PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse

[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.