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GENE - TERM ANNOTATION REPORT

20 Annotations Found.

An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(EXP) inferred from experiment]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:2137202 PMID:2215617 PMID:9020854 PMID:9391065 PMID:16737970 PMID:18273801 PMID:19206210 PMID:28715844


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Pinto LH, etal., Vis Neurosci. 2005 Sep-Oct;22(5):619-29.
  • The annotation has been inferred from sequence orthology with Rho (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Pinto LH, etal., Vis Neurosci. 2005 Sep-Oct;22(5):619-29.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: DNA:missense mutation: :p.Y110C (mouse)


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Sancho-Pelluz J, etal., Mol Med. 2012 May 9;18:549-55. doi: 10.2119/molmed.2011.00475.
  • The annotation has been inferred from sequence orthology with Rho (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Sancho-Pelluz J, etal., Mol Med. 2012 May 9;18:549-55. doi: 10.2119/molmed.2011.00475.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Mussolino C, etal., EMBO Mol Med. 2011 Mar;3(3):118-28. doi: 10.1002/emmm.201000119. Epub 2011 Jan 26.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Mussolino C, etal., EMBO Mol Med. 2011 Mar;3(3):118-28. doi: 10.1002/emmm.201000119. Epub 2011 Jan 26.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Qualifier: treatment


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Azam M, etal., Mol Vis. 2009 Dec 3;15:2526-34.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 8 additional annotations were made from Azam M, etal., Mol Vis. 2009 Dec 3;15:2526-34.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: DNA:missense mutation:cds:c.448G>A (p.E150K) (human)


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Daiger SP, etal., Clin Genet. 2013 Aug;84(2):132-41. doi: 10.1111/cge.12203. Epub 2013 Jun 19.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(TAS) traceable author statement]
  • 152 additional annotations were made from Daiger SP, etal., Clin Genet. 2013 Aug;84(2):132-41. doi: 10.1111/cge.12203. Epub 2013 Jun 19.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Campbell M, etal., Exp Eye Res. 2006 Sep;83(3):484-92. Epub 2006 Apr 27.
  • The annotation has been inferred from sequence orthology with Rho (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Campbell M, etal., Exp Eye Res. 2006 Sep;83(3):484-92. Epub 2006 Apr 27.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Pan Z, etal., Mol Vis. 2012;18:3013-20. Epub 2012 Dec 14.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Pan Z, etal., Mol Vis. 2012;18:3013-20. Epub 2012 Dec 14.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: DNA:missense mutations:cds:505G>C (p.A169P), 1040C>A (p.P347Q) (human)


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Dryja TP, etal., N Engl J Med. 1990 Nov 8;323(19):1302-7.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Dryja TP, etal., N Engl J Med. 1990 Nov 8;323(19):1302-7.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: DNA:point mutation:exon:P23H, P347L, P347S, T58R


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Milla E, etal., Ophthalmic Genet. 1998 Sep;19(3):131-9.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 additional annotations were made from Milla E, etal., Ophthalmic Genet. 1998 Sep;19(3):131-9.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: DNA:missense mutation:exon:p.C110Y (human)


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Gorbatyuk M, etal., Exp Eye Res. 2007 Jan;84(1):44-52. Epub 2006 Nov 1.
  • The annotation has been inferred from sequence orthology with Rho (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Gorbatyuk M, etal., Exp Eye Res. 2007 Jan;84(1):44-52. Epub 2006 Nov 1.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Qualifier: treatment


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Mao H, etal., Hum Gene Ther. 2011 May;22(5):567-75. doi: 10.1089/hum.2010.140. Epub 2011 Mar 7.
  • The annotation has been inferred from sequence orthology with Rho (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Mao H, etal., Hum Gene Ther. 2011 May;22(5):567-75. doi: 10.1089/hum.2010.140. Epub 2011 Mar 7.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Qualifier: treatment


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Rivera-De la Parra D, etal., Gene. 2013 Apr 25;519(1):173-6. doi: 10.1016/j.gene.2013.01.048. Epub 2013 Feb 9.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 additional annotations were made from Rivera-De la Parra D, etal., Gene. 2013 Apr 25;519(1):173-6. doi: 10.1016/j.gene.2013.01.048. Epub 2013 Feb 9.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: DNA:missense mutation:cds:c.233A>T (p.N78I) (human)


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Choudhury S, etal., Cell Death Dis. 2013 Mar 7;4:e528. doi: 10.1038/cddis.2013.34.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6 additional annotations were made from Choudhury S, etal., Cell Death Dis. 2013 Mar 7;4:e528. doi: 10.1038/cddis.2013.34.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: DNA:missense mutation: :p.T17M (human)


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Maubaret C, etal., Mol Vis. 2012;18:581-7. Epub 2012 Mar 2.
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 additional annotations were made from Maubaret C, etal., Mol Vis. 2012;18:581-7. Epub 2012 Mar 2.
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: DNA:deletion:exon:c.614_622del (p.Y206_F208del) (human)


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant retinitis pigmentosa | ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant/Recessive | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:10521250 PMID:10967073 PMID:11094174 PMID:11139241 PMID:11141431 PMID:12660238 PMID:12860986 PMID:12871954 PMID:12966518 PMID:1301135 PMID:1303237 PMID:1484692 PMID:14971589 PMID:15126168 PMID:1580841 PMID:16123440 PMID:16737970 PMID:16767206 PMID:17014888 PMID:17488458 PMID:17576681 PMID:1765377 PMID:1783387 PMID:18175313 PMID:1833777 PMID:1840561 PMID:1862076 PMID:1882937 PMID:1897520 PMID:19085385 PMID:1924344 PMID:19913029 PMID:19960070 PMID:20164459 PMID:20525296 PMID:20555336 PMID:20591486 PMID:21077204 PMID:21094163 PMID:21174529 PMID:21217109 PMID:21219898 PMID:21352497 PMID:21357407 PMID:21922596 PMID:2215617 PMID:22164218 PMID:22252712 PMID:22791210 PMID:22968130 PMID:22995991 PMID:23221340 PMID:23591405 PMID:23625926 PMID:24106275 PMID:24265693 PMID:24520188 PMID:24760071 PMID:24935155 PMID:24938718 PMID:2509724 PMID:25097241 PMID:25101269 PMID:25221422 PMID:25408095 PMID:25525159 PMID:25741868 PMID:25999674 PMID:26887858 PMID:26962691 PMID:28041643 PMID:28076437 PMID:28341476 PMID:28492532 PMID:28524165 PMID:28559085 PMID:28981474 PMID:29068140 PMID:29099798 PMID:29847639 PMID:29890221 PMID:30240733 PMID:30718709 PMID:30977563 PMID:31100078 PMID:31319082 PMID:31456290 PMID:31908405 PMID:32037395 PMID:32581362 PMID:33576794 PMID:34906470 PMID:36909829 PMID:7724183 PMID:7981701 PMID:7987326 PMID:7987331 PMID:7987385 PMID:8045708 PMID:8088850 PMID:8240107 PMID:8253795 PMID:8317502 PMID:8328469 PMID:8353500 PMID:8401533 PMID:8406457 PMID:8554077 PMID:8841304 PMID:8905849 PMID:9050844 PMID:9197578 PMID:9380676 PMID:9483582 PMID:9536098 PMID:9618546 PMID:9810568


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant retinitis pigmentosa | ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant/Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:10521250 PMID:10967073 PMID:11094174 PMID:11139241 PMID:12660238 PMID:12860986 PMID:12871954 PMID:12966518 PMID:1301135 PMID:1303237 PMID:1484692 PMID:14971589 PMID:1580841 PMID:16123440 PMID:16767206 PMID:17488458 PMID:17576681 PMID:1783387 PMID:18175313 PMID:1833777 PMID:1840561 PMID:1862076 PMID:1882937 PMID:1897520 PMID:1924344 PMID:19913029 PMID:20164459 PMID:20525296 PMID:20555336 PMID:20591486 PMID:21077204 PMID:21094163 PMID:21174529 PMID:21217109 PMID:21219898 PMID:21352497 PMID:21357407 PMID:21922596 PMID:2215617 PMID:22164218 PMID:22995991 PMID:24265693 PMID:24520188 PMID:24760071 PMID:24935155 PMID:2509724 PMID:25097241 PMID:25101269 PMID:25221422 PMID:25525159 PMID:25741868 PMID:25999674 PMID:28041643 PMID:28492532 PMID:28559085 PMID:28981474 PMID:29068140 PMID:29099798 PMID:29847639 PMID:30240733 PMID:30718709 PMID:30977563 PMID:31100078 PMID:33576794 PMID:7981701 PMID:7987326 PMID:8088850 PMID:8240107 PMID:8253795 PMID:8317502 PMID:8328469 PMID:8353500 PMID:8401533 PMID:8554077 PMID:8841304 PMID:8905849 PMID:9050844 PMID:9197578 PMID:9380676 PMID:9483582 PMID:9536098 PMID:9618546


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant/Recessive | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:10521250 PMID:10967073 PMID:11094174 PMID:11139241 PMID:11141431 PMID:12660238 PMID:12860986 PMID:12871954 PMID:12966518 PMID:1301135 PMID:1303237 PMID:1484692 PMID:14971589 PMID:1580841 PMID:16123440 PMID:16767206 PMID:17014888 PMID:17488458 PMID:17576681 PMID:1765377 PMID:1783387 PMID:18175313 PMID:1833777 PMID:1840561 PMID:1862076 PMID:1882937 PMID:1897520 PMID:1924344 PMID:19913029 PMID:20164459 PMID:20525296 PMID:20555336 PMID:20591486 PMID:21077204 PMID:21094163 PMID:21174529 PMID:21217109 PMID:21219898 PMID:21352497 PMID:21357407 PMID:21922596 PMID:2215617 PMID:22164218 PMID:22995991 PMID:23591405 PMID:24265693 PMID:24520188 PMID:24760071 PMID:24935155 PMID:24938718 PMID:2509724 PMID:25097241 PMID:25101269 PMID:25221422 PMID:25408095 PMID:25525159 PMID:25741868 PMID:25999674 PMID:26962691 PMID:28041643 PMID:28076437 PMID:28492532 PMID:28524165 PMID:28559085 PMID:28981474 PMID:29068140 PMID:29099798 PMID:29847639 PMID:29890221 PMID:30240733 PMID:30718709 PMID:30977563 PMID:31100078 PMID:31908405 PMID:33576794 PMID:7724183 PMID:7981701 PMID:7987326 PMID:7987331 PMID:8045708 PMID:8088850 PMID:8240107 PMID:8253795 PMID:8317502 PMID:8328469 PMID:8353500 PMID:8401533 PMID:8406457 PMID:8554077 PMID:8841304 PMID:8905849 PMID:9050844 PMID:9197578 PMID:9380676 PMID:9483582 PMID:9536098 PMID:9618546


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant retinitis pigmentosa | ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant/Recessive | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:10521250 PMID:10967073 PMID:11094174 PMID:11139241 PMID:11141431 PMID:12660238 PMID:12860986 PMID:12871954 PMID:12966518 PMID:1301135 PMID:1303237 PMID:1484692 PMID:14971589 PMID:15126168 PMID:1580841 PMID:16123440 PMID:16737970 PMID:16767206 PMID:16799052 PMID:17014888 PMID:17488458 PMID:17576681 PMID:1765377 PMID:1783387 PMID:18175313 PMID:1833777 PMID:1840561 PMID:1862076 PMID:1882937 PMID:1897520 PMID:19085385 PMID:1924344 PMID:19913029 PMID:19960070 PMID:20164459 PMID:20525296 PMID:20555336 PMID:20591486 PMID:21077204 PMID:21094163 PMID:21174529 PMID:21217109 PMID:21219898 PMID:21352497 PMID:21357407 PMID:21922596 PMID:2215617 PMID:22164218 PMID:22252712 PMID:22791210 PMID:22968130 PMID:22995991 PMID:23221340 PMID:23591405 PMID:23625926 PMID:24106275 PMID:24265693 PMID:24520188 PMID:24760071 PMID:24935155 PMID:24938718 PMID:2509724 PMID:25097241 PMID:25101269 PMID:25221422 PMID:25408095 PMID:25525159 PMID:25741868 PMID:25999674 PMID:26887858 PMID:26962691 PMID:28041643 PMID:28076437 PMID:28341476 PMID:28492532 PMID:28524165 PMID:28559085 PMID:28981474 PMID:29068140 PMID:29099798 PMID:29847639 PMID:29890221 PMID:30240733 PMID:30718709 PMID:30977563 PMID:31100078 PMID:31319082 PMID:31456290 PMID:31908405 PMID:32037395 PMID:32581362 PMID:33576794 PMID:34906470 PMID:36909829 PMID:7724183 PMID:7981701 PMID:7987326 PMID:7987331 PMID:7987385 PMID:8045708 PMID:8088850 PMID:8240107 PMID:8253795 PMID:8317502 PMID:8328469 PMID:8353500 PMID:8401533 PMID:8406457 PMID:8554077 PMID:8841304 PMID:8905849 PMID:9050844 PMID:9197578 PMID:9380676 PMID:9483582 PMID:9536098 PMID:9618546 PMID:9810568


    • An association has been curated linking Rho and retinitis pigmentosa in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with RHO (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 600 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 36 papers in RGD have been used to annotate Rho
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant retinitis pigmentosa | ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant/Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:10521250 PMID:10967073 PMID:11094174 PMID:11139241 PMID:11141431 PMID:12660238 PMID:12860986 PMID:12871954 PMID:12966518 PMID:1301135 PMID:1303237 PMID:1484692 PMID:14971589 PMID:15126168 PMID:1580841 PMID:16123440 PMID:16737970 PMID:16799052 PMID:17014888 PMID:17488458 PMID:17576681 PMID:1765377 PMID:1783387 PMID:18175313 PMID:18310263 PMID:1833777 PMID:1840561 PMID:1862076 PMID:1882937 PMID:1897520 PMID:19085385 PMID:1924344 PMID:19913029 PMID:19960070 PMID:20164459 PMID:20525296 PMID:20555336 PMID:20591486 PMID:21077204 PMID:21094163 PMID:21174529 PMID:21217109 PMID:21219898 PMID:21352497 PMID:21357407 PMID:21922596 PMID:2215617 PMID:22164218 PMID:22252712 PMID:22791210 PMID:22968130 PMID:22995991 PMID:23221340 PMID:23591405 PMID:23625926 PMID:24106275 PMID:24265693 PMID:24520188 PMID:24760071 PMID:24935155 PMID:24938718 PMID:2509724 PMID:25097241 PMID:25101269 PMID:25221422 PMID:25408095 PMID:25525159 PMID:25741868 PMID:25999674 PMID:26887858 PMID:26962691 PMID:28041643 PMID:28076437 PMID:28341476 PMID:28492532 PMID:28524165 PMID:28559085 PMID:28981474 PMID:29068140 PMID:29099798 PMID:29847639 PMID:29890221 PMID:30240733 PMID:30718709 PMID:30977563 PMID:31100078 PMID:31319082 PMID:31456290 PMID:31908405 PMID:32037395 PMID:32581362 PMID:33576794 PMID:34906470 PMID:36909829 PMID:7724183 PMID:7981701 PMID:7987326 PMID:7987331 PMID:7987385 PMID:8045708 PMID:8088850 PMID:8240107 PMID:8253795 PMID:8317502 PMID:8328469 PMID:8353500 PMID:8401533 PMID:8406457 PMID:8554077 PMID:8841304 PMID:8905849 PMID:9050844 PMID:9197578 PMID:9380676 PMID:9483582 PMID:9536098 PMID:9618546 PMID:9810568


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