메뉴 건너뛰기




Volumn 19, Issue 1, 2003, Pages 11-18

Characteristics of hydrocephalus expression in the LEW/Jms rat strain with inherited disease

Author keywords

Backcross; Breeding; Fisher F344; Hydrocephalus severity; Recessive; Sex linkage

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BRAIN VENTRICLE DILATATION; BREEDING LINE; CONTROLLED STUDY; CROSS BREEDING; DISEASE SEVERITY; FEMALE; FREQUENCY ANALYSIS; HYDROCEPHALUS; LETHALITY; MALE; NONHUMAN; PRIORITY JOURNAL; RAT; RAT STRAIN; SEX CHROMOSOMAL INHERITANCE; SEX DIFFERENCE; SEX LINKAGE; ANIMAL; BRAIN; BREEDING; COMPARATIVE STUDY; FISCHER 344 RAT; GENETICS; GROWTH, DEVELOPMENT AND AGING; HOSPITALIZATION; LEWIS RAT; NEWBORN; PATHOLOGY;

EID: 0037984456     PISSN: 02567040     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00381-002-0671-3     Document Type: Article
Times cited : (8)

References (51)
  • 1
    • 0027538372 scopus 로고
    • Autosomal recessive congenital stenosis of aqueduct of Sylvius
    • Barros-Nunes P, Rivas F (1993) Autosomal recessive congenital stenosis of aqueduct of Sylvius. Genet Couns 4:19-23
    • (1993) Genet. Couns. , vol.4 , pp. 19-23
    • Barros-Nunes, P.1    Rivas, F.2
  • 2
    • 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
  • 3
    • 0015272936 scopus 로고
    • New mutant mouse with communicating hydrocephalus and secondary aqueduct stenosis
    • Borit A, Sidman RL (1972) New mutant mouse with communicating hydrocephalus and secondary aqueduct stenosis. Acta Neuropathol (Berl) 21:316-331
    • (1972) Acta Neuropathol. (Berl) , vol.21 , pp. 316-331
    • Borit, A.1    Sidman, R.L.2
  • 6
    • 0018361423 scopus 로고
    • Recurrence risks for congenital hydrocephalus
    • Burton BK (1979) Recurrence risks for congenital hydrocephalus. Clin Genet 16:47-53
    • (1979) Clin. Genet. , vol.16 , pp. 47-53
    • Burton, B.K.1
  • 8
    • 0032530312 scopus 로고    scopus 로고
    • Mutation of the mouse hepatocyte nuclear factor/forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry
    • Chen J, Knowles HJ, Hebert JL, Hackett BP (1998) Mutation of the mouse hepatocyte nuclear factor/ forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry. J Clin Invest 102:1077-1082
    • (1998) J. Clin. Invest. , vol.102 , pp. 1077-1082
    • Chen, J.1    Knowles, H.J.2    Hebert, J.L.3    Hackett, B.P.4
  • 12
    • 0033763635 scopus 로고    scopus 로고
    • Impaired brain development and hydrocephalus in a line of transgenic mice with liver-specific expression of human insulin-like growth factor binding protein-1
    • Doublier S, Duyckaerts C, Seurin D, Binoux M (2000) Impaired brain development and hydrocephalus in a line of transgenic mice with liver-specific expression of human insulin-like growth factor binding protein-1. Growth Horm IGF Res 10:267-274
    • (2000) Growth Horm. IGF Res. , vol.10 , pp. 267-274
    • Doublier, S.1    Duyckaerts, C.2    Seurin, D.3    Binoux, M.4
  • 13
    • 0028989549 scopus 로고
    • Overexpression of TGF-beta 1 in the central nervous system of transgenic mice results in hydrocephalus
    • Galbreath E, Kim SJ, Park K, Brenner M, Messing A (1995) Overexpression of TGF-beta 1 in the central nervous system of transgenic mice results in hydrocephalus. J Neuropathol Exp Neurol 54:339-349
    • (1995) J. Neuropathol. Exp. Neurol. , vol.54 , pp. 339-349
    • Galbreath, E.1    Kim, S.J.2    Park, K.3    Brenner, M.4    Messing, A.5
  • 14
    • 0003290037 scopus 로고
    • Congenital hydrocephalus in the mouse, a case of spurious pleiotropism
    • Gruneberg H (1943) Congenital hydrocephalus in the mouse, a case of spurious pleiotropism. J Genet 45:1-21
    • (1943) J. Genet. , vol.45 , pp. 1-21
    • Gruneberg, H.1
  • 15
    • 0002700029 scopus 로고
    • Two new mutant genes in the house mouse
    • Gruneberg H (1943) Two new mutant genes in the house mouse. J Genet 45:22-28
    • (1943) J. Genet. , vol.45 , pp. 22-28
    • Gruneberg, H.1
  • 16
    • 0032730617 scopus 로고    scopus 로고
    • Autosomal recessive hydrocephalus due to congenital stenosis of the aqueduct of Sylvius
    • Hamada H, Watanabe H, Sugimoto M, Yasuoka M, Yamada N, Kubo T (1999) Autosomal recessive hydrocephalus due to congenital stenosis of the aqueduct of Sylvius. Prenat Diagn 19:1067-1069
    • (1999) Prenat. Diagn. , vol.19 , pp. 1067-1069
    • Hamada, H.1    Watanabe, H.2    Sugimoto, M.3    Yasuoka, M.4    Yamada, N.5    Kubo, T.6
  • 17
    • 0034535347 scopus 로고    scopus 로고
    • Chronologic changes of cerebral ventricular size in a transgenic model of hydrocephalus
    • Hayashi N, Leifer DW, Cohen AR (2000) Chronologic changes of cerebral ventricular size in a transgenic model of hydrocephalus. Pediatr Neurosurg 33:182-187
    • (2000) Pediatr. Neurosurg. , vol.33 , pp. 182-187
    • Hayashi, N.1    Leifer, D.W.2    Cohen, A.R.3
  • 18
    • 0028961719 scopus 로고
    • Exencephaly and hydrocephaly in mice with targeted modification of the apolipoprotein B (Apob) gene
    • Homanics GE, Maeda N, Traber MG, Dehardt DB, Sulik KK (1995) Exencephaly and hydrocephaly in mice with targeted modification of the apolipoprotein B (Apob) gene. Teratology 51:1-10
    • (1995) Teratology , vol.51 , pp. 1-10
    • Homanics, G.E.1    Maeda, N.2    Traber, M.G.3    Dehardt, D.B.4    Sulik, K.K.5
  • 19
    • 0033041178 scopus 로고    scopus 로고
    • Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcription factor gene
    • Hong HK, Lass JH, Chakravarti A (1999) Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcription factor gene. Hum Mol Genet 8:625-637
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 625-637
    • Hong, H.K.1    Lass, J.H.2    Chakravarti, A.3
  • 20
    • 0034946545 scopus 로고    scopus 로고
    • Genetic advances in central nervous system malformations in the fetus and neonate
    • Jeng LB, Tarvin R, Robin NH (2001) Genetic advances in central nervous system malformations in the fetus and neonate. Semin Pediatr Neurol 8:89-99
    • (2001) Semin. Pediatr. Neurol. , vol.8 , pp. 89-99
    • Jeng, L.B.1    Tarvin, R.2    Robin, N.H.3
  • 21
    • 0023783041 scopus 로고
    • Inherited prenatal hydrocephalus in the H-Tx rat: A morphological study
    • Jones HC, Bucknall RM (1988) Inherited prenatal hydrocephalus in the H-Tx rat: a morphological study. Neuropathol Appl Neurobiol 14:263-274
    • (1988) Neuropathol. Appl. Neurobiol. , vol.14 , pp. 263-274
    • Jones, H.C.1    Bucknall, R.M.2
  • 22
    • 0023113381 scopus 로고
    • Morphological aspects of the development of hydrocephalus in a mouse mutant (SUMS/NP)
    • Jones HC, Dack S, Ellis C (1987) Morphological aspects of the development of hydrocephalus in a mouse mutant (SUMS/NP). Acta Neuropathol (Berl) 72:268-276
    • (1987) Acta Neuropathol. (Berl) , vol.72 , pp. 268-276
    • Jones, H.C.1    Dack, S.2    Ellis, C.3
  • 24
    • 0034885661 scopus 로고    scopus 로고
    • Chromosomal linkage associated with disease severity in the hydrocephalic H-Tx rat
    • Jones HC, Carter BJ, Depelteau JS, Roman M, Morel L (2001) Chromosomal linkage associated with disease severity in the hydrocephalic H-Tx rat. Behav Genet 31: 101-111
    • (2001) Behav. Genet. , vol.31 , pp. 101-111
    • Jones, H.C.1    Carter, B.J.2    Depelteau, J.S.3    Roman, M.4    Morel, L.5
  • 26
    • 0036311618 scopus 로고    scopus 로고
    • The frequency of inherited hydrocephalus is influenced by intrauterine factors in H-Tx rats
    • Jones HC, Depelteau JS, Carter BJ, Somera KC (2002) The frequency of inherited hydrocephalus is influenced by intrauterine factors in H-Tx rats. Exp Neurol 176:213-220
    • (2002) Exp. Neurol. , vol.176 , pp. 213-220
    • Jones, H.C.1    Depelteau, J.S.2    Carter, B.J.3    Somera, K.C.4
  • 28
    • 0032511231 scopus 로고    scopus 로고
    • The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus
    • Kume T, Deng K-Y, Winfrey V, Gould DB, Walter MA, Hogan BLM (1998) The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus. Cell 93:985-996
    • (1998) Cell , vol.93 , pp. 985-996
    • Kume, T.1    Deng, K.-Y.2    Winfrey, V.3    Gould, D.B.4    Walter, M.A.5    Hogan, B.L.M.6
  • 29
    • 0032213969 scopus 로고    scopus 로고
    • Neuronal patterning by BMPs: A requirement for GDF7 in the generation of a discrete class of commissural interneurons in the mouse spinal cord
    • Lee KJ, Mendelsohn M, Jessell TM (1998) Neuronal patterning by BMPs: a requirement for GDF7 in the generation of a discrete class of commissural interneurons in the mouse spinal cord. Genes Dev 12:3394-3407
    • (1998) Genes Dev. , vol.12 , pp. 3394-3407
    • Lee, K.J.1    Mendelsohn, M.2    Jessell, T.M.3
  • 31
    • 0021161590 scopus 로고
    • The family history of uncomplicated congenital hydrocephalus: An epidemiological study based on 270 probands
    • Lorber J (1984) The family history of uncomplicated congenital hydrocephalus: an epidemiological study based on 270 probands. BMJ 289:281-284
    • (1984) BMJ , vol.289 , pp. 281-284
    • Lorber, J.1
  • 32
    • 0033784874 scopus 로고    scopus 로고
    • Ectopic engrailed 1 expression in the dorsal midline causes cell death, abnormal differentiation of circumventricular organs and errors in axonal pathfinding
    • Louvi A, Wassef M (2000) Ectopic engrailed 1 expression in the dorsal midline causes cell death, abnormal differentiation of circumventricular organs and errors in axonal pathfinding. Development 127:4061-4071
    • (2000) Development , vol.127 , pp. 4061-4071
    • Louvi, A.1    Wassef, M.2
  • 33
    • 0031266452 scopus 로고    scopus 로고
    • Hydrocephalus in the Otx2+/-mutant mouse
    • Makiyama Y, Shoji S, Mizusawa H (1997) Hydrocephalus in the Otx2+/-mutant mouse. Exp Neurol 148:215-221
    • (1997) Exp. Neurol. , vol.148 , pp. 215-221
    • Makiyama, Y.1    Shoji, S.2    Mizusawa, H.3
  • 34
    • 0035425336 scopus 로고    scopus 로고
    • Administration of FGF-2 to embryonic mouse brain induces hydrocephalic brain morphology and aberrant differentiation of neurons in the postnatal cerebral cortex
    • Ohmiya M, Fukumitsu H, Nitta A, Nomoto H, Furukawa Y, Furukawa S (2001) Administration of FGF-2 to embryonic mouse brain induces hydrocephalic brain morphology and aberrant differentiation of neurons in the postnatal cerebral cortex. J Neurosci Res 65:228-235
    • (2001) J. Neurosci. Res. , vol.65 , pp. 228-235
    • Ohmiya, M.1    Fukumitsu, H.2    Nitta, A.3    Nomoto, H.4    Furukawa, Y.5    Furukawa, S.6
  • 35
    • 0029977739 scopus 로고    scopus 로고
    • Experimental models of congenital hydrocephalus and comparable clinical problems in the fetal and neonatal periods
    • Oi S, Yamada H, Sato O, Matsumoto S (1996) Experimental models of congenital hydrocephalus and comparable clinical problems in the fetal and neonatal periods. Childs Nerv Syst 12:292-302
    • (1996) Childs Nerv. Syst. , vol.12 , pp. 292-302
    • Oi, S.1    Yamada, H.2    Sato, O.3    Matsumoto, S.4
  • 39
    • 0035830730 scopus 로고    scopus 로고
    • Severe hydrocephalus in L1-deficient mice
    • Rolf B, Kutsche M, Bartsch U (2001) Severe hydrocephalus in L1-deficient mice. Brain Res 891:247-252
    • (2001) Brain Res. , vol.891 , pp. 247-252
    • Rolf, B.1    Kutsche, M.2    Bartsch, U.3
  • 41
    • 0031957134 scopus 로고    scopus 로고
    • Congenital hydrocephalus: Nosology and guidelines for clinical approach and genetic counseling
    • Schrander-Stumpel C, Fryns J-P (1998) Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counseling. Eur J Pediatr 157:355-362
    • (1998) Eur. J. Pediatr. , vol.157 , pp. 355-362
    • Schrander-Stumpel, C.1    Fryns, J.-P.2
  • 42
    • 0023255942 scopus 로고
    • Absence of subcommissural organ in the cerebral aqueduct of congenital hydrocephalus spontaneously occurring in MT/HOK1 dr mice
    • Takeuchi IK, Kimura R, Matsuda M, Shoji R (1987) Absence of subcommissural organ in the cerebral aqueduct of congenital hydrocephalus spontaneously occurring in MT/HOK1 dr mice. Acta Neuropathol (Berl) 73:320-322
    • (1987) Acta Neuropathol. (Berl) , vol.73 , pp. 320-322
    • Takeuchi, I.K.1    Kimura, R.2    Matsuda, M.3    Shoji, R.4
  • 43
    • 0023880048 scopus 로고
    • Dysplasia of subcommissural organ in congenital hydrocephalus spontaneously occurring in CWS/Idr rats
    • Takeuchi IK, Kimura R, Shoji R (1988) Dysplasia of subcommissural organ in congenital hydrocephalus spontaneously occurring in CWS/Idr rats. Experientia 44:338-340
    • (1988) Experientia , vol.44 , pp. 338-340
    • Takeuchi, I.K.1    Kimura, R.2    Shoji, R.3
  • 44
    • 0024100092 scopus 로고
    • Autosomal recessive nonsyndromal hydrocephalus
    • (letter)
    • Teebi AS, Naguib KK (1988) Autosomal recessive nonsyndromal hydrocephalus (letter). Am J Med Genet 31:467-470
    • (1988) Am. J. Med. Genet. , vol.31 , pp. 467-470
    • Teebi, A.S.1    Naguib, K.K.2
  • 46
    • 0023866948 scopus 로고
    • Heterogeneity and recurrence risk for congenital hydrocephalus (ventriculomegaly): A prospective study
    • Varadi V, Toth Z, Torok O, Papp Z (1988) Heterogeneity and recurrence risk for congenital hydrocephalus (ventriculomegaly): a prospective study. Am J Med Genet 29:305-310
    • (1988) Am. J. Med. Genet. , vol.29 , pp. 305-310
    • Varadi, V.1    Toth, Z.2    Torok, O.3    Papp, Z.4
  • 47
    • 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
  • 48
    • 0029077755 scopus 로고
    • Increased central nervous system production of extracellular matrix components and development of hydrocephalus in transgenic mice overexpressing transforming growth factor-beta 1
    • Wyss Coray T, Feng L, Masliah E, Ruppe MD, Lee HS, Toggas SM, Rockenstein EM, Mucke L (1995) Increased central nervous system production of extracellular matrix components and development of hydrocephalus in transgenic mice overexpressing transforming growth factor-beta 1. Am J Pathol 147:53-67
    • (1995) Am. J. Pathol. , vol.147 , pp. 53-67
    • Wyss Coray, T.1    Feng, L.2    Masliah, E.3    Ruppe, M.D.4    Lee, H.S.5    Toggas, S.M.6    Rockenstein, E.M.7    Mucke, L.8
  • 49
    • 0025745506 scopus 로고
    • Prenatal aqueduct stenosis as a cause of congenital hydrocephalus in the inbred rat LEW/Jms
    • Yamada H, Oi S, Tamaki N, Masumoto S, Sudo K (1991) Prenatal aqueduct stenosis as a cause of congenital hydrocephalus in the inbred rat LEW/Jms. Childs Nerv Syst 7:218-222
    • (1991) Childs Nerv. Syst. , vol.7 , pp. 218-222
    • Yamada, H.1    Oi, S.2    Tamaki, N.3    Masumoto, S.4    Sudo, K.5
  • 50
    • 0026448299 scopus 로고
    • Histological changes in the midbrain around the aqueduct in congenital hydrocephalic rat LEW/Jms
    • Yamada H, Oi S, Tamaki N, Matsumoto S, Sudo K (1992) Histological changes in the midbrain around the aqueduct in congenital hydrocephalic rat LEW/Jms. Childs Nerv Syst 8:394-398
    • (1992) Childs Nerv. Syst. , vol.8 , pp. 394-398
    • Yamada, H.1    Oi, S.2    Tamaki, N.3    Matsumoto, S.4    Sudo, K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.