Connection

DAVID NELSON to Animals

This is a "connection" page, showing publications DAVID NELSON has written about Animals.
Connection Strength

0.858
  1. A near telomere-to-telomere phased reference assembly for the male mountain gorilla. Sci Data. 2025 May 22; 12(1):842.
    View in: PubMed
    Score: 0.052
  2. Ectopic expression of CGG-repeats alters ovarian response to gonadotropins and leads to infertility in a murine FMR1 premutation model. Hum Mol Genet. 2021 05 29; 30(10):923-938.
    View in: PubMed
    Score: 0.039
  3. The Fragile X proteins Fmrp and Fxr2p cooperate to regulate glucose metabolism in mice. Hum Mol Genet. 2015 Apr 15; 24(8):2175-84.
    View in: PubMed
    Score: 0.025
  4. CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome. Hum Mol Genet. 2014 Nov 15; 23(22):5906-15.
    View in: PubMed
    Score: 0.024
  5. The unstable repeats--three evolving faces of neurological disease. Neuron. 2013 Mar 06; 77(5):825-43.
    View in: PubMed
    Score: 0.022
  6. HlyU is a positive regulator of hemolysin expression in Vibrio anguillarum. J Bacteriol. 2011 Sep; 193(18):4779-89.
    View in: PubMed
    Score: 0.020
  7. Ectopic expression of CGG containing mRNA is neurotoxic in mammals. Hum Mol Genet. 2009 Jul 01; 18(13):2443-51.
    View in: PubMed
    Score: 0.017
  8. Altered hippocampal synaptic plasticity in the FMR1 gene family knockout mouse models. J Neurophysiol. 2009 May; 101(5):2572-80.
    View in: PubMed
    Score: 0.017
  9. The Drosophila FMRP and LARK RNA-binding proteins function together to regulate eye development and circadian behavior. J Neurosci. 2008 Oct 08; 28(41):10200-5.
    View in: PubMed
    Score: 0.016
  10. Fragile X-related proteins regulate mammalian circadian behavioral rhythms. Am J Hum Genet. 2008 Jul; 83(1):43-52.
    View in: PubMed
    Score: 0.016
  11. Identification and characterization of a repeat-in-toxin gene cluster in Vibrio anguillarum. Infect Immun. 2008 Jun; 76(6):2620-32.
    View in: PubMed
    Score: 0.016
  12. Argonaute-2-dependent rescue of a Drosophila model of FXTAS by FRAXE premutation repeat. Hum Mol Genet. 2007 Oct 01; 16(19):2326-32.
    View in: PubMed
    Score: 0.015
  13. NEMO, NFkappaB signaling and incontinentia pigmenti. Curr Opin Genet Dev. 2006 Jun; 16(3):282-8.
    View in: PubMed
    Score: 0.014
  14. Genetics. The critical region in trisomy 21. Science. 2004 Oct 22; 306(5696):619-21.
    View in: PubMed
    Score: 0.012
  15. Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo. Hum Mol Genet. 2004 Jul 01; 13(13):1291-302.
    View in: PubMed
    Score: 0.012
  16. The truth about mouse, human, worms and yeast. Hum Genomics. 2004 Jan; 1(2):146-9.
    View in: PubMed
    Score: 0.012
  17. Human genetics. Primate shadow play. Science. 2003 Feb 28; 299(5611):1331-3.
    View in: PubMed
    Score: 0.011
  18. FMR2 function: insight from a mouse knockout model. Cytogenet Genome Res. 2003; 100(1-4):129-39.
    View in: PubMed
    Score: 0.011
  19. Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice. Genomics. 2002 Oct; 80(4):423-32.
    View in: PubMed
    Score: 0.011
  20. LLPS of FXR1 drives spermiogenesis by activating translation of stored mRNAs. Science. 2022 08 12; 377(6607):eabj6647.
    View in: PubMed
    Score: 0.011
  21. Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proc Natl Acad Sci U S A. 2022 05 31; 119(22):e2118124119.
    View in: PubMed
    Score: 0.011
  22. Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice. J Neurosci. 2002 Apr 01; 22(7):2753-63.
    View in: PubMed
    Score: 0.010
  23. Complex SNP-based haplotypes in three human helicases: implications for cancer association studies. Genome Res. 2002 Apr; 12(4):627-39.
    View in: PubMed
    Score: 0.010
  24. Intercepting IRE1 kinase-FMRP signaling prevents atherosclerosis progression. EMBO Mol Med. 2022 04 07; 14(4):e15344.
    View in: PubMed
    Score: 0.010
  25. Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28. Genomics. 2002 Jan; 79(1):31-40.
    View in: PubMed
    Score: 0.010
  26. Functional consequences of postnatal interventions in a mouse model of Fragile X syndrome. Neurobiol Dis. 2022 01; 162:105577.
    View in: PubMed
    Score: 0.010
  27. Comparative genomic sequence analysis of the FXR gene family: FMR1, FXR1, and FXR2. Genomics. 2001 Dec; 78(3):169-77.
    View in: PubMed
    Score: 0.010
  28. The genome of the stable fly, Stomoxys calcitrans, reveals potential mechanisms underlying reproduction, host interactions, and novel targets for pest control. BMC Biol. 2021 03 10; 19(1):41.
    View in: PubMed
    Score: 0.010
  29. Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium. Am J Hum Genet. 2000 Dec; 67(6):1437-51.
    View in: PubMed
    Score: 0.009
  30. (Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features. Hum Mol Genet. 2000 May 01; 9(8):1145-59.
    View in: PubMed
    Score: 0.009
  31. Deletion of Fmr1 from Forebrain Excitatory Neurons Triggers Abnormal Cellular, EEG, and Behavioral Phenotypes in the Auditory Cortex of a Mouse Model of Fragile X Syndrome. Cereb Cortex. 2020 03 14; 30(3):969-988.
    View in: PubMed
    Score: 0.009
  32. Brown marmorated stink bug, Halyomorpha halys (St?l), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest. BMC Genomics. 2020 Mar 14; 21(1):227.
    View in: PubMed
    Score: 0.009
  33. Alternative splicing in the murine and human FXR1 genes. Genomics. 1999 Jul 15; 59(2):193-202.
    View in: PubMed
    Score: 0.009
  34. Metabolic pathways modulate the neuronal toxicity associated with fragile X-associated tremor/ataxia syndrome. Hum Mol Genet. 2019 03 15; 28(6):980-991.
    View in: PubMed
    Score: 0.008
  35. Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy. Nat Commun. 2019 02 15; 10(1):797.
    View in: PubMed
    Score: 0.008
  36. Firefly genomes illuminate parallel origins of bioluminescence in beetles. Elife. 2018 10 16; 7.
    View in: PubMed
    Score: 0.008
  37. Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees. Genomics. 1998 Jun 15; 50(3):368-72.
    View in: PubMed
    Score: 0.008
  38. Blooming of Unusual Cytochrome P450s by Tandem Duplication in the Pathogenic Fungus Conidiobolus coronatus. Int J Mol Sci. 2018 06 09; 19(6).
    View in: PubMed
    Score: 0.008
  39. FXR-Gankyrin axis is involved in development of pediatric liver cancer. Carcinogenesis. 2017 07 01; 38(7):738-747.
    View in: PubMed
    Score: 0.008
  40. The draft genome of whitefly Bemisia tabaci MEAM1, a global crop pest, provides novel insights into virus transmission, host adaptation, and insecticide resistance. BMC Biol. 2016 12 14; 14(1):110.
    View in: PubMed
    Score: 0.007
  41. Genome of the Asian longhorned beetle (Anoplophora glabripennis), a globally significant invasive species, reveals key functional and evolutionary innovations at the beetle-plant interface. Genome Biol. 2016 11 11; 17(1):227.
    View in: PubMed
    Score: 0.007
  42. Molecular evolutionary dynamics of cytochrome P450 monooxygenases across kingdoms: Special focus on mycobacterial P450s. Sci Rep. 2016 09 12; 6:33099.
    View in: PubMed
    Score: 0.007
  43. Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo. J Neurosci. 2016 07 06; 36(27):7079-94.
    View in: PubMed
    Score: 0.007
  44. Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution. Hum Mol Genet. 1996 Jul; 5(7):899-912.
    View in: PubMed
    Score: 0.007
  45. Insights into Adaptations to a Near-Obligate Nematode Endoparasitic Lifestyle from the Finished Genome of Drechmeria coniospora. Sci Rep. 2016 Mar 15; 6:23122.
    View in: PubMed
    Score: 0.007
  46. Genomic insights into the Ixodes scapularis tick vector of Lyme disease. Nat Commun. 2016 Feb 09; 7:10507.
    View in: PubMed
    Score: 0.007
  47. Unique features of a global human ectoparasite identified through sequencing of the bed bug genome. Nat Commun. 2016 Feb 02; 7:10165.
    View in: PubMed
    Score: 0.007
  48. Evolution of the cryptic FMR1 CGG repeat. Nat Genet. 1995 Nov; 11(3):301-8.
    View in: PubMed
    Score: 0.007
  49. Diversity and evolution of cytochrome P450 monooxygenases in Oomycetes. Sci Rep. 2015 Jul 01; 5:11572.
    View in: PubMed
    Score: 0.007
  50. Positional cloning reaches maturity. Curr Opin Genet Dev. 1995 Jun; 5(3):298-303.
    View in: PubMed
    Score: 0.006
  51. The fragile X syndromes. Semin Cell Biol. 1995 Feb; 6(1):5-11.
    View in: PubMed
    Score: 0.006
  52. The GABAA receptor is an FMRP target with therapeutic potential in fragile X syndrome. Cell Cycle. 2015; 14(18):2985-95.
    View in: PubMed
    Score: 0.006
  53. FXR1P limits long-term memory, long-lasting synaptic potentiation, and de novo GluA2 translation. Cell Rep. 2014 Nov 20; 9(4):1402-1416.
    View in: PubMed
    Score: 0.006
  54. Origin of the response to adrenal and sex steroids: Roles of promiscuity and co-evolution of enzymes and steroid receptors. J Steroid Biochem Mol Biol. 2015 Jul; 151:12-24.
    View in: PubMed
    Score: 0.006
  55. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE. Nat Genet. 1994 Nov; 8(3):229-35.
    View in: PubMed
    Score: 0.006
  56. Genome of the house fly, Musca domestica L., a global vector of diseases with adaptations to a septic environment. Genome Biol. 2014; 15(10):466.
    View in: PubMed
    Score: 0.006
  57. Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome. Hum Mol Genet. 2014 Feb 15; 23(4):1095-107.
    View in: PubMed
    Score: 0.006
  58. Homeostatic responses fail to correct defective amygdala inhibitory circuit maturation in fragile X syndrome. J Neurosci. 2013 Apr 24; 33(17):7548-58.
    View in: PubMed
    Score: 0.006
  59. The African coelacanth genome provides insights into tetrapod evolution. Nature. 2013 Apr 18; 496(7445):311-6.
    View in: PubMed
    Score: 0.006
  60. Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration. Proc Natl Acad Sci U S A. 2013 May 07; 110(19):7778-83.
    View in: PubMed
    Score: 0.006
  61. Bmal1 and ?-cell clock are required for adaptation to circadian disruption, and their loss of function leads to oxidative stress-induced ?-cell failure in mice. Mol Cell Biol. 2013 Jun; 33(11):2327-38.
    View in: PubMed
    Score: 0.006
  62. Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neurodegeneration in Drosophila. Hum Mol Genet. 2012 May 01; 21(9):2068-75.
    View in: PubMed
    Score: 0.005
  63. FXR1P but not FMRP regulates the levels of mammalian brain-specific microRNA-9 and microRNA-124. J Neurosci. 2011 Sep 28; 31(39):13705-9.
    View in: PubMed
    Score: 0.005
  64. Retrotransposon activation contributes to fragile X premutation rCGG-mediated neurodegeneration. Hum Mol Genet. 2012 Jan 01; 21(1):57-65.
    View in: PubMed
    Score: 0.005
  65. Expression of an IRF-3 fusion protein and mouse estrogen receptor, inhibits hepatitis C viral replication in RIG-I-deficient Huh 7.5 cells. Virol J. 2011 Sep 21; 8:445.
    View in: PubMed
    Score: 0.005
  66. Desmoplakin and talin2 are novel mRNA targets of fragile X-related protein-1 in cardiac muscle. Circ Res. 2011 Jul 22; 109(3):262-71.
    View in: PubMed
    Score: 0.005
  67. Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning. Nat Med. 2011 May; 17(5):559-65.
    View in: PubMed
    Score: 0.005
  68. AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome. Neurobiol Dis. 2011 Jun; 42(3):311-7.
    View in: PubMed
    Score: 0.005
  69. Site-specific phosphorylation of the middle molecular weight human neurofilament protein in transfected non-neuronal cells. J Neurosci. 1990 Jul; 10(7):2428-37.
    View in: PubMed
    Score: 0.005
  70. The Ectocarpus genome and the independent evolution of multicellularity in brown algae. Nature. 2010 Jun 03; 465(7298):617-21.
    View in: PubMed
    Score: 0.005
  71. Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons. Neurobiol Dis. 2009 Aug; 35(2):241-50.
    View in: PubMed
    Score: 0.004
  72. Reversal of sensorimotor gating abnormalities in Fmr1 knockout mice carrying a human Fmr1 transgene. Behav Neurosci. 2008 Dec; 122(6):1371-7.
    View in: PubMed
    Score: 0.004
  73. Social behavior in Fmr1 knockout mice carrying a human FMR1 transgene. Behav Neurosci. 2008 Jun; 122(3):710-5.
    View in: PubMed
    Score: 0.004
  74. Impaired hippocampal synaptic function in secretin deficient mice. Neuroscience. 2008 Jul 17; 154(4):1417-22.
    View in: PubMed
    Score: 0.004
  75. Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice. Neurobiol Dis. 2008 Jul; 31(1):127-32.
    View in: PubMed
    Score: 0.004
  76. The Physcomitrella genome reveals evolutionary insights into the conquest of land by plants. Science. 2008 Jan 04; 319(5859):64-9.
    View in: PubMed
    Score: 0.004
  77. The Chlamydomonas genome reveals the evolution of key animal and plant functions. Science. 2007 Oct 12; 318(5848):245-50.
    View in: PubMed
    Score: 0.004
  78. RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS. Neuron. 2007 Aug 16; 55(4):565-71.
    View in: PubMed
    Score: 0.004
  79. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation. Exp Cell Res. 2007 Jan 15; 313(2):244-53.
    View in: PubMed
    Score: 0.004
  80. Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior. Hum Mol Genet. 2006 Nov 01; 15(21):3241-50.
    View in: PubMed
    Score: 0.004
  81. Audiogenic seizure susceptibility is reduced in fragile X knockout mice after introduction of FMR1 transgenes. Exp Neurol. 2007 Jan; 203(1):233-40.
    View in: PubMed
    Score: 0.004
  82. Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins. Hum Mol Genet. 2006 Jun 15; 15(12):1984-94.
    View in: PubMed
    Score: 0.003
  83. The finished DNA sequence of human chromosome 12. Nature. 2006 03 16; 440(7082):346-51.
    View in: PubMed
    Score: 0.003
  84. Eucaryotic chromosome transfer: production of a murine-specific cosmid library from a neor-linked fragment of murine chromosome 17. Mol Cell Biol. 1986 Feb; 6(2):441-51.
    View in: PubMed
    Score: 0.003
  85. Gene replacement therapy for inborn errors of purine metabolism. Cold Spring Harb Symp Quant Biol. 1986; 51 Pt 2:1065-71.
    View in: PubMed
    Score: 0.003
  86. The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo. Neurobiol Dis. 2006 Mar; 21(3):549-55.
    View in: PubMed
    Score: 0.003
  87. Novel type I interferon IL-28A suppresses hepatitis C viral RNA replication. Virol J. 2005 Sep 07; 2:80.
    View in: PubMed
    Score: 0.003
  88. Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome. Neuron. 2005 Aug 04; 47(3):339-52.
    View in: PubMed
    Score: 0.003
  89. The DNA sequence of the human X chromosome. Nature. 2005 Mar 17; 434(7031):325-37.
    View in: PubMed
    Score: 0.003
  90. Stabilized beta-catenin promotes hepatocyte proliferation and inhibits TNFalpha-induced apoptosis. Lab Invest. 2004 Mar; 84(3):332-41.
    View in: PubMed
    Score: 0.003
  91. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nat Neurosci. 2004 Feb; 7(2):113-7.
    View in: PubMed
    Score: 0.003
  92. Metaphase chromosome transfer of introduced selectable markers. J Mol Appl Genet. 1984; 2(6):563-77.
    View in: PubMed
    Score: 0.003
  93. Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain. Neuron. 2002 Jun 13; 34(6):961-72.
    View in: PubMed
    Score: 0.003
  94. Knockout mouse model for Fxr2: a model for mental retardation. Hum Mol Genet. 2002 Mar 01; 11(5):487-98.
    View in: PubMed
    Score: 0.003
  95. Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes. Hum Mol Genet. 2001 Oct 15; 10(22):2557-67.
    View in: PubMed
    Score: 0.003
  96. Initial sequencing and analysis of the human genome. Nature. 2001 Feb 15; 409(6822):860-921.
    View in: PubMed
    Score: 0.002
  97. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet. 2000 Oct; 26(2):191-4.
    View in: PubMed
    Score: 0.002
  98. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins. Hum Mol Genet. 2000 Jun 12; 9(10):1487-93.
    View in: PubMed
    Score: 0.002
  99. Proposal for a human genome evolution project. Mol Phylogenet Evol. 2000 Apr; 15(1):1-4.
    View in: PubMed
    Score: 0.002
  100. The genome sequence of Drosophila melanogaster. Science. 2000 Mar 24; 287(5461):2185-95.
    View in: PubMed
    Score: 0.002
  101. Human homologue of the murine bare patches/striated gene is not mutated in incontinentia pigmenti type 2. Am J Med Genet. 2000 Mar 20; 91(3):241-4.
    View in: PubMed
    Score: 0.002
  102. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Hum Mol Genet. 1998 Nov; 7(12):1935-46.
    View in: PubMed
    Score: 0.002
  103. A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence. Proc Natl Acad Sci U S A. 1998 Sep 29; 95(20):11751-6.
    View in: PubMed
    Score: 0.002
  104. MSG1 (melanocyte-specific gene 1): mapping to chromosome Xq13.1, genomic organization, and promoter analysis. Genomics. 1998 Aug 01; 51(3):401-7.
    View in: PubMed
    Score: 0.002
  105. Overexpression of the human NFM subunit in transgenic mice modifies the level of endogenous NFL and the phosphorylation state of NFH subunits. J Cell Biol. 1995 Jun; 129(6):1629-40.
    View in: PubMed
    Score: 0.002
  106. The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney. Genomics. 1995 Jan 20; 25(2):462-8.
    View in: PubMed
    Score: 0.002
  107. Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat. Nat Genet. 1993 Jul; 4(3):244-51.
    View in: PubMed
    Score: 0.001
  108. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nat Genet. 1993 Jan; 3(1):36-43.
    View in: PubMed
    Score: 0.001
  109. Genome analysis and the human X chromosome. Science. 1992 Oct 02; 258(5079):103-9.
    View in: PubMed
    Score: 0.001
  110. Cloning of human and bovine homologs of SNF2/SWI2: a global activator of transcription in yeast S. cerevisiae. Nucleic Acids Res. 1992 Sep 11; 20(17):4649-55.
    View in: PubMed
    Score: 0.001
  111. PCR amplification and analysis of yeast artificial chromosomes. Genomics. 1992 Aug; 13(4):1303-6.
    View in: PubMed
    Score: 0.001
  112. Direct cloning of human transcripts with HnRNA from hybrid cell lines. Science. 1990 Aug 10; 249(4969):652-5.
    View in: PubMed
    Score: 0.001
  113. Report of the X chromosome workshop. Genomics. 1990 Aug; 7(4):647-54.
    View in: PubMed
    Score: 0.001
  114. The large DNA insert cloning workshop. Genomics. 1990 Aug; 7(4):654-60.
    View in: PubMed
    Score: 0.001
  115. Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction. Genomics. 1990 Mar; 6(3):475-81.
    View in: PubMed
    Score: 0.001
  116. Chromosome-mediated transfer of the murine Na,K-ATPase alpha subunit confers ouabain resistance. Mol Cell Biol. 1987 Aug; 7(8):2985-7.
    View in: PubMed
    Score: 0.001
  117. Eukaryotic chromosome transfer: linkage of the murine major histocompatibility complex to an inserted dominant selectable marker. Proc Natl Acad Sci U S A. 1984 Aug; 81(15):4879-83.
    View in: PubMed
    Score: 0.001
  118. Expression and regulation of human low-density lipoprotein receptors in Chinese hamster ovary cells. Nature. 1984 Feb 23-29; 307(5953):742-5.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.