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Volumn 14, Issue 1, 2013, Pages 2-10

Invertebrate models of Kallmann Syndrome: Molecular pathogenesis and new disease genes

Author keywords

Animal models; Axon branching; CeKal 1; DmKal 1; Extracellular matrix; Morphogenesis

Indexed keywords

ANOSMIN 1; CHROMODOMAIN HELICASE DNA BINDING PROTEIN 7; FIBROBLAST GROWTH FACTOR 8; FIBROBLAST GROWTH FACTOR RECEPTOR 1; FIBRONECTIN; FIBRONECTIN III; GROWTH FACTOR RECEPTOR; PROKINETICIN 2; PROKINETICIN 2 RECEPTOR; PROTEINS AND PEPTIDES; PROTEOHEPARAN SULFATE; UNCLASSIFIED DRUG; WHEY ACIDIC PROTEIN;

EID: 84888218718     PISSN: 13892029     EISSN: 18755488     Source Type: Journal    
DOI: 10.2174/138920213804999174     Document Type: Review
Times cited : (17)

References (69)
  • 1
  • 4
    • 0017828707 scopus 로고
    • Hereditary bimanual synkinesis combined with hypogonadotropic hypogonadism and anosmia in four brothers
    • Conrad, B.; Kriebel, J.; Hetzel, W. D., Hereditary bimanual synkinesis combined with hypogonadotropic hypogonadism and anosmia in four brothers. J Neurol 1978, 218 (4), 263-274.
    • (1978) J Neurol , vol.218 , Issue.4 , pp. 263-274
    • Conrad, B.1    Kriebel, J.2    Hetzel, W.D.3
  • 5
    • 0022256144 scopus 로고
    • Heterogeneity of Kallmann's syndrome
    • Hermanussen, M.; Sippell, W. G., Heterogeneity of Kallmann's syndrome. Clin Genet 1985, 28 (2), 106-111.
    • (1985) Clin Genet , vol.28 , Issue.2 , pp. 106-111
    • Hermanussen, M.1    Sippell, W.G.2
  • 6
    • 0014299727 scopus 로고
    • Familial hypogonado tropic hypogonadism with anosmia
    • Sparkes, R. S.; Simpson, R. W.; CA, P., Familial hypogonado tropic hypogonadism with anosmia. Arch Intern Med 1968, 121 (6), 534-538.
    • (1968) Arch Intern Med , vol.121 , Issue.6 , pp. 534-538
    • Sparkes, R.S.1    Simpson, R.W.2    Ca, P.3
  • 7
    • 0020554722 scopus 로고
    • The syndrome of anosmia with hypogonadotropic hypogona dism: A genetic study of 18 new families and a review
    • White, B. J.; Rogol, A. D.; Brown, K. S.; Lieblich, J. M.; Rosen, S. W., The syndrome of anosmia with hypogonadotropic hypogona dism: a genetic study of 18 new families and a review. Am J Med Genet 1983, 15 (3), 417-435.
    • (1983) Am J Med Genet , vol.15 , Issue.3 , pp. 417-435
    • White, B.J.1    Rogol, A.D.2    Brown, K.S.3    Lieblich, J.M.4    Rosen, S.W.5
  • 8
    • 0023800035 scopus 로고
    • Mode of inheritance in familial cases of primary gonado tropic deficiency
    • Chaussain, J. L.; Toublanc, J. E.; Feingold, J.; Naud, C.; Vassal, J.; Job, J. C., Mode of inheritance in familial cases of primary gonado tropic deficiency. Horm Res 1988, 29 (5-6), 202-206.
    • (1988) Horm Res , vol.29 , Issue.5-6 , pp. 202-206
    • Chaussain, J.L.1    Toublanc, J.E.2    Feingold, J.3    Naud, C.4    Vassal, J.5    Job, J.C.6
  • 9
    • 0024470630 scopus 로고
    • Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome
    • Schwanzel-Fukuda, M.; Bick, D.; Pfaff, D. W., Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome. Brain Res Mol Brain Res 1989, 6 (4), 311-326.
    • (1989) Brain Res Mol Brain Res , vol.6 , Issue.4 , pp. 311-326
    • Schwanzel-Fukuda, M.1    Bick, D.2    Pfaff, D.W.3
  • 10
    • 0027478174 scopus 로고
    • Expression of the KAL gene in multiple neuronal sites during chicken development
    • Legouis, R.; Lievre, C. A.; Leibovici, M.; Lapointe, F.; Petit, C., Expression of the KAL gene in multiple neuronal sites during chicken development. Proc Natl Acad Sci U S A 1993, 90 (6), 2461-2465.
    • (1993) Proc Natl Acad Sci U S A , vol.90 , Issue.6 , pp. 2461-2465
    • Legouis, R.1    Lievre, C.A.2    Leibovici, M.3    Lapointe, F.4    Petit, C.5
  • 11
    • 0027264925 scopus 로고
    • X-linked Kallmann syndrome. A neuronal targeting defect in the olfactory system?
    • Lutz, B.; Rugarli, E. I.; Eichele, G.; Ballabio, A., X-linked Kallmann syndrome. A neuronal targeting defect in the olfactory system? FEBS Lett 1993, 325 (1-2), 128-134.
    • (1993) FEBS Lett , vol.325 , Issue.1-2 , pp. 128-134
    • Lutz, B.1    Rugarli, E.I.2    Eichele, G.3    Ballabio, A.4
  • 13
    • 0036549115 scopus 로고    scopus 로고
    • GnRH neuronal development: Insights into hypogonadotrophic hypogonadism
    • MacColl, G.; Quinton, R.; Bouloux, P. M., GnRH neuronal development: insights into hypogonadotrophic hypogonadism. Trends Endocrinol Metab 2002, 13 (3), 112-118.
    • (2002) Trends Endocrinol Metab , vol.13 , Issue.3 , pp. 112-118
    • McColl, G.1    Quinton, R.2    Bouloux, P.M.3
  • 14
    • 0027319774 scopus 로고
    • MR imaging of Kallmann syndrome, a genetic disorder of neuronal migration affecting the olfactory and genital systems
    • Truwit, C. L.; Barkovich, A. J.; Grumbach, M. M.; Martini, J. J., MR imaging of Kallmann syndrome, a genetic disorder of neuronal migration affecting the olfactory and genital systems. AJNR Am J Neuroradiol 1993, 14 (4), 827-838.
    • (1993) AJNR Am J Neuroradiol , vol.14 , Issue.4 , pp. 827-838
    • Truwit, C.L.1    Barkovich, A.J.2    Grumbach, M.M.3    Martini, J.J.4
  • 15
    • 33750902966 scopus 로고    scopus 로고
    • Kallmann's syndrome, a neuronal migra tion defect
    • Cariboni, A.; Maggi, R., Kallmann's syndrome, a neuronal migra tion defect. Cellular and Molecular Life Sciences 2006, 63 (21), 2512-2526.
    • (2006) Cellular and Molecular Life Sciences , vol.63 , Issue.21 , pp. 2512-2526
    • Cariboni, A.1    Maggi, R.2
  • 16
    • 80053383830 scopus 로고    scopus 로고
    • X-linked GnRH deficiency: Role of KAL-1 mutations in GnRH deficiency
    • Hu, Y. L.; Bouloux, P. M., X-linked GnRH deficiency: Role of KAL-1 mutations in GnRH deficiency. Molecular and Cellular Endocrinology 2011, 346 (1-2), 13-20.
    • (2011) Molecular and Cellular Endocrinology , vol.346 , Issue.1-2 , pp. 13-20
    • Hu, Y.L.1    Bouloux, P.M.2
  • 19
    • 0020489775 scopus 로고
    • Mouse whey acidic protein is a novel member of the family of 'four-disulfide core' proteins
    • Hennighausen, L. G.; Sippel, A. E., Mouse whey acidic protein is a novel member of the family of 'four-disulfide core' proteins. Nucleic Acids Res 1982, 10 (8), 2677-2684.
    • (1982) Nucleic Acids Res , vol.10 , Issue.8 , pp. 2677-2684
    • Hennighausen, L.G.1    Sippel, A.E.2
  • 20
    • 0019996137 scopus 로고
    • Complete sequence analysis of cDNA clones encoding rat whey phosphoprotein: Homology to a protease inhibitor
    • Dandekar, A. M.; Robinson, E. A.; Appella, E.; Qasba, P. K., Complete sequence analysis of cDNA clones encoding rat whey phosphoprotein: homology to a protease inhibitor. Proc Natl Acad Sci U S A 1982, 79 (13), 3987-3991.
    • (1982) Proc Natl Acad Sci U S A , vol.79 , Issue.13 , pp. 3987-3991
    • Dandekar, A.M.1    Robinson, E.A.2    Appella, E.3    Qasba, P.K.4
  • 21
    • 0024513886 scopus 로고
    • Understanding the molecules of neural cell contacts: Emerging patterns of structure and function
    • Lander, A. D., Understanding the molecules of neural cell contacts: emerging patterns of structure and function. Trends Neurosci 1989, 12 (5), 189-195.
    • (1989) Trends Neurosci , vol.12 , Issue.5 , pp. 189-195
    • Lander, A.D.1
  • 22
    • 0025817934 scopus 로고
    • Cell adhesion molecules: Implications for a molecular histology
    • Edelman, G. M.; Crossin, K. L., Cell adhesion molecules: implications for a molecular histology. Annu Rev Biochem 1991, 60, 155-190.
    • (1991) Annu Rev Biochem , vol.60 , pp. 155-190
    • Edelman, G.M.1    Crossin, K.L.2
  • 26
    • 58349117694 scopus 로고    scopus 로고
    • Kallmann syndrome
    • Dode, C.; Hardelin, J. P., Kallmann syndrome. Eur J Hum Genet 2009, 17 (2), 139-146.
    • (2009) Eur J Hum Genet , vol.17 , Issue.2 , pp. 139-146
    • Dode, C.1    Hardelin, J.P.2
  • 27
    • 55749108383 scopus 로고    scopus 로고
    • The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al
    • Hardelin, J. P.; Dode, C., The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al. Sex Dev 2008, 2 (4-5), 181-193.
    • (2008) Sex Dev , vol.2 , Issue.4-5 , pp. 181-193
    • Hardelin, J.P.1    Dode, C.2
  • 29
    • 11144249928 scopus 로고    scopus 로고
    • Kallmann syndrome: Fibroblast growth factor signaling insufficiency?
    • Dode, C.; Hardelin, J. P., Kallmann syndrome: fibroblast growth factor signaling insufficiency? Journal of Molecular Medicine-Jmm 2004, 82 (11), 725-734.
    • (2004) Journal of Molecular Medicine-Jmm , vol.82 , Issue.11 , pp. 725-734
    • Dode, C.1    Hardelin, J.P.2
  • 36
    • 80053385843 scopus 로고    scopus 로고
    • The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonado tropic hypogonadism and Kallmann syndrome
    • Kim, H. G.; Layman, L. C., The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonado tropic hypogonadism and Kallmann syndrome. Mol Cell Endocri nol 2011, 346 (1-2), 74-83.
    • (2011) Mol Cell Endocri nol , vol.346 , Issue.1-2 , pp. 74-83
    • Kim, H.G.1    Layman, L.C.2
  • 37
    • 80053385954 scopus 로고    scopus 로고
    • Role of fibroblast growth factor (FGF) signaling in the neuroendocrine control of human reproduction
    • Miraoui, H.; Dwyer, A.; Pitteloud, N., Role of fibroblast growth factor (FGF) signaling in the neuroendocrine control of human reproduction. Mol Cell Endocrinol 2011, 346 (1-2), 37-43.
    • (2011) Mol Cell Endocrinol , vol.346 , Issue.1-2 , pp. 37-43
    • Miraoui, H.1    Dwyer, A.2    Pitteloud, N.3
  • 38
    • 79959916267 scopus 로고    scopus 로고
    • Genetic basis and variable phenotypic expression of Kallmann syndrome: Towards a unifying theory
    • Mitchell, A. L.; Dwyer, A.; Pitteloud, N.; Quinton, R., Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory. Trends Endocrinol Metab 2011, 22 (7), 249-258.
    • (2011) Trends Endocrinol Metab , vol.22 , Issue.7 , pp. 249-258
    • Mitchell, A.L.1    Dwyer, A.2    Pitteloud, N.3    Quinton, R.4
  • 40
    • 0031787628 scopus 로고    scopus 로고
    • Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner
    • Soussi-Yanicostas, N.; Faivre-Sarrailh, C.; Hardelin, J. P.; Levilliers, J.; Rougon, G.; Petit, C., Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner. Journal of Cell Science 1998, 111, 2953-2965.
    • (1998) Journal of Cell Science , vol.111 , pp. 2953-2965
    • Soussi-Yanicostas, N.1    Faivre-Sarrailh, C.2    Hardelin, J.P.3    Levilliers, J.4    Rougon, G.5    Petit, C.6
  • 41
    • 9244231594 scopus 로고    scopus 로고
    • Cross-talk of anosmin-1, the protein implicated in X-linked Kallmann's syndrome, with heparan sulphate and urokinase-type plasminogen activator
    • Hu, Y. L.; Gonzalez-Martinez, D.; Kim, S. H.; Bouloux, P. M. G., Cross-talk of anosmin-1, the protein implicated in X-linked Kallmann's syndrome, with heparan sulphate and urokinase-type plasminogen activator. Biochemical Journal 2004, 384, 495-505.
    • (2004) Biochemical Journal , vol.384 , pp. 495-505
    • Hu, Y.L.1    Gonzalez-Martinez, D.2    Kim, S.H.3    Bouloux, P.M.G.4
  • 42
    • 33744969509 scopus 로고    scopus 로고
    • Celegans Kallmann syndrome protein KAL-1 interacts with syndecan and glypican to regulate neuronal cell migrations
    • Hudson, M. L.; Kinnunen, T.; Cinar, H. N.; Chisholm, A. D., Celegans Kallmann syndrome protein KAL-1 interacts with syndecan and glypican to regulate neuronal cell migrations. Developmental Biology 2006, 294 (2), 352-365.
    • (2006) Developmental Biology , vol.294 , Issue.2 , pp. 352-365
    • Hudson, M.L.1    Kinnunen, T.2    Cinar, H.N.3    Chisholm, A.D.4
  • 43
    • 43549086414 scopus 로고    scopus 로고
    • Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR
    • Axang, C.; Rauthan, M.; Hall, D. H.; Pilon, M., Developmental genetics of the C. elegans pharyngeal neurons NSML and NSMR. BMC Dev Biol 2008, 8, 38.
    • (2008) BMC Dev Biol , vol.8 , pp. 38
    • Axang, C.1    Rauthan, M.2    Hall, D.H.3    Pilon, M.4
  • 45
    • 2642542826 scopus 로고    scopus 로고
    • Differential sulfations and epimerization define heparan sulfate specificity in nervous system development
    • Bulow, H. E.; Hobert, O., Differential sulfations and epimerization define heparan sulfate specificity in nervous system development. Neuron 2004, 41 (5), 723-736.
    • (2004) Neuron , vol.41 , Issue.5 , pp. 723-736
    • Bulow, H.E.1    Hobert, O.2
  • 46
    • 71449120985 scopus 로고    scopus 로고
    • The PAPS transporter PST-1 is required for heparan sulfation and is essential for viability and neural development in C. elegans
    • Bhattacharya, R.; Townley, R. A.; Berry, K. L.; Bulow, H. E., The PAPS transporter PST-1 is required for heparan sulfation and is essential for viability and neural development in C. elegans. J Cell Sci 2009, 122 (Pt 24), 4492-4504.
    • (2009) J Cell Sci , vol.122 , Issue.Pt 24 , pp. 4492-4504
    • Bhattacharya, R.1    Townley, R.A.2    Berry, K.L.3    Bulow, H.E.4
  • 47
    • 33751187897 scopus 로고    scopus 로고
    • The molecular diversity of glycosamino glycans shapes animal development
    • Bulow, H. E.; Hobert, O., The molecular diversity of glycosamino glycans shapes animal development. Annu Rev Cell Dev Biol 2006, 22, 375-407.
    • (2006) Annu Rev Cell Dev Biol , vol.22 , pp. 375-407
    • Bulow, H.E.1    Hobert, O.2
  • 48
    • 0027278607 scopus 로고
    • Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting
    • Rugarli, E. I.; Lutz, B.; Kuratani, S. C.; Wawersik, S.; Borsani, G.; Ballabio, A.; Eichele, G., Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting. Nat Genet 1993, 4 (1), 19-26.
    • (1993) Nat Genet , vol.4 , Issue.1 , pp. 19-26
    • Rugarli, E.I.1    Lutz, B.2    Kuratani, S.C.3    Wawersik, S.4    Borsani, G.5    Ballabio, A.6    Eichele, G.7
  • 49
    • 0037351187 scopus 로고    scopus 로고
    • FGF signaling through FGFR1 is required for olfactory bulb morphogenesis
    • Hebert, J. M.; Lin, M.; Partanen, J.; Rossant, J.; McConnell, S. K., FGF signaling through FGFR1 is required for olfactory bulb morphogenesis. Development 2003, 130 (6), 1101-1111.
    • (2003) Development , vol.130 , Issue.6 , pp. 1101-1111
    • Hebert, J.M.1    Lin, M.2    Partanen, J.3    Rossant, J.4    McConnell, S.K.5
  • 51
    • 9244247298 scopus 로고    scopus 로고
    • Anosmin-1 modulates fibroblast growth factor receptor 1 signaling in human gonadotropin-releasing hormone olfactory neuroblasts through a heparan sulfate-dependent mechanism
    • Gonzalez-Martinez, D.; Kim, S. H.; Hu, Y. L.; Guimond, S.; Schofield, J.; Winyard, P.; Vannelli, G. B.; Turnbull, J.; Bouloux, P. M., Anosmin-1 modulates fibroblast growth factor receptor 1 signaling in human gonadotropin-releasing hormone olfactory neuroblasts through a heparan sulfate-dependent mechanism. Journal of Neuroscience 2004, 24 (46), 10384-10392.
    • (2004) Journal of Neuroscience , vol.24 , Issue.46 , pp. 10384-10392
    • Gonzalez-Martinez, D.1    Kim, S.H.2    Hu, Y.L.3    Guimond, S.4    Schofield, J.5    Winyard, P.6    Vannelli, G.B.7    Turnbull, J.8    Bouloux, P.M.9
  • 52
    • 77953358407 scopus 로고    scopus 로고
    • Novel insights in FGFR1 regulation: Lessons from Kallmann syndrome
    • Hu, Y. L.; Bouloux, P. M., Novel insights in FGFR1 regulation: lessons from Kallmann syndrome. Trends in Endocrinology and Metabolism 2010, 21 (6), 385-393.
    • (2010) Trends in Endocrinology and Metabolism , vol.21 , Issue.6 , pp. 385-393
    • Hu, Y.L.1    Bouloux, P.M.2
  • 53
    • 70350398217 scopus 로고    scopus 로고
    • Novel mechanisms of fibroblast growth factor receptor 1 regulation by extracellular matrix protein anosmin-1
    • Hu, Y.; Guimond, S. E.; Travers, P.; Cadman, S.; Hohenester, E.; Turnbull, J. E.; Kim, S. H.; Bouloux, P. M., Novel mechanisms of fibroblast growth factor receptor 1 regulation by extracellular matrix protein anosmin-1. J Biol Chem 2009, 284 (43), 29905-29920.
    • (2009) J Biol Chem , vol.284 , Issue.43 , pp. 29905-29920
    • Hu, Y.1    Guimond, S.E.2    Travers, P.3    Cadman, S.4    Hohenester, E.5    Turnbull, J.E.6    Kim, S.H.7    Bouloux, P.M.8
  • 54
    • 2342612634 scopus 로고    scopus 로고
    • Differential functions of the C. elegans FGF receptor in axon outgrowth and maintenance of axon position
    • Bulow, H. E.; Boulin, T.; Hobert, O., Differential functions of the C. elegans FGF receptor in axon outgrowth and maintenance of axon position. Neuron 2004, 42 (3), 367-374.
    • (2004) Neuron , vol.42 , Issue.3 , pp. 367-374
    • Bulow, H.E.1    Boulin, T.2    Hobert, O.3
  • 57
    • 78149262114 scopus 로고    scopus 로고
    • Biochemical dissection of Anosmin-1 interaction with FGFR1 and components of the extracellular matrix
    • Murcia-Belmonte, V.; Esteban, P. F.; Garcia-Gonzalez, D.; De Castro, F., Biochemical dissection of Anosmin-1 interaction with FGFR1 and components of the extracellular matrix. J Neurochem 2010, 115 (5), 1256-1265.
    • (2010) J Neurochem , vol.115 , Issue.5 , pp. 1256-1265
    • Murcia-Belmonte, V.1    Esteban, P.F.2    Garcia-Gonzalez, D.3    De Castro, F.4
  • 59
    • 78650528556 scopus 로고    scopus 로고
    • Defective gonadotropin-releasing hormone neuron migration in mice lacking SEMA3A signalling through NRP1 and NRP2: Implications for the aetiology of hypogonadotropic hypogonadism
    • Cariboni, A.; Davidson, K.; Rakic, S.; Maggi, R.; Parnavelas, J. G.; Ruhrberg, C., Defective gonadotropin-releasing hormone neuron migration in mice lacking SEMA3A signalling through NRP1 and NRP2: implications for the aetiology of hypogonadotropic hypogonadism. Hum Mol Genet 2010, 20 (2), 336-344.
    • (2010) Hum Mol Genet , vol.20 , Issue.2 , pp. 336-344
    • Cariboni, A.1    Davidson, K.2    Rakic, S.3    Maggi, R.4    Parnavelas, J.G.5    Ruhrberg, C.6
  • 63
    • 18044383585 scopus 로고    scopus 로고
    • Semaphorin 3A displays a punctate distribution on the surface of neuronal cells and interacts with proteoglycans in the extracellular matrix
    • De Wit, J.; De Winter, F.; Klooster, J.; Verhaagen, J., Semaphorin 3A displays a punctate distribution on the surface of neuronal cells and interacts with proteoglycans in the extracellular matrix. Mol Cell Neurosci 2005, 29 (1), 40-55.
    • (2005) Mol Cell Neurosci , vol.29 , Issue.1 , pp. 40-55
    • De Wit, J.1    De Winter, F.2    Klooster, J.3    Verhaagen, J.4
  • 64
    • 0025211862 scopus 로고
    • Identical twins discordant for Kallmann's syndrome
    • Hipkin, L. J.; Casson, I. F.; Davis, J. C., Identical twins discordant for Kallmann's syndrome. J Med Genet 1990, 27 (3), 198-199.
    • (1990) J Med Genet , vol.27 , Issue.3 , pp. 198-199
    • Hipkin, L.J.1    Casson, I.F.2    Davis, J.C.3
  • 66
    • 0034743423 scopus 로고    scopus 로고
    • A regulatory cascade of three homeobox genes, ceh-10, ttx-3 and ceh-23, controls cell fate specification of a defined interneuron class in C. elegans
    • Altun-Gultekin, Z.; Andachi, Y.; Tsalik, E. L.; Pilgrim, D.; Kohara, Y.; Hobert, O., A regulatory cascade of three homeobox genes, ceh-10, ttx-3 and ceh-23, controls cell fate specification of a defined interneuron class in C. elegans. Development 2001, 128 (11), 1951-1969.
    • (2001) Development , vol.128 , Issue.11 , pp. 1951-1969
    • Altun-Gultekin, Z.1    Andachi, Y.2    Tsalik, E.L.3    Pilgrim, D.4    Kohara, Y.5    Hobert, O.6
  • 67
    • 0142074784 scopus 로고    scopus 로고
    • LIM homeobox gene-dependent expression of biogenic amine receptors in restricted regions of the C. elegans nervous system
    • Tsalik, E. L.; Niacaris, T.; Wenick, A. S.; Pau, K.; Avery, L.; Hobert, O., LIM homeobox gene-dependent expression of biogenic amine receptors in restricted regions of the C. elegans nervous system. Dev Biol 2003, 263 (1), 81-102.
    • (2003) Dev Biol , vol.263 , Issue.1 , pp. 81-102
    • Tsalik, E.L.1    Niacaris, T.2    Wenick, A.S.3    Pau, K.4    Avery, L.5    Hobert, O.6


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