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Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1.
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Conservation of synteny between the genome of the pufferfish (Fugu rubripes) and the region on human chromosome 14 (14q24.3) associated with familial Alzheimer disease (AD3 locus).
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Genomic sequence analysis of Fugu rubripes CFTR and flanking genes in a 60 kb region conserving synteny with 800 kb of human chromosome 7.
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The neural cell adhesion molecule L1: genomic organisation and differential splicing is conserved between man and the pufferfish Fugu.
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Analysis of the dopamine receptor family in the compact genome of the puffer fish Fugu rubripes.
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Molecular cloning of EDG-3 and N-Shc genes from the puffer fish, Fugu rubripes, and conservation of synteny with the human genome.
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Quality not quantity: the pufferfish genome.
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Analysis of the conservation of synteny between Fugu and human chromosome 12.
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Fugu and human sequence comparison identifies novel human genes and conserved non-coding sequences.
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The comparative genomic structure and sequence of the surfeit gene homologs in the puffer fish Fugu rubripes and their association with CpG-rich islands.
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Repertoire of Protein Kinases Encoded in the Genome of Takifugu rubripes.
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Kinetoplastid PPEF phosphatases: dual acylated proteins expressed in the endomembrane system of Leishmania.
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Genomic analysis of a 1 Mb region near the telomere of Hessian fly chromosome X2 and avirulence gene vH13.
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CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms.
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Rett syndrome: clinical review and genetic update.
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Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.
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Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation.
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Conservation of long-range synteny and microsynteny between the genomes of two distantly related nematodes.
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Four-hundred million years of conserved synteny of human Xp and Xq genes on three Tetraodon chromosomes.
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Molecular cloning and characterization of the Fugu rubripes MEST/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridis.
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CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP.
Evolution. 1985 Jul;39(4):783-791. doi: 10.1111/j.1558-5646.1985.tb00420.x.
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Complete sequencing of the Fugu WAGR region from WT1 to PAX6: dramatic compaction and conservation of synteny with human chromosome 11p13.
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Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region.
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Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes.
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The comparative genomic structure and sequence of the surfeit gene homologs in the puffer fish Fugu rubripes and their association with CpG-rich islands.
Genome Res. 1997 Dec;7(12):1138-52. doi: 10.1101/gr.7.12.1138.
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Cloning and sequencing of complement component C9 and its linkage to DOC-2 in the pufferfish Fugu rubripes.
Gene. 1997 Oct 24;200(1-2):203-11. doi: 10.1016/s0378-1119(97)00423-x.
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Transgenic rats reveal functional conservation of regulatory controls between the Fugu isotocin and rat oxytocin genes.
Proc Natl Acad Sci U S A. 1997 Nov 11;94(23):12462-6. doi: 10.1073/pnas.94.23.12462.
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Regions of human chromosome 2 (2q32-q35) and mouse chromosome 1 show synteny with the pufferfish genome (Fugu rubripes).
Genomics. 1997 Oct 1;45(1):158-67. doi: 10.1006/geno.1997.4913.
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Positional cloning of the gene associated with X-linked juvenile retinoschisis.
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Identification and characterization of a conserved family of protein serine/threonine phosphatases homologous to Drosophila retinal degeneration C.
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