메뉴 건너뛰기




Volumn 2015, Issue , 2015, Pages

SHIELD: An integrative gene expression database for inner ear research

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; GENE EXPRESSION REGULATION; GENETIC DATABASE; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; HUMAN; INNER EAR; MECHANOTRANSDUCTION;

EID: 84943149271     PISSN: 17580463     EISSN: None     Source Type: Journal    
DOI: 10.1093/database/bav071     Document Type: Article
Times cited : (114)

References (49)
  • 1
    • 84943147833 scopus 로고    scopus 로고
    • Whole-exome sequencing and its impact in hereditary hearing loss
    • Atik, T., Bademci, G., Diaz-Horta, O. et al. (2015) Whole-exome sequencing and its impact in hereditary hearing loss. Genet. Res., 97, e4.
    • (2015) Genet. Res. , vol.97 , pp. e4
    • Atik, T.1    Bademci, G.2    Diaz-Horta, O.3
  • 2
    • 84930607351 scopus 로고    scopus 로고
    • Sharing and specificity of co-expression networks across 35 human tissues
    • Pierson, E., Consortium, G.T., Koller, D. et al. (2015) Sharing and specificity of co-expression networks across 35 human tissues. PLoS Comput. Biol., 11, e1004220.
    • (2015) PLoS Comput. Biol. , vol.11 , pp. e1004220
    • Pierson, E.1    Consortium, G.T.2    Koller, D.3
  • 3
    • 84929015296 scopus 로고    scopus 로고
    • Human genomics. The human transcriptome across tissues and individuals
    • Mele, M., Ferreira, P.G., Reverter, F. et al. (2015) Human genomics. The human transcriptome across tissues and individuals. Science, 348, 660-665.
    • (2015) Science , vol.348 , pp. 660-665
    • Mele, M.1    Ferreira, P.G.2    Reverter, F.3
  • 4
    • 79960953181 scopus 로고    scopus 로고
    • Developmental profiling of spiral ganglion neurons reveals insights into auditory circuit assembly
    • Lu, C.C., Appler, J.M., Houseman, E.A. et al. (2011) Developmental profiling of spiral ganglion neurons reveals insights into auditory circuit assembly. J. Neurosci., 31, 10903-10918.
    • (2011) J. Neurosci. , vol.31 , pp. 10903-10918
    • Lu, C.C.1    Appler, J.M.2    Houseman, E.A.3
  • 5
    • 84875890050 scopus 로고    scopus 로고
    • Molecular architecture of the chick vestibular hair bundle
    • Shin, J.B., Krey, J.F., Hassan, A. et al. (2013) Molecular architecture of the chick vestibular hair bundle. Nat. Neurosci., 16, 365-374.
    • (2013) Nat. Neurosci. , vol.16 , pp. 365-374
    • Shin, J.B.1    Krey, J.F.2    Hassan, A.3
  • 6
    • 84905851547 scopus 로고    scopus 로고
    • Characterization of transcriptomes of cochlear inner and outer hair cells
    • Liu, H., Pecka, J.L., Zhang, Q. et al. (2014) Characterization of transcriptomes of cochlear inner and outer hair cells. J. Neurosci., 34, 11085-11095.
    • (2014) J. Neurosci. , vol.34 , pp. 11085-11095
    • Liu, H.1    Pecka, J.L.2    Zhang, Q.3
  • 7
    • 34548755017 scopus 로고    scopus 로고
    • Gene expression profiling identifies Hes6 as a transcriptional target of ATOH1 in cochlear hair cells
    • Scheffer, D., Sage, C., Corey, D.P. et al. (2007) Gene expression profiling identifies Hes6 as a transcriptional target of ATOH1 in cochlear hair cells. FEBS Lett., 581, 4651-4656.
    • (2007) FEBS Lett. , vol.581 , pp. 4651-4656
    • Scheffer, D.1    Sage, C.2    Corey, D.P.3
  • 8
    • 74449084340 scopus 로고    scopus 로고
    • The alpha1 subunit of nicotinic acetylcholine receptors in the inner ear: Transcriptional regulation by ATOH1 and co-expression with the gamma subunit in hair cells
    • Scheffer, D., Sage, C., Plazas, P.V. et al. (2007) The alpha1 subunit of nicotinic acetylcholine receptors in the inner ear: transcriptional regulation by ATOH1 and co-expression with the gamma subunit in hair cells. J. Neurochem., 103, 2651-2664.
    • (2007) J. Neurochem. , vol.103 , pp. 2651-2664
    • Scheffer, D.1    Sage, C.2    Plazas, P.V.3
  • 9
    • 84929378116 scopus 로고    scopus 로고
    • Gene expression by mouse inner ear hair cells during development
    • Scheffer, D.I., Shen, J., Corey, D.P. et al. (2015) Gene expression by mouse inner ear hair cells during development. J. Neurosci., 35, 6366-6380.
    • (2015) J. Neurosci. , vol.35 , pp. 6366-6380
    • Scheffer, D.I.1    Shen, J.2    Corey, D.P.3
  • 10
    • 84920875844 scopus 로고    scopus 로고
    • C-MYC transcriptionally amplifies SOX2 target genes to regulate self-renewal in multipotent otic progenitor cells
    • Kwan, K.Y., Shen, J. and Corey, D.P. (2015) C-MYC transcriptionally amplifies SOX2 target genes to regulate self-renewal in multipotent otic progenitor cells. Stem Cell Rep., 4, 47-60.
    • (2015) Stem Cell Rep. , vol.4 , pp. 47-60
    • Kwan, K.Y.1    Shen, J.2    Corey, D.P.3
  • 12
    • 84891788593 scopus 로고    scopus 로고
    • The Mouse Genome Database: Integration of and access to knowledge about the laboratory mouse
    • Blake, J.A., Bult, C.J., Eppig, J.T. et al. (2014) The Mouse Genome Database: integration of and access to knowledge about the laboratory mouse. Nucleic Acids Res., 42, D810-D817.
    • (2014) Nucleic Acids Res. , vol.42 , pp. D810-D817
    • Blake, J.A.1    Bult, C.J.2    Eppig, J.T.3
  • 13
    • 84891771466 scopus 로고    scopus 로고
    • The UCSC Genome Browser database: 2014 update
    • Karolchik, D., Barber, G.P., Casper, J. et al. (2014) The UCSC Genome Browser database: 2014 update. Nucleic Acids Res., 42, D764-D770.
    • (2014) Nucleic Acids Res. , vol.42 , pp. D764-D770
    • Karolchik, D.1    Barber, G.P.2    Casper, J.3
  • 14
    • 84941044607 scopus 로고    scopus 로고
    • Genenames.org: The HGNC resources in 2015
    • Gray, K.A., Yates, B., Seal, R.L. et al. (2015) Genenames.org: the HGNC resources in 2015. Nucleic Acids Res., 43, D1079-D1085.
    • (2015) Nucleic Acids Res. , vol.43 , pp. D1079-D1085
    • Gray, K.A.1    Yates, B.2    Seal, R.L.3
  • 16
    • 84946069451 scopus 로고    scopus 로고
    • UniProt: A hub for protein information
    • UniProt, C. (2015) UniProt: a hub for protein information. Nucleic Acids Res., 43, D204-D212.
    • (2015) Nucleic Acids Res. , vol.43 , pp. D204-D212
    • UniProt, C.1
  • 17
    • 0035910270 scopus 로고    scopus 로고
    • Predicting transmembrane protein topology with a hidden Markov model: Application to complete genomes
    • Krogh, A., Larsson, B., von Heijne, G. et al. (2001) Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J. Mol. Biol., 305, 567-580.
    • (2001) J. Mol. Biol. , vol.305 , pp. 567-580
    • Krogh, A.1    Larsson, B.2    Von Heijne, G.3
  • 18
    • 0033816925 scopus 로고    scopus 로고
    • A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
    • Verpy, E., Leibovici, M., Zwaenepoel, I. et al. (2000) A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nat. Genet., 26, 51-55.
    • (2000) Nat. Genet. , vol.26 , pp. 51-55
    • Verpy, E.1    Leibovici, M.2    Zwaenepoel, I.3
  • 19
    • 84868207944 scopus 로고    scopus 로고
    • Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48
    • Riazuddin, S., Belyantseva, I.A., Giese, A.P. et al. (2012) Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48. Nat. Genet., 44, 1265-1271.
    • (2012) Nat. Genet. , vol.44 , pp. 1265-1271
    • Riazuddin, S.1    Belyantseva, I.A.2    Giese, A.P.3
  • 20
    • 0036510053 scopus 로고    scopus 로고
    • Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function
    • Kurima, K., Peters, L.M., Yang, Y. et al. (2002) Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nat. Genet., 30, 277-284.
    • (2002) Nat. Genet. , vol.30 , pp. 277-284
    • Kurima, K.1    Peters, L.M.2    Yang, Y.3
  • 21
    • 0030960855 scopus 로고    scopus 로고
    • Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
    • Liu, X.Z., Walsh, J., Mburu, P. et al. (1997) Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nat. Genet., 16, 188-190.
    • (1997) Nat. Genet. , vol.16 , pp. 188-190
    • Liu, X.Z.1    Walsh, J.2    Mburu, P.3
  • 22
    • 0030951102 scopus 로고    scopus 로고
    • The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
    • Weil, D., Kussel, P., Blanchard, S. et al. (1997) The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. Nat. Genet., 16, 191-193.
    • (1997) Nat. Genet. , vol.16 , pp. 191-193
    • Weil, D.1    Kussel, P.2    Blanchard, S.3
  • 23
    • 0033546004 scopus 로고    scopus 로고
    • Math1: An essential gene for the generation of inner ear hair cells
    • Bermingham, N.A., Hassan, B.A., Price, S.D. et al. (1999) Math1: an essential gene for the generation of inner ear hair cells. Science, 284, 1837-1841.
    • (1999) Science , vol.284 , pp. 1837-1841
    • Bermingham, N.A.1    Hassan, B.A.2    Price, S.D.3
  • 24
    • 17844388072 scopus 로고    scopus 로고
    • Sox2 is required for sensory organ development in the mammalian inner ear
    • Kiernan, A.E., Pelling, A.L., Leung, K.K. et al. (2005) Sox2 is required for sensory organ development in the mammalian inner ear. Nature, 434, 1031-1035.
    • (2005) Nature , vol.434 , pp. 1031-1035
    • Kiernan, A.E.1    Pelling, A.L.2    Leung, K.K.3
  • 25
    • 84922355311 scopus 로고    scopus 로고
    • A short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing function
    • Francis, S.P., Krey, J.F., Krystofiak, E.S. et al. (2015) A short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing function. J. Neurosci., 35, 1999-2014.
    • (2015) J. Neurosci. , vol.35 , pp. 1999-2014
    • Francis, S.P.1    Krey, J.F.2    Krystofiak, E.S.3
  • 26
    • 84925674615 scopus 로고    scopus 로고
    • XIRP2, an actinbinding protein essential for inner ear hair-cell stereocilia
    • Scheffer, D.I., Zhang, D.S., Shen, J. et al. (2015) XIRP2, an actinbinding protein essential for inner ear hair-cell stereocilia. Cell Rep., 10, 1811-1818.
    • (2015) Cell Rep. , vol.10 , pp. 1811-1818
    • Scheffer, D.I.1    Zhang, D.S.2    Shen, J.3
  • 27
    • 0033852532 scopus 로고    scopus 로고
    • Misexpression of basic helix-loop-helix genes in the murine cerebral cortex affects cell fate choices and neuronal survival
    • Cai, L., Morrow, E.M. and Cepko, C.L. (2000) Misexpression of basic helix-loop-helix genes in the murine cerebral cortex affects cell fate choices and neuronal survival. Development, 127, 3021-3030.
    • (2000) Development , vol.127 , pp. 3021-3030
    • Cai, L.1    Morrow, E.M.2    Cepko, C.L.3
  • 28
    • 79956291837 scopus 로고    scopus 로고
    • NeuroD factors regulate cell fate and neurite stratification in the developing retina
    • Cherry, T.J., Wang, S., Bormuth, I. et al. (2011) NeuroD factors regulate cell fate and neurite stratification in the developing retina. J. Neurosci., 31, 7365-7379.
    • (2011) J. Neurosci. , vol.31 , pp. 7365-7379
    • Cherry, T.J.1    Wang, S.2    Bormuth, I.3
  • 29
    • 79960843532 scopus 로고    scopus 로고
    • Neurod6 expression defines new retinal amacrine cell subtypes and regulates their fate
    • Kay, J.N., Voinescu, P.E., Chu, M.W. et al. (2011) Neurod6 expression defines new retinal amacrine cell subtypes and regulates their fate. Nat. Neurosci., 14, 965-972.
    • (2011) Nat. Neurosci. , vol.14 , pp. 965-972
    • Kay, J.N.1    Voinescu, P.E.2    Chu, M.W.3
  • 30
    • 40349112978 scopus 로고    scopus 로고
    • Barhl1 regulatory sequences required for cell-specific gene expression and autoregulation in the inner ear and central nervous system
    • Chellappa, R., Li, S., Pauley, S. et al. (2008) Barhl1 regulatory sequences required for cell-specific gene expression and autoregulation in the inner ear and central nervous system. Mol. Cell. Biol., 28, 1905-1914.
    • (2008) Mol. Cell. Biol. , vol.28 , pp. 1905-1914
    • Chellappa, R.1    Li, S.2    Pauley, S.3
  • 31
    • 0026760488 scopus 로고
    • A comparative structural characterization of the human NSCL-1 and NSCL-2 genes. Two basic helix-loop-helix genes expressed in the developing nervous system
    • Lipkowitz, S., Gobel, V., Varterasian, M.L. et al. (1992) A comparative structural characterization of the human NSCL-1 and NSCL-2 genes. Two basic helix-loop-helix genes expressed in the developing nervous system. J. Biol. Chem., 267, 21065-21071.
    • (1992) J. Biol. Chem. , vol.267 , pp. 21065-21071
    • Lipkowitz, S.1    Gobel, V.2    Varterasian, M.L.3
  • 32
    • 0031762950 scopus 로고    scopus 로고
    • GeneCards: A novel functional genomics compendium with automated data mining and query reformulation support
    • Rebhan, M., Chalifa-Caspi, V., Prilusky, J. et al. (1998) GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support. Bioinformatics, 14, 656-664.
    • (1998) Bioinformatics , vol.14 , pp. 656-664
    • Rebhan, M.1    Chalifa-Caspi, V.2    Prilusky, J.3
  • 33
    • 84873329892 scopus 로고    scopus 로고
    • The LINC complex is essential for hearing
    • Horn, H.F., Brownstein, Z., Lenz, D.R. et al. (2013) The LINC complex is essential for hearing. J. Clin. Invest., 123, 740-750.
    • (2013) J. Clin. Invest. , vol.123 , pp. 740-750
    • Horn, H.F.1    Brownstein, Z.2    Lenz, D.R.3
  • 34
    • 84877620653 scopus 로고    scopus 로고
    • Estrogen-related receptor gamma and hearing function: Evidence of a role in humans and mice
    • Nolan, L.S., Maier, H., Hermans-Borgmeyer, I. et al. (2013)Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice. Neurobiol. Aging, 34, 2077 e2071-e2079.
    • (2013) Neurobiol. Aging , vol.34 , Issue.2077 , pp. e2071-e2079
    • Nolan, L.S.1    Maier, H.2    Hermans-Borgmeyer, I.3
  • 35
    • 84898803026 scopus 로고    scopus 로고
    • A frameshift mutation in GRXCR2 causes recessively inherited hearing loss
    • Imtiaz, A., Kohrman, D.C. and Naz, S. (2014) A frameshift mutation in GRXCR2 causes recessively inherited hearing loss. Hum. Mutat., 35, 618-624.
    • (2014) Hum. Mutat. , vol.35 , pp. 618-624
    • Imtiaz, A.1    Kohrman, D.C.2    Naz, S.3
  • 36
    • 84867953576 scopus 로고    scopus 로고
    • USH1K, a novel locus for type i Usher syndrome, maps to chromosome 10p11.21-q21.1
    • Jaworek, T.J., Bhatti, R., Latief, N. et al. (2012) USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1. J. Hum. Genet., 57, 633-637.
    • (2012) J. Hum. Genet. , vol.57 , pp. 633-637
    • Jaworek, T.J.1    Bhatti, R.2    Latief, N.3
  • 37
    • 84863318507 scopus 로고    scopus 로고
    • The function and molecular identity of inward rectifier channels in vestibular hair cells of the mouse inner ear
    • Levin, M.E. and Holt, J.R. (2012) The function and molecular identity of inward rectifier channels in vestibular hair cells of the mouse inner ear. J. Neurophysiol., 108, 175-186.
    • (2012) J. Neurophysiol. , vol.108 , pp. 175-186
    • Levin, M.E.1    Holt, J.R.2
  • 38
    • 84869053060 scopus 로고    scopus 로고
    • Elongation factor 1 alpha1 and genes associated with Usher syndromes are downstream targets of GBX2
    • Roeseler, D.A., Sachdev, S., Buckley, D.M. et al. (2012) Elongation factor 1 alpha1 and genes associated with Usher syndromes are downstream targets of GBX2. PloS One, 7, e47366.
    • (2012) PloS One , vol.7 , pp. e47366
    • Roeseler, D.A.1    Sachdev, S.2    Buckley, D.M.3
  • 39
    • 84880262810 scopus 로고    scopus 로고
    • The genetics of hair cell development and regeneration
    • Groves, A.K., Zhang, K.D. and Fekete, D.M. (2013) The genetics of hair cell development and regeneration. Annu. Rev. Neurosci., 36, 361-381.
    • (2013) Annu. Rev. Neurosci. , vol.36 , pp. 361-381
    • Groves, A.K.1    Zhang, K.D.2    Fekete, D.M.3
  • 40
    • 84884696370 scopus 로고    scopus 로고
    • An alteration in ELMOD3, an Arl2 GTPase-activating protein, is associated with hearing impairment in humans
    • Jaworek, T.J., Richard, E.M., Ivanova, A.A. et al. (2013) An alteration in ELMOD3, an Arl2 GTPase-activating protein, is associated with hearing impairment in humans. PLoS Genet., 9, e1003774.
    • (2013) PLoS Genet. , vol.9 , pp. e1003774
    • Jaworek, T.J.1    Richard, E.M.2    Ivanova, A.A.3
  • 41
    • 84875212043 scopus 로고    scopus 로고
    • Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness
    • Lentz, J.J., Jodelka, F.M., Hinrich, A.J. et al. (2013) Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness. Nat. Med., 19, 345-350.
    • (2013) Nat. Med. , vol.19 , pp. 345-350
    • Lentz, J.J.1    Jodelka, F.M.2    Hinrich, A.J.3
  • 42
    • 84874127342 scopus 로고    scopus 로고
    • Diaphanous homolog 3 (Diap3) overexpression causes progressive hearing loss and inner hair cell defects in a transgenic mouse model of human deafness
    • Schoen, C.J., Burmeister, M. and Lesperance, M.M. (2013) Diaphanous homolog 3 (Diap3) overexpression causes progressive hearing loss and inner hair cell defects in a transgenic mouse model of human deafness. PloS One, 8, e56520.
    • (2013) PloS One , vol.8 , pp. e56520
    • Schoen, C.J.1    Burmeister, M.2    Lesperance, M.M.3
  • 43
    • 84880639106 scopus 로고    scopus 로고
    • Slit/Robo signaling mediates spatial positioning of spiral ganglion neurons during development of cochlear innervation
    • Wang, S.Z., Ibrahim, L.A., Kim, Y.J. et al. (2013) Slit/Robo signaling mediates spatial positioning of spiral ganglion neurons during development of cochlear innervation. J. Neurosci., 33, 12242-12254.
    • (2013) J. Neurosci. , vol.33 , pp. 12242-12254
    • Wang, S.Z.1    Ibrahim, L.A.2    Kim, Y.J.3
  • 44
    • 84901983388 scopus 로고    scopus 로고
    • TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss
    • Azaiez, H., Booth, K.T., Bu, F. et al. (2014) TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. Hum. Mutat., 35, 819-823.
    • (2014) Hum. Mutat. , vol.35 , pp. 819-823
    • Azaiez, H.1    Booth, K.T.2    Bu, F.3
  • 45
    • 84897433140 scopus 로고    scopus 로고
    • Expression and replication studies to identify new candidate genes involved in normal hearing function
    • Girotto, G., Vuckovic, D., Buniello, A. et al. (2014) Expression and replication studies to identify new candidate genes involved in normal hearing function. PloS One, 9, e85352.
    • (2014) PloS One , vol.9 , pp. e85352
    • Girotto, G.1    Vuckovic, D.2    Buniello, A.3
  • 46
    • 84902300114 scopus 로고    scopus 로고
    • Nextgeneration sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways
    • Rudnicki, A., Isakov, O., Ushakov, K. et al. (2014) Nextgeneration sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways. BMC Genomics, 15, 484.
    • (2014) BMC Genomics , vol.15 , pp. 484
    • Rudnicki, A.1    Isakov, O.2    Ushakov, K.3
  • 47
    • 84901316993 scopus 로고    scopus 로고
    • Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish
    • Santos-Cortez, R.L., Lee, K., Giese, A.P. et al. (2014) Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish. Hum. Mol. Genet., 23, 3289-3298.
    • (2014) Hum. Mol. Genet. , vol.23 , pp. 3289-3298
    • Santos-Cortez, R.L.1    Lee, K.2    Giese, A.P.3
  • 48
    • 84929378157 scopus 로고    scopus 로고
    • Characterization of the transcriptome of nascent hair cells and identification of direct targets of the atoh1 transcription factor
    • Cai, T., Jen, H.I., Kang, H. et al. (2015) Characterization of the transcriptome of nascent hair cells and identification of direct targets of the atoh1 transcription factor. J.Neurosci., 35, 5870-5883.
    • (2015) J.Neurosci. , vol.35 , pp. 5870-5883
    • Cai, T.1    Jen, H.I.2    Kang, H.3
  • 49
    • 84926317037 scopus 로고    scopus 로고
    • Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome
    • Simon, M., Richard, E.M., Wang, X. et al. (2015) Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. PLoS Genet., 11, e1005097.
    • (2015) PLoS Genet. , vol.11 , pp. e1005097
    • Simon, M.1    Richard, E.M.2    Wang, X.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.