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“Coexpression of interleukin-6 and -2 from giant panda in Escherichia coli and the biological activity of the fusion protein”, vol. 12, pp. 1987-1995, 2013.
, “Mitotic and meiotic behavior of rye chromosomes in wheat - Psathyrostachys huashanica amphiploid x triticale progeny”, vol. 12, pp. 2537-2548, 2013.
, , “Microdeletion on 17p11.2 in a Smith-Magenis syndrome patient with mental retardation and congenital heart defect: first report from China”, vol. 11, pp. 2321-2327, 2012.
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Cassidy SB and Driscoll DJ (2009). Prader-Willi syndrome. Eur. J. Hum. Genet. 17: 3-13.
http://dx.doi.org/10.1038/ejhg.2008.165
PMid:18781185 PMCid:2985966
Chen JL, Yang YF, Huang C, Wang J, et al. (2012). Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies. Am. J. Med. Genet. A 158A: 685-688.
http://dx.doi.org/10.1002/ajmg.a.34434
PMid:22307725
Edelman EA, Girirajan S, Finucane B, Patel PI, et al. (2007). Gender, genotype, and phenotype differences in Smith- Magenis syndrome: a meta-analysis of 105 cases. Clin. Genet. 71: 540-550.
http://dx.doi.org/10.1111/j.1399-0004.2007.00815.x
PMid:17539903
Elsea SH and Girirajan S (2008). Smith-Magenis syndrome. Eur. J. Hum. Genet. 16: 412-421.
http://dx.doi.org/10.1038/sj.ejhg.5202009
PMid:18231123
Engelstad H, Carney G, S'aulis D, Rise J, et al. (2011). Large contiguous gene deletions in Sjogren-Larsson syndrome. Mol. Genet. Metab. 104: 356-361.
http://dx.doi.org/10.1016/j.ymgme.2011.05.015
PMid:21684788 PMCid:3196763
Gamba BF, Vieira GH, Souza DH, Monteiro FF, et al. (2011). Smith-Magenis syndrome: clinical evaluation in seven Brazilian patients. Genet. Mol. Res. 10: 2664-2670.
http://dx.doi.org/10.4238/2011.October.31.17
PMid:22057962
Girirajan S, Elsas LJ, Devriendt K and Elsea SH (2005). RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions. J. Med. Genet. 42: 820-828.
http://dx.doi.org/10.1136/jmg.2005.031211
PMid:15788730 PMCid:1735950
Girirajan S, Vlangos CN, Szomju BB, Edelman E, et al. (2006). Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum. Genet. Med. 8: 417-427.
http://dx.doi.org/10.1097/01.gim.0000228215.32110.89
PMid:16845274
Greenberg F, Guzzetta V, Montes dO-L, Magenis RE, et al. (1991). Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2). Am. J. Hum. Genet. 49: 1207-1218.
PMid:1746552 PMCid:1686451
Greenberg F, Lewis RA, Potocki L, Glaze D, et al. (1996). Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2). Am. J. Med. Genet. 62: 247-254.
http://dx.doi.org/10.1002/(SICI)1096-8628(19960329)62:3<247::AID-AJMG9>3.0.CO;2-Q
Gropman AL, Duncan WC and Smith AC (2006). Neurologic and developmental features of the Smith-Magenis syndrome (del 17p11.2). Pediatr. Neurol. 34: 337-350.
http://dx.doi.org/10.1016/j.pediatrneurol.2005.08.018
PMid:16647992
Huang C, Yang YF, Yin N, Chen JL, et al. (2012). Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion. Gene 498: 308-310.
http://dx.doi.org/10.1016/j.gene.2012.01.083
PMid:22366306
Kalay E, Uzumcu A, Krieger E, Caylan R, et al. (2007). MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation. Am. J. Med. Genet. A 143A: 2382-2389.
http://dx.doi.org/10.1002/ajmg.a.31937
PMid:17853461
Kleefstra T, van Zelst-Stams WA, Nillesen WM, Cormier-Daire V, et al. (2009). Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. J. Med. Genet. 46: 598-606.
http://dx.doi.org/10.1136/jmg.2008.062950
PMid:19264732
Kobrynski LJ and Sullivan KE (2007). Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes. Lancet 370: 1443-1452.
http://dx.doi.org/10.1016/S0140-6736(07)61601-8
Myers SM and Challman TD (2004). Congenital heart defects associated with Smith-Magenis syndrome: two cases of total anomalous pulmonary venous return. Am. J. Med. Genet. A 131: 99-100.
http://dx.doi.org/10.1002/ajmg.a.30290
PMid:15384100
Neumann SA, Tingley WG, Conklin BR, Shrader CJ, et al. (2009). AKAP10 (I646V) functional polymorphism predicts heart rate and heart rate variability in apparently healthy, middle-aged European-Americans. Psychophysiology 46: 466-472.
http://dx.doi.org/10.1111/j.1469-8986.2009.00802.x
PMid:19496216 PMCid:2890278
Shi FD and Jia JP (2011). Neurology and neurologic practice in China. Neurology 77: 1986-1992.
http://dx.doi.org/10.1212/WNL.0b013e31823a0ed3
PMid:22123780
Slager RE, Newton TL, Vlangos CN, Finucane B, et al. (2003). Mutations in RAI1 associated with Smith-Magenis syndrome. Nat. Genet. 33: 466-468.
http://dx.doi.org/10.1038/ng1126
PMid:12652298
Slavotinek AM (2008). Novel microdeletion syndromes detected by chromosome microarrays. Hum. Genet. 124: 1-17.
http://dx.doi.org/10.1007/s00439-008-0513-9
PMid:18512078
Smith AC, McGavran L, Waldstein G and Robinson J (1982). Deletion of the 17 short arm in two patients with facial clefts. Am. J. Hum. Genet. 34 (Suppl): 410A.
Smith AC, McGavran L, Robinson J, Waldstein G, et al. (1986). Interstitial deletion of (17)(p11.2p11.2) in nine patients. Am. J. Med. Genet. 24: 393-414.
http://dx.doi.org/10.1002/ajmg.1320240303
PMid:2425619
Stratton RF, Dobyns WB, Greenberg F, DeSana JB, et al. (1986). Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome. Am. J. Med. Genet. 24: 421-432.
http://dx.doi.org/10.1002/ajmg.1320240305
PMid:3728561
Sweeney E, Peart I, Tofeig M and Kerr B (1999). Smith-Magenis syndrome and tetralogy of Fallot. J. Med. Genet. 36: 501-502.
PMid:10874646 PMCid:1734392
Tan ZP, Huang C, Xu ZB, Yang JF, et al. (2011). Novel ZFPM2/FOG2 variants in patients with double outlet right ventricle. Clin. Genet. DOI 10.1111/j.1399-0004.2011.01787.x.
http://dx.doi.org/10.1111/j.1399-0004.2011.01787.x
Wong JT, Chan DK, Wong KY, Tan M, et al. (2003). Smith-Magenis syndrome and cyanotic congenital heart disease: a case report. Clin. Dysmorphol. 12: 73-74.
http://dx.doi.org/10.1097/00019605-200301000-00014
PMid:12514371
“Novel nonsense and frameshift NTRK1 gene mutations in Chinese patients with congenital insensitivity to pain with anhidrosis”, vol. 11, pp. 2156-2162, 2012.
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Beigelman A, Levy J, Hadad N, Pinsk V, et al. (2009). Abnormal neutrophil chemotactic activity in children with congenital insensitivity to pain with anhidrosis (CIPA): the role of nerve growth factor. Clin. Immunol. 130: 365-372.
http://dx.doi.org/10.1016/j.clim.2008.09.005
PMid:18955016
Bodzioch M, Lapicka K, Aslanidis C, Kacinski M, et al. (2001). Two novel mutant alleles of the gene encoding neurotrophic tyrosine kinase receptor type 1 (NTRK1) in a patient with congenital insensitivity to pain with anhidrosis: a splice junction mutation in intron 5 and cluster of four mutations in exon 15. Hum. Mutat. 17: 72.
http://dx.doi.org/10.1002/1098-1004(2001)17:1<72::AID-HUMU10>3.0.CO;2-X
Bonkowsky JL, Johnson J, Carey JC, Smith AG, et al. (2003). An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis. Pediatrics 112: e237-e241.
http://dx.doi.org/10.1542/peds.112.3.e237
PMid:12949319
Greco A, Villa R, Fusetti L, Orlandi R, et al. (2000). The Gly571Arg mutation, associated with the autonomic and sensory disorder congenital insensitivity to pain with anhidrosis, causes the inactivation of the NTRK1/nerve growth factor receptor. J. Cell Physiol. 182: 127-133.
http://dx.doi.org/10.1002/(SICI)1097-4652(200001)182:1<127::AID-JCP14>3.0.CO;2-0
Guo YC, Liao KK, Soong BW, Tsai CP, et al. (2004). Congenital insensitivity to pain with anhidrosis in Taiwan: a morphometric and genetic study. Eur. Neurol. 51: 206-214.
http://dx.doi.org/10.1159/000078487
PMid:15159601
Huehne K, Zweier C, Raab K, Odent S, et al. (2008). Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis. Neuromuscul. Disord. 18: 159-166.
http://dx.doi.org/10.1016/j.nmd.2007.10.005
PMid:18077166
Indo Y (2001). Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor. Hum. Mutat. 18: 462-471.
http://dx.doi.org/10.1002/humu.1224
PMid:11748840
Indo Y, Tsuruta M, Hayashida Y, Karim MA, et al. (1996). Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis. Nat. Genet. 13: 485-488.
http://dx.doi.org/10.1038/ng0896-485
PMid:8696348
Indo Y, Mardy S, Miura Y, Moosa A, et al. (2001). Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency. Hum. Mutat. 18: 308-318.
http://dx.doi.org/10.1002/humu.1192
PMid:11668614
Kilic SS, Ozturk R, Sarisozen B, Rotthier A, et al. (2009). Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis. Neurogenetics 10: 161-165.
http://dx.doi.org/10.1007/s10048-008-0165-x
PMid:19089473
Lee ST, Lee J, Lee M, Kim JW, et al. (2009). Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis. Muscle Nerve 40: 855-859.
http://dx.doi.org/10.1002/mus.21340
PMid:19618435
Lin YP, Su YN, Weng WC and Lee WT (2010). Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosis. J. Child. Neurol. 25: 1548-1551.
http://dx.doi.org/10.1177/0883073810375464
PMid:20647579
Mardy S, Miura Y, Endo F, Matsuda I, et al. (1999). Congenital insensitivity to pain with anhidrosis: novel mutations in the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor. Am. J. Hum. Genet. 64: 1570- 1579.
http://dx.doi.org/10.1086/302422
PMid:10330344 PMCid:1377900
Mardy S, Miura Y, Endo F, Matsuda I, et al. (2001). Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor. Hum. Mol. Genet. 10: 179-188.
http://dx.doi.org/10.1093/hmg/10.3.179
PMid:11159935
Miranda C, Di VM, Selleri S, Zanotti G, et al. (2002). Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations. J. Biol. Chem. 277: 6455-6462.
http://dx.doi.org/10.1074/jbc.M110016200
PMid:11719521
Miura Y, Mardy S, Awaya Y, Nihei K, et al. (2000). Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families. Hum. Genet. 106: 116-124.
http://dx.doi.org/10.1007/s004390051018
PMid:10982191
Miura Y, Hiura M, Torigoe K, Numata O, et al. (2000). Complete paternal uniparental isodisomy for chromosome 1 revealed by mutation analyses of the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with congenital insensitivity to pain with anhidrosis. Hum. Genet. 107: 205-209.
http://dx.doi.org/10.1007/s004390000369
PMid:11071380
Rosemberg S, Marie SK and Kliemann S (1994). Congenital insensitivity to pain with anhidrosis (hereditary sensory and autonomic neuropathy type IV). Pediatr. Neurol. 11: 50-56.
http://dx.doi.org/10.1016/0887-8994(94)90091-4
Sato Y, Tsuboi Y, Kurosawa H, Sugita K, et al. (2004). Anti-apoptotic effect of nerve growth factor is lost in congenital insensitivity to pain with anhidrosis (CIPA) B lymphocytes. J. Clin. Immunol. 24: 302-308.
http://dx.doi.org/10.1023/B:JOCI.0000025452.79585.a1
PMid:15114061
Shatzky S, Moses S, Levy J, Pinsk V, et al. (2000). Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli- Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies. Am. J. Med. Genet. 92: 353-360.
http://dx.doi.org/10.1002/1096-8628(20000619)92:5<353::AID-AJMG12>3.0.CO;2-C
Suriu C, Khayat M, Weiler M, Kfir N, et al. (2009). Skoura - a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene. Clin. Genet. 75: 230-236.
http://dx.doi.org/10.1111/j.1399-0004.2008.01143.x
PMid:19250380
Swanson AG (1963). Congenital insensitivity to pain with anhidrosis. A unique syndrome in two male siblings. Arch. Neurol. 8: 299-306.
http://dx.doi.org/10.1001/archneur.1963.00460030083008
PMid:13979626
Vardy PA, Greenberg LW, Kachel C and de Leon GF (1979). Congenital insensitivity to pain with anhydrosis. Report of a family and review of literature with reference to immune deficiency. Am. J. Dis. Child. 133: 1153-1155.
PMid:92193
“Patterns of synonymous codon usage bias in the model grass Brachypodium distachyon”, vol. 11, pp. 4695-4706, 2012.
, Bulmer M (1988). Are codon usage patterns in unicellular organisms determined by selection-mutation balance? J. Mol. Biol. 1: 15-26.
Bulmer M (1991). The selection-mutation-drift theory of synonymous codon usage. Genetics 129: 897-907.
PMid:1752426 PMCid:1204756
Carels N and Bernardi G (2000). Two classes of genes in plants. Genetics 154: 1819-1825.
PMid:10747072 PMCid:1461008
Chiapello H, Lisacek F, Caboche M and Henaut A (1998). Codon usage and gene function are related in sequences of Arabidopsis thaliana. Gene 209: GC1-GC38.
http://dx.doi.org/10.1016/S0378-1119(97)00671-9
De Amicis F and Marchetti S (2000). Intercodon dinucleotides affect codon choice in plant genes. Nucleic Acids Res. 28: 3339-3345.
http://dx.doi.org/10.1093/nar/28.17.3339
PMid:10954603 PMCid:110687
Doust A (2007). Architectural evolution and its implications for domestication in grasses. Ann. Bot. 100: 941-950.
http://dx.doi.org/10.1093/aob/mcm040
PMid:17478546 PMCid:2759198
Draper J, Mur LA, Jenkins G, Ghosh-Biswas GC, et al. (2001). Brachypodium distachyon. A new model system for functional genomics in grasses. Plant Physiol. 127: 1539-1555.
http://dx.doi.org/10.1104/pp.010196
PMid:11743099 PMCid:133562
Duret L and Mouchiroud D (1999). Expression pattern and, surprisingly, gene length shape codon usage in Caenorhabditis, Drosophila, and Arabidopsis. Proc. Natl. Acad. Sci. U. S. A. 96: 4482-4487.
http://dx.doi.org/10.1073/pnas.96.8.4482
PMid:10200288 PMCid:16358
Eyre-Walker AC (1991). An analysis of codon usage in mammals: selection or mutation bias? J. Mol. Evol. 33: 442-449.
http://dx.doi.org/10.1007/BF02103136
PMid:1960741
Gupta SK, Bhattacharyya TK and Ghosh TC (2004). Synonymous codon usage in Lactococcus lactis: mutational bias versus translational selection. J. Biomol. Struct. Dyn. 21: 527-536.
http://dx.doi.org/10.1080/07391102.2004.10506946
PMid:14692797
Hershberg R and Petrov DA (2008). Selection on codon bias. Annu. Rev. Genet. 42: 287-299.
http://dx.doi.org/10.1146/annurev.genet.42.110807.091442
PMid:18983258
International Brachypodium Initiative (2010). Genome sequencing and analysis of the model grass Brachypodium distachyon. Nature 463: 763-768.
http://dx.doi.org/10.1038/nature08747
PMid:20148030
Jiang Y, Deng F, Wang H and Hu Z (2008). An extensive analysis on the global codon usage pattern of baculoviruses. Arch. Virol. 153: 2273-2282.
http://dx.doi.org/10.1007/s00705-008-0260-1
PMid:19030954
Kawabe A and Miyashita NT (2003). Patterns of codon usage bias in three dicot and four monocot plant species. Genes Genet. Syst. 78: 343-352.
http://dx.doi.org/10.1266/ggs.78.343
PMid:14676425
Liu H, He R, Zhang H, Huang Y, et al. (2010). Analysis of synonymous codon usage in Zea mays. Mol. Biol. Rep. 37: 677-684.
http://dx.doi.org/10.1007/s11033-009-9521-7
PMid:19330534
Liu Q (2006). Analysis of codon usage pattern in the radioresistant bacterium Deinococcus radiodurans. Biosystems 85: 99-106.
http://dx.doi.org/10.1016/j.biosystems.2005.12.003
PMid:16431014
Liu Q and Xue Q (2005). Comparative studies on codon usage pattern of chloroplasts and their host nuclear genes in four plant species. J. Genet. 84: 55-62.
http://dx.doi.org/10.1007/BF02715890
PMid:15876584
Liu Q, Feng Y, Zhao X, Dong H, et al. (2004). Synonymous codon usage bias in Oryza sativa. Plant Sci. 167: 101-105.
http://dx.doi.org/10.1016/j.plantsci.2004.03.003
Liu Q, Dou S, Ji Z and Xue Q (2005). Synonymous codon usage and gene function are strongly related in Oryza sativa. Biosystems 80: 123-131.
http://dx.doi.org/10.1016/j.biosystems.2004.10.008
PMid:15823411
Mitreva M, Wendl MC, Martin J, Wylie T, et al. (2006). Codon usage patterns in Nematoda: analysis based on over 25 million codons in thirty-two species. Genome Biol. 7: R75.
http://dx.doi.org/10.1186/gb-2006-7-8-r75
PMCid:1779591
Morton BR and Wright SI (2007). Selective constraints on codon usage of nuclear genes from Arabidopsis thaliana. Mol. Biol. Evol. 24: 122-129.
http://dx.doi.org/10.1093/molbev/msl139
PMid:17021276
Mukhopadhyay P, Basak S and Ghosh TC (2007a). Synonymous codon usage in different protein secondary structural classes of human genes: implication for increased non-randomness of GC3 rich genes towards protein stability. J. Biosci. 32: 947-963.
http://dx.doi.org/10.1007/s12038-007-0095-z
PMid:17914237
Mukhopadhyay P, Basak S and Ghosh TC (2007b). Nature of selective constraints on synonymous codon usage of rice differs in GC-poor and GC-rich genes. Gene 400: 71-81.
http://dx.doi.org/10.1016/j.gene.2007.05.027
PMid:17629420
Murray EE, Lotzer J and Eberle M (1989). Codon usage in plant genes. Nucleic Acids Res. 17: 477-498.
http://dx.doi.org/10.1093/nar/17.2.477
PMid:2644621 PMCid:331598
Naya H, Romero H, Carels N, Zavala A, et al. (2001). Translational selection shapes codon usage in the GC-rich genome of Chlamydomonas reinhardtii. FEBS Lett. 501: 127-130.
http://dx.doi.org/10.1016/S0014-5793(01)02644-8
Peraldi A, Beccari G, Steed A and Nicholson P (2011). Brachypodium distachyon: a new pathosystem to study Fusarium head blight and other Fusarium diseases of wheat. BMC Plant Biol. 11: 100.
http://dx.doi.org/10.1186/1471-2229-11-100
PMid:21639892 PMCid:3123626
Roychoudhury S and Mukherjee D (2010). A detailed comparative analysis on the overall codon usage pattern in herpesviruses. Virus Res. 148: 31-43.
http://dx.doi.org/10.1016/j.virusres.2009.11.018
PMid:19969032
Sharp PM and Li WH (1987). The codon Adaptation Index - a measure of directional synonymous codon usage bias, and its potential applications. Nucleic Acids Res. 15: 1281-1295.
http://dx.doi.org/10.1093/nar/15.3.1281
PMid:3547335 PMCid:340524
Sharp PM, Stenico M, Peden JF and Lloyd AT (1993). Codon usage: mutational bias, translational selection, or both? Biochem. Soc. Trans. 21: 835-841.
PMid:8132077
Shields DC and Sharp PM (1987). Synonymous codon usage in Bacillus subtilis reflects both translational selection and mutational biases. Nucleic Acids Res. 15: 8023-8040.
http://dx.doi.org/10.1093/nar/15.19.8023
PMid:3118331 PMCid:306324
Shields DC, Sharp PM, Higgins DG and Wright F (1988). "Silent" sites in Drosophila genes are not neutral: evidence of selection among synonymous codons. Mol. Biol. Evol. 5: 704-716.
PMid:3146682
Stenico M, Lloyd AT and Sharp PM (1994). Codon usage in Caenorhabditis elegans: delineation of translational selection and mutational biases. Nucleic Acids Res. 22: 2437-2446.
http://dx.doi.org/10.1093/nar/22.13.2437
PMid:8041603 PMCid:308193
Sueoka N (1988). Directional mutation pressure and neutral molecular evolution. Proc. Natl. Acad. Sci. U. S. A. 85: 2653-2657.
http://dx.doi.org/10.1073/pnas.85.8.2653
PMid:3357886 PMCid:280056
Sueoka N and Kawanishi Y (2000). DNA G+C content of the third codon position and codon usage biases of human genes. Gene 261: 53-62.
http://dx.doi.org/10.1016/S0378-1119(00)00480-7
Wang HC and Hickey DA (2007). Rapid divergence of codon usage patterns within the rice genome. BMC Evol. Biol. 7: S6.
http://dx.doi.org/10.1186/1471-2148-7-S1-S6
PMid:17288579 PMCid:1796615
Wright F (1990). The 'effective number of codons' used in a gene. Gene 87: 23-29.
http://dx.doi.org/10.1016/0378-1119(90)90491-9
Zhang WJ, Zhou J, Li ZF, Wang L, et al. (2007). Comparative analysis of codon usage patterns among mitochondrion, chloroplast and nuclear genes in Triticum aestivum L. J. Integr. Plant Biol. 49: 246-254.
http://dx.doi.org/10.1111/j.1744-7909.2007.00404.x
Zhao S, Zhang Q, Chen Z, Zhao Y, et al. (2007). The factors shaping synonymous codon usage in the genome of Burkholderia mallei. J. Genet. Genomics 34: 362-372.
http://dx.doi.org/10.1016/S1673-8527(07)60039-3