메뉴 건너뛰기




Volumn 40, Issue 4, 2003, Pages 249-256

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: An imprinted candidate for Silver-Russell syndrome

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYPEPTIDASE A; CARBOXYPEPTIDASE A1; CARBOXYPEPTIDASE A2; CARBOXYPEPTIDASE A4; CARBOXYPEPTIDASE A5; UNCLASSIFIED DRUG; CARBOXYPEPTIDASE; COMPLEMENTARY DNA; CPA5 PROTEIN, HUMAN; DNA;

EID: 0037374845     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.40.4.249     Document Type: Article
Times cited : (44)

References (42)
  • 4
    • 78651048074 scopus 로고
    • Syndrome of congenital hemihypertrophy, short stature and elevated urinary gonadotrophins
    • Silver H, Kiyasu W, Geirge J, Deamer W. Syndrome of congenital hemihypertrophy, short stature and elevated urinary gonadotrophins. Pediatrics 1953;12:368-76.
    • (1953) Pediatrics , vol.12 , pp. 368-376
    • Silver, H.1    Kiyasu, W.2    Geirge, J.3    Deamer, W.4
  • 5
    • 0000771975 scopus 로고
    • A syndrome of "intrauterine dwarfism" recognised at birth with cranio-facial dysostosis, disproportionally short arms, and other anomalies
    • Russell A. A syndrome of "intrauterine dwarfism" recognised at birth with cranio-facial dysostosis, disproportionally short arms, and other anomalies. Proc R Soc Med 1954;47:1040-4.
    • (1954) Proc R Soc Med , vol.47 , pp. 1040-1044
    • Russell, A.1
  • 6
    • 0032758850 scopus 로고    scopus 로고
    • The spectrum of Silver-Russell syndrome: A clinical and molecular genetic study and new diagnostic criteria
    • Price S, Stanhope R, Garet C, Preece M, Trembath. The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria. J Med Genet 1999;36:837-42.
    • (1999) J Med Genet , vol.36 , pp. 837-842
    • Price, S.1    Stanhope, R.2    Garet, C.3    Preece, M.4    Trembath5
  • 8
    • 0031568867 scopus 로고    scopus 로고
    • Assignment of growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12
    • Jerome CA, Scherer SW, Tsui LC, Gietz RD, Triggs-Raine B. Assignment of growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12. Genomics 1997;40:215-16.
    • (1997) Genomics , vol.40 , pp. 215-216
    • Jerome, C.A.1    Scherer, S.W.2    Tsui, L.C.3    Gietz, R.D.4    Triggs-Raine, B.5
  • 11
    • 0035131431 scopus 로고    scopus 로고
    • Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome
    • Hitchins MP, Monk D, Bell GM, Ali Z, Preece MA, Stanier P, Moore GE. Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome. Eur J Hum Genet 2001;9:82-90.
    • (2001) Eur J Hum Genet , vol.9 , pp. 82-90
    • Hitchins, M.P.1    Monk, D.2    Bell, G.M.3    Ali, Z.4    Preece, M.A.5    Stanier, P.6    Moore, G.E.7
  • 12
    • 0035870563 scopus 로고    scopus 로고
    • A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21
    • Ono, R, Kobayashi S, Wagatsuma H, Aisaka K, Kohda T, Kaneko-Ishino T, Ishino F. A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21. Genomics 2001;73:232-7.
    • (2001) Genomics , vol.73 , pp. 232-237
    • Ono, R.1    Kobayashi, S.2    Wagatsuma, H.3    Aisaka, K.4    Kohda, T.5    Kaneko-Ishino, T.6    Ishino, F.7
  • 18
    • 0035168178 scopus 로고    scopus 로고
    • A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region
    • Hannula K, Lipsanen-Nyman M, Kontiokari T, Kere J. A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver. Russell syndrome delimits a candidate gene region. Am J Hum Genet 2001;68:247-53.
    • (2001) Am J Hum Genet , vol.68 , pp. 247-253
    • Hannula, K.1    Lipsanen-Nyman, M.2    Kontiokari, T.3    Kere, J.4
  • 19
    • 0031687985 scopus 로고    scopus 로고
    • Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
    • Lefebvre L, Viville S, Barton SC, Ishino F, Keverne EB, Surani MA. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet 1998;20:163-9.
    • (1998) Nat Genet , vol.20 , pp. 163-169
    • Lefebvre, L.1    Viville, S.2    Barton, S.C.3    Ishino, F.4    Keverne, E.B.5    Surani, M.A.6
  • 22
    • 0034534937 scopus 로고    scopus 로고
    • Peg1/Mest locates distal to the currently defined imprinting region on mouse proximal chromosome 6 and identifies a new imprinting region affecting growth
    • Beechey CV. Peg1/Mest locates distal to the currently defined imprinting region on mouse proximal chromosome 6 and identifies a new imprinting region affecting growth. Cytogenet Cell Genet 2000;90:309-14.
    • (2000) Cytogenet Cell Genet , vol.90 , pp. 309-314
    • Beechey, C.V.1
  • 23
    • 0035200832 scopus 로고    scopus 로고
    • Carboxypeptidases from A to Z: Implications in embryonic development and Wnt binding
    • Reznik SE, Fricker LD. Carboxypeptidases from A to Z: implications in embryonic development and Wnt binding. Cell Mol Life Sci 2001;58:1790-804.
    • (2001) Cell Mol Life Sci , vol.58 , pp. 1790-1804
    • Reznik, S.E.1    Fricker, L.D.2
  • 24
    • 0037177891 scopus 로고    scopus 로고
    • Identification and characterization of three members of the human metallocarboxypeptidase gene family
    • Wei S, Segura S, Vendrell J, Aviles FX, Lanoue E, Day R, Feng Y, Fricker LD. Identification and characterization of three members of the human metallocarboxypeptidase gene family. J Biol Chem 2002;277:14954-64.
    • (2002) J Biol Chem , vol.277 , pp. 14954-14964
    • Wei, S.1    Segura, S.2    Vendrell, J.3    Aviles, F.X.4    Lanoue, E.5    Day, R.6    Feng, Y.7    Fricker, L.D.8
  • 25
    • 0029099808 scopus 로고
    • Carboxypeptidase A isoforms produced by distinct genes or alternative splicing in brain and other extrapancreatic tissues
    • Normant E, Gros C, Schwartz JC. Carboxypeptidase A isoforms produced by distinct genes or alternative splicing in brain and other extrapancreatic tissues. J Biol Chem 1995;270:20543-9.
    • (1995) J Biol Chem , vol.270 , pp. 20543-20549
    • Normant, E.1    Gros, C.2    Schwartz, J.C.3
  • 26
    • 0033564458 scopus 로고    scopus 로고
    • Carboxypeptidase A3 (CPA3): A novel gene highly induced by histone deacetylase inhibitors during differentiation of prostate epithelial cancer cells
    • Huang H, Reed CP, Zhang JS, Shridhar V, Wang L, Smith DI. Carboxypeptidase A3 (CPA3): a novel gene highly induced by histone deacetylase inhibitors during differentiation of prostate epithelial cancer cells. Cancer Res 1999;59:2981-98.
    • (1999) Cancer Res , vol.59 , pp. 2981-2998
    • Huang, H.1    Reed, C.P.2    Zhang, J.S.3    Shridhar, V.4    Wang, L.5    Smith, D.I.6
  • 33
    • 0034117095 scopus 로고    scopus 로고
    • Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability
    • Hellman A, Rahat A, Scherer SW, Darvasi A, Tsui LC, Kerem B. Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability. Mol Cell Biol 2000;20:4420-27.
    • (2000) Mol Cell Biol , vol.20 , pp. 4420-4427
    • Hellman, A.1    Rahat, A.2    Scherer, S.W.3    Darvasi, A.4    Tsui, L.C.5    Kerem, B.6
  • 35
    • 0030920665 scopus 로고    scopus 로고
    • Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1
    • Nishiwaki K, Niikawa N, Ishikawa M. Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1. Jpn J Hum Genet 1997;42:205-11.
    • (1997) Jpn J Hum Genet , vol.42 , pp. 205-211
    • Nishiwaki, K.1    Niikawa, N.2    Ishikawa, M.3
  • 37
    • 0029950244 scopus 로고    scopus 로고
    • Polymorphic functional imprinting of the human IGF2 gene among individuals, in blood cells, is associated with H19 expression
    • Giannoukakis N, Deal C, Paquette J, Kukuvitis A, Polychronakos C. Polymorphic functional imprinting of the human IGF2 gene among individuals, in blood cells, is associated with H19 expression. Biochem Biophys Res Commun 1996;220:1014-19.
    • (1996) Biochem Biophys Res Commun , vol.220 , pp. 1014-1019
    • Giannoukakis, N.1    Deal, C.2    Paquette, J.3    Kukuvitis, A.4    Polychronakos, C.5
  • 38
    • 0027716060 scopus 로고    scopus 로고
    • Functional polymorphism in the parental imprinting of the human IGF2R gene
    • Xu Y, Goodyer CG, Deal C, Polychronakos C. Functional polymorphism in the parental imprinting of the human IGF2R gene. Biochem Biophys Res Commun 1997;197:747-54.
    • (1997) Biochem Biophys Res Commun , vol.197 , pp. 747-754
    • Xu, Y.1    Goodyer, C.G.2    Deal, C.3    Polychronakos, C.4
  • 40
    • 0001076782 scopus 로고
    • Parent-specific gene expression and the triploid endosperm
    • Haig D, Westoby M. Parent-specific gene expression and the triploid endosperm. Am Natruralist 1989;134:147-55.
    • (1989) Am Natruralist , vol.134 , pp. 147-155
    • Haig, D.1    Westoby, M.2
  • 42
    • 0034210726 scopus 로고    scopus 로고
    • Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32
    • Hayashida S, Yamasaki K, Asada Y, Soeda E, Niikawa N, Kishino T. Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32. Genomics 2000;66:221-5.
    • (2000) Genomics , vol.66 , pp. 221-225
    • Hayashida, S.1    Yamasaki, K.2    Asada, Y.3    Soeda, E.4    Niikawa, N.5    Kishino, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.