • 0030776554 scopus 로고    scopus 로고
    • The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region
    • Watrin F, Roeckel N, Lacroix L, Mignon C, Mattei MG, et al. (1997) The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region. Eur J Hum Genet 5: 324-332.
    • (1997) Eur J Hum Genet , vol.5 , pp. 324-332
    • Watrin, F.1    Roeckel, N.2    Lacroix, L.3    Mignon, C.4    Mattei, M.G.5
  • 8
    • 0030773594 scopus 로고    scopus 로고
    • The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse
    • 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: 1873-1878.
    • (1997) Hum Mol Genet , vol.6 , pp. 1873-1878
    • MacDonald, H.R.1    Wevrick, R.2
  • 9
    • 0345062183 scopus 로고    scopus 로고
    • Disruption of the mouse necdin gene results in early post-natal lethality
    • Gerard M, Hernandez L, Wevrick R, Stewart CL, (1999) Disruption of the mouse necdin gene results in early post-natal lethality. Nat Genet 23: 199-202.
    • (1999) Nat Genet , vol.23 , pp. 199-202
    • Gerard, M.1    Hernandez, L.2    Wevrick, R.3    Stewart, C.L.4
  • 10
    • 77952885487 scopus 로고    scopus 로고
    • Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13
    • Chamberlain SJ, Lalande M, (2010) Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13. Neurobiol Dis 39: 13-20.
    • (2010) Neurobiol Dis , vol.39 , pp. 13-20
    • Chamberlain, S.J.1    Lalande, M.2
  • 12
    • 79956282385 scopus 로고    scopus 로고
    • Prader-Willi Syndrome: Obesity due to Genomic Imprinting
    • Butler MG, (2011) Prader-Willi Syndrome: Obesity due to Genomic Imprinting. Curr Genomics 12: 204-215.
    • (2011) Curr Genomics , vol.12 , pp. 204-215
    • Butler, M.G.1
  • 13
    • 79951679866 scopus 로고    scopus 로고
    • Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding
    • McAllister CJ, Whittington JE, Holland AJ, (2011) Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding. Int J Obes (Lond) 35: 188-197.
    • (2011) Int J Obes (Lond) , vol.35 , pp. 188-197
    • McAllister, C.J.1    Whittington, J.E.2    Holland, A.J.3
  • 14
    • 80052376047 scopus 로고    scopus 로고
    • Prader-Willi syndrome and autism spectrum disorders: an evolving story
    • Dykens EM, Lee E, Roof E, (2011) Prader-Willi syndrome and autism spectrum disorders: an evolving story. J Neurodev Disord 3: 225-237.
    • (2011) J Neurodev Disord , vol.3 , pp. 225-237
    • Dykens, E.M.1    Lee, E.2    Roof, E.3
  • 15
    • 33845472885 scopus 로고    scopus 로고
    • Sleep-related breathing disorders in pre-pubertal children with Prader-Willi Syndrome and effects of growth hormone treatment
    • Festen DA, de Weerd AW, van den Bossche RA, Joosten K, Hoeve H, et al. (2006) Sleep-related breathing disorders in pre-pubertal children with Prader-Willi Syndrome and effects of growth hormone treatment. J Clin Endocrinol Metab 91: 4911-5.
    • (2006) J Clin Endocrinol Metab , vol.91 , pp. 4911-4915
    • Festen, D.A.1    de Weerd, A.W.2    van den Bossche, R.A.3    Joosten, K.4    Hoeve, H.5
  • 16
    • 41849091898 scopus 로고    scopus 로고
    • Review of 64 cases of death in children with Prader-Willi syndrome (PWS)
    • Tauber M, Diene G, Molinas C, Hebert M, (2008) Review of 64 cases of death in children with Prader-Willi syndrome (PWS). Am J Med Genet A 146: 881-887.
    • (2008) Am J Med Genet A , vol.146 , pp. 881-887
    • Tauber, M.1    Diene, G.2    Molinas, C.3    Hebert, M.4
  • 17
    • 0034642301 scopus 로고    scopus 로고
    • Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome
    • Muscatelli F, Abrous DN, Massacrier A, Boccaccio I, Le Moal M, et al. (2000) Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. Hum Mol Genet 9: 3101-3110.
    • (2000) Hum Mol Genet , vol.9 , pp. 3101-3110
    • Muscatelli, F.1    Abrous, D.N.2    Massacrier, A.3    Boccaccio, I.4    Le Moal, M.5
  • 18
    • 0032963667 scopus 로고    scopus 로고
    • Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome [letter]
    • Tsai TF, Armstrong D, Beaudet AL, (1999) Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome [letter]. Nat Genet 22: 15-16.
    • (1999) Nat Genet , vol.22 , pp. 15-16
    • Tsai, T.F.1    Armstrong, D.2    Beaudet, A.L.3
  • 19
    • 23044445639 scopus 로고    scopus 로고
    • Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival
    • Kuwako K, Hosokawa A, Nishimura I, Uetsuki T, Yamada M, et al. (2005) Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival. J Neurosci 25: 7090-7099.
    • (2005) J Neurosci , vol.25 , pp. 7090-7099
    • Kuwako, K.1    Hosokawa, A.2    Nishimura, I.3    Uetsuki, T.4    Yamada, M.5
  • 20
    • 0037335439 scopus 로고    scopus 로고
    • Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice
    • Ren J, Lee S, Pagliardini S, Gerard M, Stewart CL, et al. (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: 1569-1573.
    • (2003) J Neurosci , vol.23 , pp. 1569-1573
    • Ren, J.1    Lee, S.2    Pagliardini, S.3    Gerard, M.4    Stewart, C.L.5
  • 21
    • 33751581604 scopus 로고    scopus 로고
    • Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death
    • Andrieu D, Meziane H, Marly F, Angelats C, Fernandez PA, et al. (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: 56.
    • (2006) BMC Dev Biol , vol.6 , pp. 56
    • Andrieu, D.1    Meziane, H.2    Marly, F.3    Angelats, C.4    Fernandez, P.A.5
  • 22
    • 39549109269 scopus 로고    scopus 로고
    • Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome
    • Zanella S, Watrin F, Mebarek S, Marly F, Roussel M, et al. (2008) Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome. J Neurosci 28: 1745-1755.
    • (2008) J Neurosci , vol.28 , pp. 1745-1755
    • Zanella, S.1    Watrin, F.2    Mebarek, S.3    Marly, F.4    Roussel, M.5
  • 23
    • 77249114260 scopus 로고    scopus 로고
    • Variability in gene expression underlies incomplete penetrance
    • Raj A, Rifkin SA, Andersen E, van Oudenaarden A, (2010) Variability in gene expression underlies incomplete penetrance. Nature 463: 913-918.
    • (2010) Nature , vol.463 , pp. 913-918
    • Raj, A.1    Rifkin, S.A.2    Andersen, E.3    van Oudenaarden, A.4
  • 24
    • 0344876548 scopus 로고    scopus 로고
    • Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression
    • Andrieu D, Watrin F, Niinobe M, Yoshikawa K, Muscatelli F, et al. (2003) Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression. Gene Expr Patterns 3: 761-765.
    • (2003) Gene Expr Patterns , vol.3 , pp. 761-765
    • Andrieu, D.1    Watrin, F.2    Niinobe, M.3    Yoshikawa, K.4    Muscatelli, F.5
  • 25
    • 77954909570 scopus 로고    scopus 로고
    • Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns
    • Schneider E, Pliushch G, El Hajj N, Galetzka D, Puhl A, et al. (2010) Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns. Nucleic Acids Res 38: 3880-3890.
    • (2010) Nucleic Acids Res , vol.38 , pp. 3880-3890
    • Schneider, E.1    Pliushch, G.2    El Hajj, N.3    Galetzka, D.4    Puhl, A.5
  • 26
    • 0035102797 scopus 로고    scopus 로고
    • Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center
    • Hanel ML, Wevrick R, (2001) Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center. Mol Cell Biol 21: 2384-2392.
    • (2001) Mol Cell Biol , vol.21 , pp. 2384-2392
    • Hanel, M.L.1    Wevrick, R.2
  • 28
    • 0032406308 scopus 로고    scopus 로고
    • Relaxation of imprinting in Prader-Willi syndrome [In Process Citation]
    • Rogan PK, Seip JR, White LM, Wenger SL, Steele MW, et al. (1998) Relaxation of imprinting in Prader-Willi syndrome [In Process Citation]. Hum Genet 103: 694-701.
    • (1998) Hum Genet , vol.103 , pp. 694-701
    • Rogan, P.K.1    Seip, J.R.2    White, L.M.3    Wenger, S.L.4    Steele, M.W.5
  • 29
    • 0033123473 scopus 로고    scopus 로고
    • Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities
    • Muralidhar B, Marney A, Butler MG, (1999) Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities. Genet Med 1: 141-145.
    • (1999) Genet Med , vol.1 , pp. 141-145
    • Muralidhar, B.1    Marney, A.2    Butler, M.G.3
  • 30
    • 33846581497 scopus 로고    scopus 로고
    • Loss of imprinting and cancer
    • Jelinic P, Shaw P, (2007) Loss of imprinting and cancer. J Pathol 211: 261-268.
    • (2007) J Pathol , vol.211 , pp. 261-268
    • Jelinic, P.1    Shaw, P.2
  • 31
    • 84874323462 scopus 로고    scopus 로고
    • The secret language of destiny: stress imprinting and transgenerational origins of disease
    • Zucchi FC, Yao Y, Metz GA, (2012) The secret language of destiny: stress imprinting and transgenerational origins of disease. Front Genet 3: 96.
    • (2012) Front Genet , vol.3 , pp. 96
    • Zucchi, F.C.1    Yao, Y.2    Metz, G.A.3
  • 32
    • 49749114829 scopus 로고    scopus 로고
    • Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain
    • Xu J, Deng X, Disteche CM, (2008) Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain. PLoS One 3: e2553.
    • (2008) PLoS One , vol.3
    • Xu, J.1    Deng, X.2    Disteche, C.M.3
  • 33
    • 77449137288 scopus 로고    scopus 로고
    • Explaining inter-individual variability in phenotype: is epigenetics up to the challenge
    • Turan N, Katari S, Coutifaris C, Sapienza C, (2010) Explaining inter-individual variability in phenotype: is epigenetics up to the challenge? Epigenetics 5: 16-19.
    • (2010) Epigenetics , vol.5 , pp. 16-19
    • Turan, N.1    Katari, S.2    Coutifaris, C.3    Sapienza, C.4
  • 34
    • 84862809133 scopus 로고    scopus 로고
    • The association between oxytocin receptor gene polymorphism (OXTR) and trait empathy
    • Wu N, Li Z, Su Y, (2012) The association between oxytocin receptor gene polymorphism (OXTR) and trait empathy. J Affect Disord 138: 468-472.
    • (2012) J Affect Disord , vol.138 , pp. 468-472
    • Wu, N.1    Li, Z.2    Su, Y.3
  • 35
    • 33644557773 scopus 로고    scopus 로고
    • Transient homologous chromosome pairing marks the onset of X inactivation
    • Xu N, Tsai CL, Lee JT, (2006) Transient homologous chromosome pairing marks the onset of X inactivation. Science 311: 1149-1152.
    • (2006) Science , vol.311 , pp. 1149-1152
    • Xu, N.1    Tsai, C.L.2    Lee, J.T.3
  • 36
    • 15544382113 scopus 로고    scopus 로고
    • Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples
    • Thatcher KN, Peddada S, Yasui DH, Lasalle JM, (2005) Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples. Hum Mol Genet 14: 785-797.
    • (2005) Hum Mol Genet , vol.14 , pp. 785-797
    • Thatcher, K.N.1    Peddada, S.2    Yasui, D.H.3    Lasalle, J.M.4
  • 37
    • 84863632595 scopus 로고    scopus 로고
    • Pairing of homologous regions in the mouse genome is associated with transcription but not imprinting status
    • Krueger C, King MR, Krueger F, Branco MR, Osborne CS, et al. (2012) Pairing of homologous regions in the mouse genome is associated with transcription but not imprinting status. PLoS ONE 7: e38983.
    • (2012) PLoS ONE , vol.7
    • Krueger, C.1    King, M.R.2    Krueger, F.3    Branco, M.R.4    Osborne, C.S.5
  • 38
    • 84858439862 scopus 로고    scopus 로고
    • Insights into the regulation of protein abundance from proteomic and transcriptomic analyses
    • Vogel C, Marcotte EM, (2012) Insights into the regulation of protein abundance from proteomic and transcriptomic analyses. Nat Rev Genet 13: 227-232.
    • (2012) Nat Rev Genet , vol.13 , pp. 227-232
    • Vogel, C.1    Marcotte, E.M.2
  • 39
    • 79960633906 scopus 로고    scopus 로고
    • Regulatory mechanisms and networks couple the different phases of gene expression
    • Dahan O, Gingold H, Pilpel Y, (2011) Regulatory mechanisms and networks couple the different phases of gene expression. Trends Genet 27: 316-322.
    • (2011) Trends Genet , vol.27 , pp. 316-322
    • Dahan, O.1    Gingold, H.2    Pilpel, Y.3
  • 40
    • 84858414016 scopus 로고    scopus 로고
    • Regulated noise in the epigenetic landscape of development and disease
    • Pujadas E, Feinberg AP, (2012) Regulated noise in the epigenetic landscape of development and disease. Cell 148: 1123-1131.
    • (2012) Cell , vol.148 , pp. 1123-1131
    • Pujadas, E.1    Feinberg, A.P.2
  • 42
    • 33747780450 scopus 로고    scopus 로고
    • Unexpected expression of orexin-B in basal conditions and increased levels in the adult rat hippocampus during pilocarpine-induced epileptogenesis
    • Morales A, Bonnet C, Bourgoin N, Touvier T, Nadam J, et al. (2006) Unexpected expression of orexin-B in basal conditions and increased levels in the adult rat hippocampus during pilocarpine-induced epileptogenesis. Brain Res 1109: 164-175.
    • (2006) Brain Res , vol.1109 , pp. 164-175
    • Morales, A.1    Bonnet, C.2    Bourgoin, N.3    Touvier, T.4    Nadam, J.5
  • 43
    • 25444531466 scopus 로고    scopus 로고
    • The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene
    • Watrin F, Le Meur E, Roeckel N, Ripoche MA, Dandolo L, et al. (2005) The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene. BMC Genet 6: 1.
    • (2005) BMC Genet , vol.6 , pp. 1
    • Watrin, F.1    Le Meur, E.2    Roeckel, N.3    Ripoche, M.A.4    Dandolo, L.5
  • 44
    • 35448978427 scopus 로고    scopus 로고
    • Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human
    • Ruf N, Bahring S, Galetzka D, Pliushch G, Luft FC, et al. (2007) Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human. Hum Mol Genet 16: 2591-2599.
    • (2007) Hum Mol Genet , vol.16 , pp. 2591-2599
    • Ruf, N.1    Bahring, S.2    Galetzka, D.3    Pliushch, G.4    Luft, F.C.5
  • 45
    • 0025861818 scopus 로고
    • Detection of specific polymerase chain reaction product by utilizing the 5′--3′ exonuclease activity of Thermus aquaticus DNA polymerase
    • Holland PM, Abramson RD, Watson R, Gelfand DH, (1991) Detection of specific polymerase chain reaction product by utilizing the 5′--3′ exonuclease activity of Thermus aquaticus DNA polymerase. Proc Natl Acad Sci U S A 88: 7276-7280.
    • (1991) Proc Natl Acad Sci U S A , vol.88 , pp. 7276-7280
    • Holland, P.M.1    Abramson, R.D.2    Watson, R.3    Gelfand, D.H.4
  • 46
    • 0033006003 scopus 로고    scopus 로고
    • Allelic discrimination using fluorogenic probes and the 5′ nuclease assay
    • Livak KJ, (1999) Allelic discrimination using fluorogenic probes and the 5′ nuclease assay. Genet Anal 14: 143-149.
    • (1999) Genet Anal , vol.14 , pp. 143-149
    • Livak, K.J.1
  • 48
    • 0030471926 scopus 로고    scopus 로고
    • A modified and improved method for bisulphite based cytosine methylation analysis
    • Olek A, Oswald J, Walter J, (1996) A modified and improved method for bisulphite based cytosine methylation analysis. Nucleic Acids Res 24: 5064-5066.
    • (1996) Nucleic Acids Res , vol.24 , pp. 5064-5066
    • Olek, A.1    Oswald, J.2    Walter, J.3
  • 49
    • 0036911371 scopus 로고    scopus 로고
    • Highly efficient modification of bacterial artificial chromosomes (BACs) using novel shuttle vectors containing the R6Kgamma origin of replication
    • Gong S, Yang XW, Li C, Heintz N, (2002) Highly efficient modification of bacterial artificial chromosomes (BACs) using novel shuttle vectors containing the R6Kgamma origin of replication. Genome Res 12: 1992-1998.
    • (2002) Genome Res , vol.12 , pp. 1992-1998
    • Gong, S.1    Yang, X.W.2    Li, C.3    Heintz, N.4
  • 50
    • 84861184163 scopus 로고    scopus 로고
    • Neuronal histamine production remains unaltered in Parkinson's disease despite the accumulation of Lewy bodies and Lewy neurites in the tuberomamillary nucleus
    • Shan L, Liu CQ, Balesar R, Hofman MA, Bao AM, et al. (2012) Neuronal histamine production remains unaltered in Parkinson's disease despite the accumulation of Lewy bodies and Lewy neurites in the tuberomamillary nucleus. Neurobiol Aging 33: 1343-1344.
    • (2012) Neurobiol Aging , vol.33 , pp. 1343-1344
    • Shan, L.1    Liu, C.Q.2    Balesar, R.3    Hofman, M.A.4    Bao, A.M.5
  • 51
    • 0032402062 scopus 로고    scopus 로고
    • Evidence for a role of the chemorepellent semaphorin III and its receptor neuropilin-1 in the regeneration of primary olfactory axons
    • Pasterkamp RJ, De Winter F, Holtmaat AJ, Verhaagen J, (1998) Evidence for a role of the chemorepellent semaphorin III and its receptor neuropilin-1 in the regeneration of primary olfactory axons. J Neurosci 18: 9962-9976.
    • (1998) J Neurosci , vol.18 , pp. 9962-9976
    • Pasterkamp, R.J.1    De Winter, F.2    Holtmaat, A.J.3    Verhaagen, J.4
  • 52
    • 20244388118 scopus 로고    scopus 로고
    • Increased melanin concentrating hormone receptor type I in the human hypothalamic infundibular nucleus in cachexia
    • Unmehopa UA, van Heerikhuize JJ, Spijkstra W, Woods JW, Howard AD, et al. (2005) Increased melanin concentrating hormone receptor type I in the human hypothalamic infundibular nucleus in cachexia. J Clin Endocrinol Metab 90: 2412-2419.
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 2412-2419
    • Unmehopa, U.A.1    van Heerikhuize, J.J.2    Spijkstra, W.3    Woods, J.W.4    Howard, A.D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.