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Volumn 37, Issue 5, 2005, Pages 312-315

Idiopathic achalasia is not allelic to alacrima achalasia adrenal insufficiency syndrome at the ALADIN locus

Author keywords

AAAS gene mutations; Achalasia; Allgrove syndrome; Enteric neuropathy

Indexed keywords

GENOMIC DNA; NUCLEOTIDE; POLYPEPTIDE; AAAS PROTEIN, HUMAN; NUCLEOPORIN; PROTEIN;

EID: 24044438567     PISSN: 15908658     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dld.2004.11.006     Document Type: Article
Times cited : (19)

References (18)
  • 2
    • 0000326948 scopus 로고    scopus 로고
    • Motor physiology and motor disorders of the esophagus
    • Feldman M., Sleisenger M.H., and Scharschmidt B.F. (Eds), WB Saunders, Philadelphia
    • Clouse R.E., and Diamant N.E. Motor physiology and motor disorders of the esophagus. In: Feldman M., Sleisenger M.H., and Scharschmidt B.F. (Eds). Gastrointestinal and liver disease (1998), WB Saunders, Philadelphia 467-497
    • (1998) Gastrointestinal and liver disease , pp. 467-497
    • Clouse, R.E.1    Diamant, N.E.2
  • 5
    • 0027401367 scopus 로고
    • Varicella-zoster virus DNA in the oesophageal myenteric plexus in achalasia
    • Robertson C.S., Martin B.A., and Atkinson M. Varicella-zoster virus DNA in the oesophageal myenteric plexus in achalasia. Gut 34 (1993) 299-302
    • (1993) Gut , vol.34 , pp. 299-302
    • Robertson, C.S.1    Martin, B.A.2    Atkinson, M.3
  • 6
    • 0038639068 scopus 로고    scopus 로고
    • Antineuronal antibodies in idiopathic achalasia and gastroesophageal reflux disease
    • Moses P.L., Ellis L.M., Anees M.R., Ho W., Rothstein R.I., Meddings J.B., et al. Antineuronal antibodies in idiopathic achalasia and gastroesophageal reflux disease. Gut 52 (2003) 629-636
    • (2003) Gut , vol.52 , pp. 629-636
    • Moses, P.L.1    Ellis, L.M.2    Anees, M.R.3    Ho, W.4    Rothstein, R.I.5    Meddings, J.B.6
  • 8
    • 0026019711 scopus 로고
    • Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima
    • Moore P.S., Couch R.M., Perry Y.S., Shuckett E.P., and Winter J.S. Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima. Clin Endocrinol 34 (1991) 107-114
    • (1991) Clin Endocrinol , vol.34 , pp. 107-114
    • Moore, P.S.1    Couch, R.M.2    Perry, Y.S.3    Shuckett, E.P.4    Winter, J.S.5
  • 10
    • 0032442427 scopus 로고    scopus 로고
    • Achalasia: a critical review of epidemiological studies
    • Podas T., Eaden J., Mayberry M., and Mayberry J. Achalasia: a critical review of epidemiological studies. Am J Gastroenterol 93 (1998) 2345-2347
    • (1998) Am J Gastroenterol , vol.93 , pp. 2345-2347
    • Podas, T.1    Eaden, J.2    Mayberry, M.3    Mayberry, J.4
  • 11
    • 17944382121 scopus 로고    scopus 로고
    • Spectrum of mutations of the AAAS gene in Allgrove Syndrome: lack of mutations in six kindreds with isolated resistance to corticotropin
    • Sandrini F., Farmakidis C., Kirschner L.S., Wu S.M., Tullio-Pelet A., Lyonnet S., et al. Spectrum of mutations of the AAAS gene in Allgrove Syndrome: lack of mutations in six kindreds with isolated resistance to corticotropin. J Clin Endocrinol Metab 86 (2001) 5433-5437
    • (2001) J Clin Endocrinol Metab , vol.86 , pp. 5433-5437
    • Sandrini, F.1    Farmakidis, C.2    Kirschner, L.S.3    Wu, S.M.4    Tullio-Pelet, A.5    Lyonnet, S.6
  • 13
    • 0033133919 scopus 로고    scopus 로고
    • The WD-repeat: a common architecture for diverse functions
    • Smith T.F., Gaitatzes C., Saxena K., and Neer E.J. The WD-repeat: a common architecture for diverse functions. Trends Biochem Sci 24 (1999) 181-185
    • (1999) Trends Biochem Sci , vol.24 , pp. 181-185
    • Smith, T.F.1    Gaitatzes, C.2    Saxena, K.3    Neer, E.J.4
  • 14
    • 36348978046 scopus 로고    scopus 로고
    • The nuclear pore complex: disease associations and functional correlations
    • Cronshaw J.M., and Matunis M.J. The nuclear pore complex: disease associations and functional correlations. Trends Endocrinol Metab 15 (2004) 34-39
    • (2004) Trends Endocrinol Metab , vol.15 , pp. 34-39
    • Cronshaw, J.M.1    Matunis, M.J.2
  • 15
    • 0037947770 scopus 로고    scopus 로고
    • The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome
    • Cronshaw J.M., and Matunis M.J. The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome. Proc Natl Acad Sci USA 100 (2003) 5823-5827
    • (2003) Proc Natl Acad Sci USA , vol.100 , pp. 5823-5827
    • Cronshaw, J.M.1    Matunis, M.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.