Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1. Lim J, Crespo-Barreto J, Jafar-Nejad P, Bowman AB, Richman R, Hill DE, Orr HT, Zoghbi HY (2008) Nature 452: 713-8 CAG trinucleotide RNA repeats interact with RNA-binding proteins. McLaughlin BA, Spencer C, Eberwine J (1996) Am J Hum Genet 59: 561-9 Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range. Sullivan AK, Crawford DC, Scott EH, Leslie ML, Sherman SL (2002) Am J Hum Genet 70: 1532-44 Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population. Crawford DC, Schwartz CE, Meadows KL, Newman JL, Taft LF, Gunter C, Brown WT, Carpenter NJ, Howard-Peebles PN, Monaghan KG, Nolin SL, Reiss AL, Feldman GL, Rohlfs EM, Warren ST, Sherman SL (2000) Am J Hum Genet 66: 480-93 Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model. Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD, Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B (2004) Hum Mol Genet 13: 2841-51 Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability. Crawford DC, Zhang F, Wilson B, Warren ST, Sherman SL (2000) Hum Mol Genet 9: 1759-69 Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR. Crawford DC, Wilson B, Sherman SL (2000) Hum Mol Genet 9: 2909-18 Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST (1998) Hum Mol Genet 7: 1935-46 Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle. Yamagata K, Takeda J, Menzel S, Chen X, Eng S, Lim LR, Concannon P, Hanis CL, Spielman RS, Cox NJ, Bell GI (1996) Diabetologia 39: 725-30 The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansion. Loyd JE, Slovis B, Phillips JA, Butler MG, Foroud TM, Conneally PM, Newman JH (1997) Chest 111: 82S-83S FMR1 and the fragile X syndrome: human genome epidemiology review. Crawford DC, Acuña JM, Sherman SL (2001) Genet Med 3: 359-71 A case-based evaluation of SRD5A1, SRD5A2, AR, and ADRA1A as candidate genes for severity of BPH. Klotsman M, Weinberg CR, Davis K, Binnie CG, Hartmann KE (2004) Pharmacogenomics J 4: 251-9 The exocyclic 1,N2-deoxyguanosine pyrimidopurinone M1G is a chemically stable DNA adduct when placed opposite a two-base deletion in the (CpG)3 frameshift hotspot of the Salmonella typhimurium hisD3052 gene. Schnetz-Boutaud NC, Saleh S, Marnett LJ, Stone MP (2001) Biochemistry 40: 15638-49 Steroid hormones and hormone-related genetic and lifestyle characteristics as risk factors for benign prostatic hyperplasia: review of epidemiologic literature. Neuhouser ML, Kristal AR, Penson DF (2004) Urology 64: 201-11 Fragile X gene premutation in multiple system atrophy. Garland EM, Vnencak-Jones CL, Biaggioni I, Davis TL, Montine TJ, Robertson D (2004) J Neurol Sci 227: 115-8 Clear cell sarcoma or malignant melanoma of soft parts: molecular analysis of microsatellite instability with clinical correlation. Aue G, Hedges LK, Schwartz HS, Bridge JA, Neff JR, Butler MG (1998) Cancer Genet Cytogenet 105: 24-8
Hints: (1) double-click or double-tap to navigate to a node. (2) Grab a node and move it to arrange the graph.