PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse
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H. Peeters | N. Niikawa | A. Bairoch | Y. Nakamura | K. Devriendt | J. Fryns | E. Parthoens | M. Gewillig | P. Debeer | C. Huysmans | W. V. D. Ven | V. Wilquet | W. Ven
[1] A. Schinzel. Catalogue of Unbalanced Chromosome Aberrations in Man, 2nd Edition , 2004, Chromosome Research.
[2] A. Chajut,et al. Identification of a novel stress-responsive gene Hi95 involved in regulation of cell viability , 2002, Oncogene.
[3] Tom H. Pringle,et al. The human genome browser at UCSC. , 2002, Genome research.
[4] Mathew W. Wright,et al. The HUGO Gene Nomenclature Committee (HGNC) , 2001, Human Genetics.
[5] H. Peeters,et al. Recurrent involvement of chromosomal region 6q21 in heterotaxy. , 2001, American journal of medical genetics.
[6] C. V. Wright. Mechanisms of left-right asymmetry: what's right and what's left? , 2001, Developmental cell.
[7] M. Taira,et al. A Xenopus homolog of a human p53-activated gene, PA26, is specifically expressed in the notochord , 2001, Mechanisms of Development.
[8] N. Hukriede,et al. A study of Xlim1 function in the Spemann-Mangold organizer. , 2001, The International journal of developmental biology.
[9] Alexander F. Schier,et al. Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects , 2000, Nature Genetics.
[10] B. Birren,et al. Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region. , 1999, American journal of human genetics.
[11] P. Tam,et al. Experimental analysis of the emergence of left-right asymmetry of the body axis in early postimplantation mouse embryos. , 1999, Cellular and molecular biology.
[12] J. Belmont,et al. Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development. , 1999, American journal of human genetics.
[13] G. Annéren,et al. Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3). , 1999, American journal of medical genetics.
[14] R. Beddington,et al. Axis Development and Early Asymmetry in Mammals , 1999, Cell.
[15] Leonard Buckbinder,et al. PA26, a novel target of the p53 tumor suppressor and member of the GADD family of DNA damage and growth arrest inducible genes , 1999, Oncogene.
[16] M. Gebbia,et al. Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIB. , 1999, American journal of medical genetics.
[17] Clifford J. Tabin,et al. The Transfer of Left-Right Positional Information during Chick Embryogenesis , 1998, Cell.
[18] Yusuke Nakamura,et al. FISH mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia , 1997, The Japanese Journal of Human Genetics.
[19] D. Schlessinger,et al. X-linked situs abnormalities result from mutations in ZIC3 , 1997, Nature Genetics.
[20] N. Niikawa,et al. De novo balanced translocation (6 ; 18) (q21 ; q21.3) in a patient with heterotaxia , 1996 .
[21] H. Yost,et al. Role of notochord in specification of cardiac left-right orientation in zebrafish and Xenopus. , 1996, Developmental biology.
[22] E. Zackai,et al. Analysis of clinical variation seen in patients with 18q terminal deletions. , 1995, American journal of medical genetics.
[23] C. Tabin,et al. A molecular pathway determining left-right asymmetry in chick embryogenesis , 1995, Cell.
[24] S. S. Schneider,et al. The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2. , 1995, American journal of human genetics.
[25] Francis S. Collins,et al. Positional cloning moves from perditional to traditional , 1995, Nature Genetics.
[26] T. Jessell,et al. Floor plate and motor neuron induction by vhh-1, a vertebrate homolog of hedgehog expressed by the notochord , 1994, Cell.
[27] A. Ballabio,et al. Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1 , 1993, Nature Genetics.
[28] P. Devilee,et al. Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21. , 1986, Cytogenetics and cell genetics.