메뉴 건너뛰기




Volumn 97, Issue 9, 2013, Pages 571-577

Plac1 (placenta-specific 1) is widely expressed during fetal development and is associated with a lethal form of hydrocephalus

Author keywords

Birth defects; Embryo; Hydrocephalus; Plac1; Placenta; X Chromosome

Indexed keywords

BETA GALACTOSIDASE; PLACENTA SPECIFIC 1 PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

EID: 84884706588     PISSN: 15420752     EISSN: 15420760     Source Type: Journal    
DOI: 10.1002/bdra.23171     Document Type: Article
Times cited : (11)

References (25)
  • 1
    • 0001387754 scopus 로고
    • Hereditary stenosis of the aqueduct of sylvius as a cause of congenital hydrocephalus
    • Bickers DS, Adams RD. 1949. Hereditary stenosis of the aqueduct of sylvius as a cause of congenital hydrocephalus. Brain 72:246-262.
    • (1949) Brain , vol.72 , pp. 246-262
    • Bickers, D.S.1    Adams, R.D.2
  • 2
    • 0026545275 scopus 로고
    • A large domain common to sperm receptors (ZP2 and ZP3) and TGF-beta type III receptor
    • Bork P, Sander C. 1992. A large domain common to sperm receptors (ZP2 and ZP3) and TGF-beta type III receptor. FEBS Lett 300:237-240.
    • (1992) FEBS Lett , vol.300 , pp. 237-240
    • Bork, P.1    Sander, C.2
  • 3
    • 0018361423 scopus 로고
    • Recurrence risk for congenital hydrocephalus
    • Burton BK. 1979. Recurrence risk for congenital hydrocephalus. Clin Genet 16:47-53.
    • (1979) Clin Genet , vol.16 , pp. 47-53
    • Burton, B.K.1
  • 4
    • 0034665428 scopus 로고    scopus 로고
    • PLAC1, an Xq26 gene with placenta-specific expression
    • Cocchia M, Huber R, Pantano S, et al. 2000. PLAC1, an Xq26 gene with placenta-specific expression. Genomics 68:305-312.
    • (2000) Genomics , vol.68 , pp. 305-312
    • Cocchia, M.1    Huber, R.2    Pantano, S.3
  • 5
    • 0031984128 scopus 로고    scopus 로고
    • Errors in corticospinal axon guidance in mice lacking the neural cell adhesion molecule L1
    • Cohen NR, Taylor JS, Scott LB, et al. 1997. Errors in corticospinal axon guidance in mice lacking the neural cell adhesion molecule L1. Curr Biol 8:26-33.
    • (1997) Curr Biol , vol.8 , pp. 26-33
    • Cohen, N.R.1    Taylor, J.S.2    Scott, L.B.3
  • 6
    • 0030666794 scopus 로고    scopus 로고
    • Disruption of the gene coding for the cell adhesion molecule L1 leads to malformations of the nervous system in mice
    • Dahme M, Bartsch U, Martini R, et al. 1997. Disruption of the gene coding for the cell adhesion molecule L1 leads to malformations of the nervous system in mice. Nat Genet 17:346-349.
    • (1997) Nat Genet , vol.17 , pp. 346-349
    • Dahme, M.1    Bartsch, U.2    Martini, R.3
  • 7
    • 0000005625 scopus 로고
    • The syndrome of sex-linked hydrocephalus
    • Edwards JH. 1961. The syndrome of sex-linked hydrocephalus. Arch Dis Child 36:486-493.
    • (1961) Arch Dis Child , vol.36 , pp. 486-493
    • Edwards, J.H.1
  • 8
    • 0343294007 scopus 로고    scopus 로고
    • Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1 disease
    • Finckh U, Schroder J, Ressler B, et al. 2000. Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1 disease. Am J Med Genet 92:40-46.
    • (2000) Am J Med Genet , vol.92 , pp. 40-46
    • Finckh, U.1    Schroder, J.2    Ressler, B.3
  • 9
    • 0022571148 scopus 로고
    • X-linked hydrocephalus: a survey of a 20 year period in Victoria, Australia
    • Halliday J, Chow CW, Wallace D, Danks DM. 1986. X-linked hydrocephalus: a survey of a 20 year period in Victoria, Australia. J Med Genet 23:23-31.
    • (1986) J Med Genet , vol.23 , pp. 23-31
    • Halliday, J.1    Chow, C.W.2    Wallace, D.3    Danks, D.M.4
  • 10
    • 0344530903 scopus 로고    scopus 로고
    • The role of the X chromosome in mammalian extra embryonic development
    • Hemberger M. 2002. The role of the X chromosome in mammalian extra embryonic development. Cytogenet Genome Res 99:210-217.
    • (2002) Cytogenet Genome Res , vol.99 , pp. 210-217
    • Hemberger, M.1
  • 11
    • 0032856381 scopus 로고    scopus 로고
    • Genetic dissection of X-linked interspecific hybrid placental dysplasia in congenic mouse strains
    • Hemberger MC, Pearsall RS, Zechner U, et al. 1999. Genetic dissection of X-linked interspecific hybrid placental dysplasia in congenic mouse strains. Genetics 153:383-390.
    • (1999) Genetics , vol.153 , pp. 383-390
    • Hemberger, M.C.1    Pearsall, R.S.2    Zechner, U.3
  • 12
    • 33749252180 scopus 로고    scopus 로고
    • Fanconi anaemia complememtation group B presenting as X linked VACTERL with hydrocephalus syndrome
    • Holden ST, Cox JJ, Kesterton I, et al. 2006. Fanconi anaemia complememtation group B presenting as X linked VACTERL with hydrocephalus syndrome. J Med Genet 43:750-754.
    • (2006) J Med Genet , vol.43 , pp. 750-754
    • Holden, S.T.1    Cox, J.J.2    Kesterton, I.3
  • 13
    • 84864825655 scopus 로고    scopus 로고
    • Plac1 (Placenta-specific 1) is essential for normal placental and embryonic development
    • Jackman S, Kong X, Fant ME. 2012. Plac1 (Placenta-specific 1) is essential for normal placental and embryonic development. Molecular Reproduction and Development, 79:564-572.
    • (2012) Molecular Reproduction and Development , vol.79 , pp. 564-572
    • Jackman, S.1    Kong, X.2    Fant, M.E.3
  • 14
    • 0027250705 scopus 로고
    • A missense mutation confirms the L1 defect in X-linked hydrocephalus (HSAS)
    • Jouet M, Rosenthal A, McFarlane J, et al. 1993. A missense mutation confirms the L1 defect in X-linked hydrocephalus (HSAS). Nat Genet 4:331.
    • (1993) Nat Genet , vol.4 , pp. 331
    • Jouet, M.1    Rosenthal, A.2    McFarlane, J.3
  • 15
    • 0036307181 scopus 로고    scopus 로고
    • The ZP domain is a conserved module for polymerization of extracellular proteins
    • Jovine L, Qi H, Williams Z, et al. 2002. The ZP domain is a conserved module for polymerization of extracellular proteins. Nat Cell Biol 2002;4:457-461.
    • (2002) Nat Cell Biol , vol.2002 , Issue.4 , pp. 457-461
    • Jovine, L.1    Qi, H.2    Williams, Z.3
  • 16
    • 1942469466 scopus 로고    scopus 로고
    • A duplicated motif controls assembly of zona pellucida domain proteins
    • Jovine L, Qi H, Williams Z, et al. 2004. A duplicated motif controls assembly of zona pellucida domain proteins. Proc Natl Acad Sci U S A 101:5922-5927.
    • (2004) Proc Natl Acad Sci U S A , vol.101 , pp. 5922-5927
    • Jovine, L.1    Qi, H.2    Williams, Z.3
  • 17
    • 0033828234 scopus 로고    scopus 로고
    • Late onset hydrocephalus with normal cerebrospinal fluid pressure
    • Katsuragi S, Teraoka K, Ikegami K, et al. 2000. Late onset hydrocephalus with normal cerebrospinal fluid pressure. Psychiatry Clin Neurosci 54:487-492.
    • (2000) Psychiatry Clin Neurosci , vol.54 , pp. 487-492
    • Katsuragi, S.1    Teraoka, K.2    Ikegami, K.3
  • 18
    • 80053125098 scopus 로고    scopus 로고
    • X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations
    • McCauly, Masand N, McGowan R, et al. 2011. X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations. Am J Med Genet A 155:2370-2380.
    • (2011) Am J Med Genet A , vol.155 , pp. 2370-2380
    • McCauly, M.N.1    McGowan, R.2
  • 19
    • 35948945357 scopus 로고    scopus 로고
    • PLAC1, a trophoblast-specific cell surface protein, is expressed in a range of human tumors and elicits spontaneous antibody responses
    • Silva WA Jr, Gnjatic S, Ritter E, et al. 2007. PLAC1, a trophoblast-specific cell surface protein, is expressed in a range of human tumors and elicits spontaneous antibody responses. Cancer Immun 7:18.
    • (2007) Cancer Immun , vol.7 , pp. 18
    • Silva Jr, W.A.1    Gnjatic, S.2    Ritter, E.3
  • 20
    • 11144354460 scopus 로고    scopus 로고
    • Different molecular mechanisms underlie placental overgrowth phenotypes by interspecies hybridation, Cloning and ESX1 mutation
    • Singh N, Fohn LE, Wahayama T et al., 2004. Different molecular mechanisms underlie placental overgrowth phenotypes by interspecies hybridation, Cloning and ESX1 mutation. Dev. Dyn. 230:149-64.
    • (2004) Dev. Dyn. , vol.230 , pp. 149-164
    • Singh, N.1    Fohn, L.E.2    Wahayama, T.3
  • 21
    • 0027080958 scopus 로고
    • An epidemiologic study of environmental and genetic factors in congenital hydrocephalus
    • Stoll C, Alembik Y, Dott B, Roth MP. 1992. An epidemiologic study of environmental and genetic factors in congenital hydrocephalus. Eur J Epidemiol 8:797-803.
    • (1992) Eur J Epidemiol , vol.8 , pp. 797-803
    • Stoll, C.1    Alembik, Y.2    Dott, B.3    Roth, M.P.4
  • 22
    • 0034949521 scopus 로고    scopus 로고
    • Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): mutations in the L1CAM gene
    • Weller S, Gartner J. 2001. Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): mutations in the L1CAM gene. Hum Mutat 18:1-12.
    • (2001) Hum Mutat , vol.18 , pp. 1-12
    • Weller, S.1    Gartner, J.2
  • 23
    • 0029864996 scopus 로고    scopus 로고
    • An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrids
    • Zechner U, Reule M, Orth A, et al. 1996. An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrids. Nat Genet 12:398-403.
    • (1996) Nat Genet , vol.12 , pp. 398-403
    • Zechner, U.1    Reule, M.2    Orth, A.3
  • 24
    • 0035577350 scopus 로고    scopus 로고
    • A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution
    • Zechner, U, Wilda M, Kehrer-Sawatzki H, et al. 2001. A high density of X-linked genes for general cognitive ability: a run-away process shaping human evolution. Trends Genet 17:697-701.
    • (2001) Trends Genet , vol.17 , pp. 697-701
    • Zechner, U.1    Wilda, M.2    Kehrer-Sawatzki, H.3
  • 25


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.