-
1
-
-
79960455119
-
A role for noncanonical microRNAs in the mammalian brain revealed by phenotypic differences in Dgcr8 versus Dicer1 knockouts and small RNA sequencing
-
Babiarz, J. E., Hsu, R., Melton, C., Thomas, M., Ullian, E. M., and Blelloch, R. (2011). A role for noncanonical microRNAs in the mammalian brain revealed by phenotypic differences in Dgcr8 versus Dicer1 knockouts and small RNA sequencing. RNA 17, 1489-1501.
-
(2011)
RNA
, vol.17
, pp. 1489-1501
-
-
Babiarz, J.E.1
Hsu, R.2
Melton, C.3
Thomas, M.4
Ullian, E.M.5
Blelloch, R.6
-
2
-
-
54349104464
-
Mouse ES cells express endogenous shRNAs, siRNAs, and other Microprocessor-independent, Dicer-dependent small RNAs
-
Babiarz, J. E., Ruby, J. G., Wang, Y., Bartel, D. P., and Blelloch, R. (2008). Mouse ES cells express endogenous shRNAs, siRNAs, and other Microprocessor-independent, Dicer-dependent small RNAs. Genes Dev. 22, 2773-2785.
-
(2008)
Genes Dev
, vol.22
, pp. 2773-2785
-
-
Babiarz, J.E.1
Ruby, J.G.2
Wang, Y.3
Bartel, D.P.4
Blelloch, R.5
-
3
-
-
84863116288
-
Ferric, not ferrous, heme activates RNA-binding protein DGCR8 for primary microRNA processing
-
Barr, I., Smith, A. T., Chen, Y., Senturia, R.,Burstyn,J.N.,andGuo,F. (2012). Ferric, not ferrous, heme activates RNA-binding protein DGCR8 for primary microRNA processing. Proc. Natl. Acad. Sci. U.S.A. 109, 1919-1924.
-
(2012)
Proc. Natl. Acad. Sci. U. S. A.
, vol.109
, pp. 1919-1924
-
-
Barr, I.1
Smith, A.T.2
Chen, Y.3
Senturia, R.4
Burstyn, J.N.5
Guo, F.6
-
4
-
-
33846446440
-
Accumulating quan- titative trait linkage evidence across multiple datasets using the posterior probability of linkage
-
Bartlett, C. W., and Vieland, V. J. (2007). Accumulating quan- titative trait linkage evidence across multiple datasets using the posterior probability of linkage. Genet. Epidemiol. 31, 91-102.
-
(2007)
Genet. Epidemiol.
, vol.31
, pp. 91-102
-
-
Bartlett, C.W.1
Vieland, V.J.2
-
5
-
-
34247636739
-
Catechol-O-methyl trans- ferase and expression of schizophre- nia in 73 adults with 22q11 dele- tion syndrome
-
Bassett, A. S., Caluseriu, O., Weksberg, R.,Young,D.A.,andChow,E.W. (2007). Catechol-O-methyl trans- ferase and expression of schizophre- nia in 73 adults with 22q11 dele- tion syndrome. Biol. Psychiatry 61, 1135-1140.
-
(2007)
Biol. Psychiatry
, vol.61
, pp. 1135-1140
-
-
Bassett, A.S.1
Caluseriu, O.2
Weksberg, R.3
Young, D.A.4
Chow, E.W.5
-
6
-
-
49649124127
-
Schizophrenia and 22q11. 2 deletion syndrome
-
Bassett, A. S., and Chow, E. W. (2008). Schizophrenia and 22q11.2 deletion syndrome. Curr.PsychiatryRep.10, 148-157.
-
(2008)
Curr. PsychiatryRep.
, vol.10
, pp. 148-157
-
-
Bassett, A.S.1
Chow, E.W.2
-
7
-
-
79960444931
-
Practical guidelines for managing patients with 22q11
-
Bassett, A. S., McDonald-McGinn, D. M., Devriendt, K., Digilio, M. C., Goldenberg, P., Habel, A., et al. (2011). Practical guidelines for managing patients with 22q11.2 deletion syndrome. J. Pediatr. 159, 332-339 e331.
-
(2011)
2 deletion syndrome. J. Pediatr.
, vol.159
, pp. 332-339
-
-
Bassett, A.S.1
McDonald-McGinn, D.M.2
Devriendt, K.3
Digilio, M.C.4
Goldenberg, P.5
Habel, A.6
-
8
-
-
84859500144
-
MicroRNA dysregulation in schizophrenia
-
Beveridge, N. J., and Cairns, M. J. (2012). MicroRNA dysregulation in schizophrenia. Neurobiol. Dis. 46, 263-271.
-
(2012)
Neurobiol. Dis.
, vol.46
, pp. 263-271
-
-
Beveridge, N.J.1
Cairns, M.J.2
-
9
-
-
0141617475
-
The risk of human immun- odeficiency virus-1 infection in twin pairs born to infected mothers in Africa
-
Biggar, R. J., Cassol, S., Kumwenda, N., Lema, V., Janes, M., Pilon, R., et al. (2003). The risk of human immun- odeficiency virus-1 infection in twin pairs born to infected mothers in Africa. J. Infect. Dis. 188, 850-855.
-
(2003)
J. Infect. Dis.
, vol.188
, pp. 850-855
-
-
Biggar, R.J.1
Cassol, S.2
Kumwenda, N.3
Lema, V.4
Janes, M.5
Pilon, R.6
-
10
-
-
67749132423
-
Argonaute HITS-CLIP decodes microRNA- mRNA interaction maps
-
Chi, S. W., Zang, J. B., Mele, A., and Darnell, R. B. (2009). Argonaute HITS-CLIP decodes microRNA- mRNA interaction maps. Nature 460, 479-486.
-
(2009)
Nature
, vol.460
, pp. 479-486
-
-
Chi, S.W.1
Zang, J.B.2
Mele, A.3
Darnell, R.B.4
-
11
-
-
0027370619
-
Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis
-
Driscoll, D. A., Salvin, J., Sellinger, B., Budarf, M. L., McDonald-McGinn, D. M., Zackai, E. H., et al. (1993). Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis. J. Med. Genet. 30, 813-817.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 813-817
-
-
Driscoll, D.A.1
Salvin, J.2
Sellinger, B.3
Budarf, M.L.4
McDonald-McGinn, D.M.5
Zackai, E.H.6
-
12
-
-
79959805164
-
miRWalk- database: prediction of possible miRNA binding sites by "walk- ing" the genes of three genomes
-
Dweep, H., Sticht, C., Pandey, P., and Gretz, N. (2011). miRWalk- database: prediction of possible miRNA binding sites by "walk- ing" the genes of three genomes. J. Biomed. Inform. 44, 839-847.
-
(2011)
J. Biomed. Inform.
, vol.44
, pp. 839-847
-
-
Dweep, H.1
Sticht, C.2
Pandey, P.3
Gretz, N.4
-
13
-
-
0033358588
-
Low-copy repeats mediate the common 3- Mb deletion in patients with velo- cardio-facial syndrome
-
Edelmann, L., Pandita, R. K., and Morrow, B. E. (1999). Low-copy repeats mediate the common 3- Mb deletion in patients with velo- cardio-facial syndrome. Am. J. Hum. Genet. 64, 1076-1086.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1076-1086
-
-
Edelmann, L.1
Pandita, R.K.2
Morrow, B.E.3
-
14
-
-
78651320424
-
The UCSC Genome Browser database: update 2011
-
Fujita, P. A., Rhead, B., Zweig, A. S., Hinrichs, A. S., Karolchik, D., Cline, M. S., et al. (2011). The UCSC Genome Browser database: update 2011. Nucleic Acids Res. 39, D876-D882.
-
(2011)
Nucleic Acids Res
, vol.39
-
-
Fujita, P.A.1
Rhead, B.2
Zweig, A.S.3
Hinrichs, A.S.4
Karolchik, D.5
Cline, M.S.6
-
15
-
-
77955401776
-
Elevated preva- lence of generalized anxiety disorder in adults with 22q11.2 deletion syn- drome
-
Fung,W.L.,McEvilly,R.,Fong,J., Silversides, C., Chow, E., and Bassett, A. (2010). Elevated preva- lence of generalized anxiety disorder in adults with 22q11.2 deletion syn- drome. Am. J. Psychiatry 167, 998.
-
(2010)
Am. J. Psychiatry
, vol.167
, pp. 998
-
-
Fung, W.L.1
McEvilly, R.2
Fong, J.3
Silversides, C.4
Chow, E.5
Bassett, A.6
-
16
-
-
0031671548
-
A population study of chromosome 22q11 dele- tions in infancy
-
Goodship, J., Cross, I., Liling, J., and Wren, C. (1998). A population study of chromosome 22q11 dele- tions in infancy. Arch. Dis. Child. 79, 348-351.
-
(1998)
Arch. Dis. Child.
, vol.79
, pp. 348-351
-
-
Goodship, J.1
Cross, I.2
Liling, J.3
Wren, C.4
-
17
-
-
80054695658
-
Genotype and cardiovascular phenotype correlations with TBX1 in 1. 022 velo-cardio- facial/DiGeorge/22q11. 2 deletion syndrome patients
-
Guo, T., McDonald-McGinn, D., Blonska, A., Shanske, A., Bassett, A. S., Chow, E., et al. (2011). Genotype and cardiovascular phenotype correlations with TBX1 in 1, 022 velo-cardio- facial/DiGeorge/22q11.2 deletion syndrome patients. Hum. Mutat. 32, 1278-1289.
-
(2011)
Hum. Mutat.
, vol.32
, pp. 1278-1289
-
-
Guo, T.1
McDonald-McGinn, D.2
Blonska, A.3
Shanske, A.4
Bassett, A.S.5
Chow, E.6
-
18
-
-
77950920903
-
Transcriptome-wide identifica- tion of RNA-binding protein and microRNA target sites by PAR-CLIP
-
Hafner, M., Landthaler, M., Burger, L., Khorshid, M., Hausser, J., Berninger, P., et al. (2010). Transcriptome-wide identifica- tion of RNA-binding protein and microRNA target sites by PAR-CLIP. Cell 141, 129-141.
-
(2010)
Cell
, vol.141
, pp. 129-141
-
-
Hafner, M.1
Landthaler, M.2
Burger, L.3
Khorshid, M.4
Hausser, J.5
Berninger, P.6
-
19
-
-
84984765621
-
Canalization of development by microRNAs
-
Hornstein, E., and Shomron, N. (2006). Canalization of development by microRNAs. Nat. Genet. 38(Suppl.), S20-S24.
-
(2006)
Nat. Genet.
, vol.38
, Issue.SUPPL.
-
-
Hornstein, E.1
Shomron, N.2
-
20
-
-
0035089146
-
Comparison of 'model-free' and 'model-based' linkage statistics in the presence of locus heterogene- ity: single data set and multiple data set applications
-
Huang, J., and Vieland, V. J. (2001). Comparison of 'model-free' and 'model-based' linkage statistics in the presence of locus heterogene- ity: single data set and multiple data set applications. Hum. Hered. 51, 217-225.
-
(2001)
Hum. Hered.
, vol.51
, pp. 217-225
-
-
Huang, J.1
Vieland, V.J.2
-
21
-
-
38049002368
-
Exploiting gene x gene interaction in linkage analysis
-
Huang, Y., Bartlett, C. W., Segre, A. M., O'Connell, J. R., Mangin, L., and Vieland, V. J. (2007). Exploiting gene x gene interaction in linkage analysis. BMC Proc. 1(Suppl. 1):S64.
-
(2007)
BMC Proc
, vol.1
, Issue.SUPPL 1
-
-
Huang, Y.1
Bartlett, C.W.2
Segre, A.M.3
O'Connell, J.R.4
Mangin, L.5
Vieland, V.J.6
-
22
-
-
78649526217
-
Association statistics under the PPL framework
-
Huang, Y., and Vieland, V. J. (2010). Association statistics under the PPL framework. Genet. Epidemiol. 34, 835-845.
-
(2010)
Genet. Epidemiol.
, vol.34
, pp. 835-845
-
-
Huang, Y.1
Vieland, V.J.2
-
23
-
-
78149428430
-
Rethinking schizophrenia
-
Insel, T. R. (2010). Rethinking schizophrenia. Nature 468, 187-193.
-
(2010)
Nature
, vol.468
, pp. 187-193
-
-
Insel, T.R.1
-
24
-
-
0036079158
-
The human genome browser at UCSC
-
Kent,W.J.,Sugnet,C.W.,Furey,T.S., Roskin, K. M., Pringle, T. H., Zahler, A. M., et al. (2002). The human genome browser at UCSC. Genome Res. 12, 996-1006.
-
(2002)
Genome Res
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
Sugnet, C.W.2
Furey, T.S.3
Roskin, K.M.4
Pringle, T.H.5
Zahler, A.M.6
-
25
-
-
84865985475
-
Experimental validation of candi- date schizophrenia gene ZNF804A as target for hsa-miR-137
-
Kim,A.H.,Parker,E.K.,Williamson, V.,McMichael,G.O.,Fanous,A. H., and Vladimirov, V. I. (2012). Experimental validation of candi- date schizophrenia gene ZNF804A as target for hsa-miR-137. Schizophr. Res. 141, 60-64.
-
(2012)
Schizophr. Res.
, vol.141
, pp. 60-64
-
-
Kim, A.H.1
Parker, E.K.2
Williamson, V.3
McMichael, G.O.4
Fanous, A.H.5
Vladimirov, V.I.6
-
26
-
-
70349611559
-
Cis-ruption mechanisms: disruption of cis-regulatory control as a cause of human genetic disease
-
Kleinjan, D.-J., and Coutinho, P. (2009). Cis-ruption mechanisms: disruption of cis-regulatory control as a cause of human genetic disease. Brief. Funct. Genomic. Proteomic. 8, 317-332.
-
(2009)
Brief. Funct. Genomic. Proteomic.
, vol.8
, pp. 317-332
-
-
Kleinjan, D.-J.1
Coutinho, P.2
-
27
-
-
68049120574
-
Disorders of the genome architecture: a review
-
Kumar, D. (2008). Disorders of the genome architecture: a review. Genomic. Med. 2, 69-76.
-
(2008)
Genomic. Med.
, vol.2
, pp. 69-76
-
-
Kumar, D.1
-
28
-
-
84871270974
-
Validation of schizophrenia- associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR- 137 targets
-
[Epub ahead of print] doi: 10. 1038/mp. 2011. 170
-
Kwon, E., Wang, W., and Tsai, L. H. (2011). Validation of schizophrenia- associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR- 137 targets. Mol. Psychiatry.doi: 10.1038/mp.2011.170. [Epub ahead of print].
-
(2011)
Mol. Psychiatry.
-
-
Kwon, E.1
Wang, W.2
Tsai, L.H.3
-
29
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander, E. S., Linton, L. M., Birren, B.,Nusbaum,C.,Zody,M.C., Baldwin, J., et al. (2001). Initial sequencing and analysis of the human genome. Nature 409, 860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
-
30
-
-
33645049865
-
Genetic variables that influence phenotype
-
Linder, C. C. (2006). Genetic variables that influence phenotype. ILAR J. 47, 132-140.
-
(2006)
ILAR J
, vol.47
, pp. 132-140
-
-
Linder, C.C.1
-
31
-
-
30344485473
-
Performance comparison of two- point linkage methods using microsatellite markers flanking known disease locations
-
doi: 10.1186/1471-2156-6-S1-S141
-
Logue, M. W., George, A. W., Spence, M. A., and Vieland, V. J. (2005). Performance comparison of two- point linkage methods using microsatellite markers flanking known disease locations. BMC Genet. 6(Suppl. 1):S141. doi: 10.1186/1471-2156-6-S1-S141
-
(2005)
BMC Genet
, vol.6
, Issue.SUPPL 1
-
-
Logue, M.W.1
George, A.W.2
Spence, M.A.3
Vieland, V.J.4
-
32
-
-
79953312246
-
Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain devel- opment: patterning, proliferation, and mitochondrial functions of 22q11 genes
-
Meechan, D. W., Maynard, T. M., Tucker, E. S., and Lamantia, A. S. (2011). Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain devel- opment: patterning, proliferation, and mitochondrial functions of 22q11 genes. Int. J. Dev. Neurosci. 29, 283-294.
-
(2011)
Int. J. Dev. Neurosci.
, vol.29
, pp. 283-294
-
-
Meechan, D.W.1
Maynard, T.M.2
Tucker, E.S.3
Lamantia, A.S.4
-
33
-
-
84866866864
-
The emerging role of microRNAs in schizophrenia and autism spectrum disorders
-
doi: 10.3389/fpsyt.2012.00039
-
Mellios, N., and Sur, M. (2012). The emerging role of microRNAs in schizophrenia and autism spectrum disorders. Front Psychiatry 3:39. doi: 10.3389/fpsyt.2012.00039
-
(2012)
Front Psychiatry
, vol.3
, pp. 39
-
-
Mellios, N.1
Sur, M.2
-
34
-
-
78650446774
-
Altered microRNA expression profiles in postmortem brain samples from individuals with schizophrenia and bipolar disorder
-
Moreau, M. P., Bruse, S. E., David-Rus, R., Buyske, S., and Brzustowicz, L. M. (2011). Altered microRNA expression profiles in postmortem brain samples from individuals with schizophrenia and bipolar disorder. Biol. Psychiatry 69, 188-193.
-
(2011)
Biol. Psychiatry
, vol.69
, pp. 188-193
-
-
Moreau, M.P.1
Bruse, S.E.2
David-Rus, R.3
Buyske, S.4
Brzustowicz, L.M.5
-
35
-
-
80053384370
-
Genome-wide association study identifies five new schizophrenia loci
-
Ripke, S., Sanders, A. R., Kendler, K. S., Levinson, D. F., Sklar, P., Holmans, P. A., et al. (2011). Genome-wide association study identifies five new schizophrenia loci. Nat. Genet. 43, 969-976.
-
(2011)
Nat. Genet.
, vol.43
, pp. 969-976
-
-
Ripke, S.1
Sanders, A.R.2
Kendler, K.S.3
Levinson, D.F.4
Sklar, P.5
Holmans, P.A.6
-
37
-
-
84875420225
-
MicroRNAs in cancers and neu- rodegenerative disorders
-
doi: 10.3389/ fgene.2012.00194
-
Saito, Y., and Saito, H. (2012). MicroRNAs in cancers and neu- rodegenerative disorders. Front. Gene. 3:194. doi: 10.3389/ fgene.2012.00194
-
(2012)
Front. Gene.
, vol.3
, pp. 194
-
-
Saito, Y.1
Saito, H.2
-
38
-
-
0034161932
-
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
-
Shaikh, T. H., Kurahashi, H., Saitta, S. C., O'Hare, A. M., Hu, P., Roe, B. A., et al. (2000). Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis. Hum. Mol. Genet. 9, 489-501.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 489-501
-
-
Shaikh, T.H.1
Kurahashi, H.2
Saitta, S.C.3
O'Hare, A.M.4
Hu, P.5
Roe, B.A.6
-
39
-
-
43949124669
-
Altered brain microRNA biogenesis contributes to pheno- typic deficits in a 22q11-deletion mouse model
-
Stark, K. L., Xu, B., Bagchi, A., Lai, W.-S., Liu, H., Hsu, R., et al. (2008). Altered brain microRNA biogenesis contributes to pheno- typic deficits in a 22q11-deletion mouse model. Nat. Genet. 40, 751-760.
-
(2008)
Nat. Genet.
, vol.40
, pp. 751-760
-
-
Stark, K.L.1
Xu, B.2
Bagchi, A.3
Lai, W.-S.4
Liu, H.5
Hsu, R.6
-
40
-
-
33748591490
-
Thermometers: something for statistical geneticists to think about
-
Vieland, V. J. (2006). Thermometers: something for statistical geneticists to think about. Hum. Hered. 61, 144-156.
-
(2006)
Hum. Hered.
, vol.61
, pp. 144-156
-
-
Vieland, V.J.1
-
41
-
-
79958065866
-
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism
-
Vieland, V. J., Hallmayer, J., Huang, Y., Pagnamenta, A. T., Pinto, D., Khan, H., et al. (2011a). Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. J. Neurodev. Disord. 3, 113-123.
-
(2011)
J. Neurodev. Disord.
, vol.3
, pp. 113-123
-
-
Vieland, V.J.1
Hallmayer, J.2
Huang, Y.3
Pagnamenta, A.T.4
Pinto, D.5
Khan, H.6
-
42
-
-
0002985658
-
Reveiw of statistical evidence: a likelihood paradigm
-
Vieland, V. J., and Hodge, S. E. (1998). Reveiw of statistical evidence: a likelihood paradigm. Am. J. Hum. Genet. 63, 283-289.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 283-289
-
-
Vieland, V.J.1
Hodge, S.E.2
-
43
-
-
84055184748
-
KELVIN: a software package for rigorous measurement of statistical evidence in human genetics
-
Vieland, V. J., Huang, Y., Seok, S. C., Burian, J., Catalyurek, U., O'Connell, J., et al. (2011b). KELVIN: a software package for rigorous measurement of statistical evidence in human genetics. Hum. Hered. 72, 276-288.
-
(2011)
Hum. Hered.
, vol.72
, pp. 276-288
-
-
Vieland, V.J.1
Huang, Y.2
Seok, S.C.3
Burian, J.4
Catalyurek, U.5
O'Connell, J.6
-
44
-
-
0035089255
-
Power to detect link- age based on multiple sets of data in the presence of locus heterogeneity: comparative evaluation of model-based linkage methods for affected sib pair data
-
Vieland, V. J., Wang, K., and Huang, J. (2001). Power to detect link- age based on multiple sets of data in the presence of locus heterogeneity: comparative evaluation of model-based linkage methods for affected sib pair data. Hum. Hered. 51, 199-208.
-
(2001)
Hum. Hered.
, vol.51
, pp. 199-208
-
-
Vieland, V.J.1
Wang, K.2
Huang, J.3
-
45
-
-
63449086286
-
Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome
-
Vorstman,J.A.,Chow,E.W.,Ophoff, R. A., Van Engeland, H., Beemer, F. A., Kahn, R. S., et al. (2009). Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome. Am. J. Med. Genet. B Neuropsychiatr. Genet. 150B, 430-433.
-
(2009)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.150 B
, pp. 430-433
-
-
Vorstman, J.A.1
Chow, E.W.2
Ophoff, R.A.3
Van Engeland, H.4
Beemer, F.A.5
Kahn, R.S.6
-
46
-
-
46249093584
-
Strong association of de novo copy num- ber mutations with sporadic schizophrenia
-
Xu, B., Roos, J. L., Levy, S., Van Rensburg,E.J.,Gogos,J.A.,and Karayiorgou, M. (2008). Strong association of de novo copy num- ber mutations with sporadic schizophrenia. Nat. Genet. 40, 880-885.
-
(2008)
Nat. Genet.
, vol.40
, pp. 880-885
-
-
Xu, B.1
Roos, J.L.2
Levy, S.3
Van Rensburg, E.J.4
Gogos, J.A.5
Karayiorgou, M.6
-
47
-
-
78651307694
-
starBase: a database for exploring microRNA-mRNA inter- action maps from Argonaute CLIP-Seq and Degradome- Seq data
-
Yang, J. H., Li, J. H., Shao, P., Zhou, H.,Chen,Y.Q.,andQu,L.H. (2011). starBase: a database for exploring microRNA-mRNA inter- action maps from Argonaute CLIP-Seq and Degradome- Seq data. Nucleic Acids Res. 39, D202-D209.
-
(2011)
Nucleic Acids Res
, vol.39
-
-
Yang, J.H.1
Li, J.H.2
Shao, P.3
Zhou, H.4
Chen, Y.Q.5
Qu, L.H.6
-
48
-
-
84862134570
-
Systematic association analysis of microRNA machinery genes with schizophrenia informs fur- ther study
-
Zhang,F.,Chen,Y.,Liu,C.,Lu,T., Yan, H., Ruan, Y., et al. (2012). Systematic association analysis of microRNA machinery genes with schizophrenia informs fur- ther study. Neurosci. Lett. 520, 47-50.
-
(2012)
Neurosci. Lett.
, vol.520
, pp. 47-50
-
-
Zhang, F.1
Chen, Y.2
Liu, C.3
Lu, T.4
Yan, H.5
Ruan, Y.6
-
49
-
-
76349122201
-
Comprehensive discov- ery of endogenous Argonaute binding sites in Caenorhabditis elegans
-
Zisoulis, D. G., Lovci, M. T., Wilbert, M.L.,Hutt,K.R.,Liang,T. Y., Pasquinelli, A. E., et al. (2010). Comprehensive discov- ery of endogenous Argonaute binding sites in Caenorhabditis elegans. Nat. Struct. Mol. Biol. 17, 173-179.
-
(2010)
Nat. Struct. Mol. Biol.
, vol.17
, pp. 173-179
-
-
Zisoulis, D.G.1
Lovci, M.T.2
Wilbert, M.L.3
Hutt, K.R.4
Liang, T.Y.5
Pasquinelli, A.E.6
|