Publications
Found 11 results
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“Molecular characterization and expression analysis of purple acid phosphatase gene from pearl oyster Pinctada martensii”, vol. 14, pp. 552-562, 2015.
, “Molecular cloning and expression analysis of a pearl oyster (Pinctada martensii) heat shock protein 90 (HSP90)”, vol. 14, pp. 18778-18791, 2015.
, “Single nucleotide polymorphism analysis of the endopolygalacturonase gene in peach and its potential use in crossbreeding programs”, vol. 14, pp. 4090-4101, 2015.
, “A single nucleotide polymorphism in the promoter region of let-7 family is associated with lung cancer risk in Chinese”, vol. 14, pp. 4505-4512, 2015.
, “Molecular characterization of tumor necrosis factor receptor-associated factor 6 (TRAF6) in pearl oyster Pinctada martensii”, vol. 13, pp. 10545-10555, 2014.
, “Critical evaluation of transcription factor Atf2 as a candidate modulator of alcohol preference in mouse and human populations”, vol. 12, pp. 5992-6005, 2013.
, “Potential role of Atp5g3 in epigenetic regulation of alcohol preference or obesity from a mouse genomic perspective”, vol. 12, pp. 3662-3674, 2013.
, “Molecular characterization, polymorphism of the ACOX1 gene and association with ultrasound traits in Bos taurus”, vol. 10, pp. 1948-1957, 2011.
, Brethour JR (1994). Estimating marbling score in live cattle from ultrasound images using pattern recognition and neural network procedures. J. Anim. Sci. 72: 1425-1432.
PMid:8071165
Casas-Carrillo E, Prill-Adams A, Price SG, Clutter AC, et al. (1997). Mapping genomic regions associated with growth rate in pigs. J. Anim. Sci. 75: 2047-2053.
PMid:9263050
Clop A, Ovilo C, Perez-Enciso M, Cercos A, et al. (2003). Detection of QTL affecting fatty acid composition in the pig. Mamm. Genome 14: 650-656.
http://dx.doi.org/10.1007/s00335-002-2210-7
PMid:14629115
Fan CY, Pan J, Chu R, Lee D, et al. (1996). Hepatocellular and hepatic peroxisomal alterations in mice with a disrupted peroxisomal fatty acyl-coenzyme A oxidase gene. J. Biol. Chem. 271: 24698-24710.
http://dx.doi.org/10.1074/jbc.271.40.24698
PMid:8798738
Fournier B, Saudubray JM, Benichou B, Lyonnet S, et al. (1994). Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy. J. Clin. Invest. 94: 526-531.
http://dx.doi.org/10.1172/JCI117365
PMid:8040306 PMCid:296126
Hamlin KE, Green RD, Cundiff LV, Wheeler TL, et al. (1995). Real-time ultrasonic measurement of fat thickness and longissimus muscle area: II. Relationship between real-time ultrasound measures and carcass retail yield. J. Anim. Sci. 73: 1725-1734.
PMid:7673066
Jiao Y, Zan LS, Liu YF, Wang HB, et al. (2010). A novel polymorphism of the MYPN gene and its association with meat quality traits in Bos taurus. Genet. Mol. Res. 9: 1751-1758.
http://dx.doi.org/10.4238/vol9-3gmr906
PMid:20812196
Kim S, Sohn I, Ahn JI, Lee KH, et al. (2004). Hepatic gene expression profiles in a long-term high-fat diet-induced obesity mouse model. Gene 340: 99-109.
http://dx.doi.org/10.1016/j.gene.2004.06.015
PMid:15556298
Lan XY, Pan CY, Chen H, Zhang CL, et al. (2007). An Alul PCR-RFLP detecting a silent allele at the goat POU1F1 locus and its association with production traits. Small Ruminant Res. 73: 8-12.
http://dx.doi.org/10.1016/j.smallrumres.2006.10.009
Li Y, Tharappel JC, Cooper S, Glenn M, et al. (2000). Expression of the hydrogen peroxide-generating enzyme fatty acyl CoA oxidase activates NF-kappaB. DNA Cell Biol. 19: 113-120.
http://dx.doi.org/10.1089/104454900314627
PMid:10701777
Liu YF, Zan LS, Li K, Zhao SP, et al. (2010). A novel polymorphism of GDF5 gene and its association with body measurement traits in Bos taurus and Bos indicus breeds. Mol. Biol. Rep. 37: 429-434.
http://dx.doi.org/10.1007/s11033-009-9604-5
PMid:19590978
Morais S, Knoll-Gellida A, Andre M, Barthe C, et al. (2007). Conserved expression of alternative splicing variants of peroxisomal acyl-CoA oxidase 1 in vertebrates and developmental and nutritional regulation in fish. Physiol. Genomics 28: 239-252.
http://dx.doi.org/10.1152/physiolgenomics.00136.2006
PMid:17090698
Mullenbach R, Lagoda PJ and Welter C (1989). An efficient salt-chloroform extraction of DNA from blood and tissues. Trends Genet. 5: 391.
PMid:2623762
Nohammer C, El-Shabrawi Y, Schauer S, Hiden M, et al. (2000). cDNA cloning and analysis of tissue-specific expression of mouse peroxisomal straight-chain acyl-CoA oxidase. Eur. J. Biochem. 267: 1254-1260.
http://dx.doi.org/10.1046/j.1432-1327.2000.01128.x
Oaxaca-Castillo D, Andreoletti P, Vluggens A, Yu S, et al. (2007). Biochemical characterization of two functional human liver acyl-CoA oxidase isoforms 1a and 1b encoded by a single gene. Biochem. Biophys. Res. Commun. 360: 314-319.
http://dx.doi.org/10.1016/j.bbrc.2007.06.059
PMid:17603022 PMCid:2732019
Rosewich H, Waterham HR, Wanders RJ, Ferdinandusse S, et al. (2006). Pitfall in metabolic screening in a patient with fatal peroxisomal beta-oxidation defect. Neuropediatrics 37: 95-98.
http://dx.doi.org/10.1055/s-2006-923943
PMid:16773508
Varanasi U, Chu R, Chu S, Espinosa R, et al. (1994). Isolation of the human peroxisomal acyl-CoA oxidase gene: organization, promoter analysis, and chromosomal localization. Proc. Natl. Acad. Sci. U. S. A. 91: 3107-3111.
http://dx.doi.org/10.1073/pnas.91.8.3107
Wanders RJ (2004). Peroxisomes, lipid metabolism, and peroxisomal disorders. Mol. Genet. Metab. 83: 16-27.
http://dx.doi.org/10.1016/j.ymgme.2004.08.016
PMid:15464416
Yue G, Schröffel JJ, Moser G, Bartenschlager H, et al. (2003). Linkage and QTL mapping for Sus scrofa chromosome 12. J. Anim. Breed. Genet. 120: 95-102.
http://dx.doi.org/10.1046/j.0931-2668.2003.00429.x
Zuo B, Yang H, Wang J, Lei MG, et al. (2007a). Molecular characterization, sequence variation and association with fat deposition traits of ACOX1 gene in pigs. J. Anim. Feed Sci. 16: 433-444.
Zuo B, Yang H, Lei MG, Li FE, et al. (2007b). Association of the polymorphism in GYS1 and ACOX1 genes with meat quality traits in pigs. Animal 1: 1243-1248.
http://dx.doi.org/10.1017/S1751731107000523
“Molecular cloning, characterization and association analysis of the promoter region of the bovine CDK6 gene”, vol. 10, pp. 1777-1786, 2011.
, Chang JG, Chiou SS, Perng LI, Chen TC, et al. (1992a). Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan. Blood 80: 1079-1082.
PMid:1323345
Chang JG, Chen PH, Chiou SS, Lee LS, et al. (1992b). Rapid diagnosis of P-thalassemia mutations in Chinese by naturally and amplified created restriction sites. Blood 80: 2092-2096.
PMid:1391961
Cram EJ, Liu BD, Bjeldanes LF and Firestone GL (2001). Indole-3-carbinol inhibits CDK6 expression in human MCF-7 breast cancer cells by disrupting Sp1 transcription factor interactions with a composite element in the CDK6 gene promoter. J. Biol. Chem. 276: 22332-22340.
http://dx.doi.org/10.1074/jbc.M010539200
PMid:11297539
Eiken HG, Odland E, Boman H, Skjelkvale L, et al. (1991). Application of natural and amplification created restriction sites for the diagnosis of PKU mutations. Nucleic Acids Res. 19: 1427-1430.
http://dx.doi.org/10.1093/nar/19.7.1427
PMid:1851292 PMCid:333896
Ericson KK, Krull D, Slomiany P and Grossel MJ (2003). Expression of cyclin-dependent kinase 6, but not cyclin-dependent kinase 4, alters morphology of cultured mouse astrocytes. Mol. Cancer Res. 1: 654-664.
PMid:12861051
Fujimoto T, Anderson K, Jacobsen SE, Nishikawa SI, et al. (2007). Cdk6 blocks myeloid differentiation by interfering with Runx1 DNA binding and Runx1-C/EBPalpha interaction. EMBO J. 26: 2361-2370.
http://dx.doi.org/10.1038/sj.emboj.7601675
PMid:17431401 PMCid:1864973
Gilbert RP, Bailey DR and Shannon NH (1993). Linear body measurements of cattle before and after 20 years of selection for postweaning gain when fed two different diets. J. Anim. Sci. 71: 1712-1720.
PMid:8349499
Grossel MJ and Hinds PW (2006). Beyond the cell cycle: a new role for Cdk6 in differentiation. J. Cell Biochem. 97: 485-493.
http://dx.doi.org/10.1002/jcb.20712
PMid:16294322
Gudbjartsson DF, Walters GB, Thorleifsson G, Stefansson H, et al. (2008). Many sequence variants affecting diversity of adult human height. Nat. Genet. 40: 609-615.
http://dx.doi.org/10.1038/ng.122
PMid:18391951
Hu MG, Deshpande A, Enos M, Mao D, et al. (2009). A requirement for cyclin-dependent kinase 6 in thymocyte development and tumorigenesis. Cancer Res. 69: 810-818.
http://dx.doi.org/10.1158/0008-5472.CAN-08-2473
PMid:19155308 PMCid:2636510
Johnson CD, Esquela-Kerscher A, Stefani G, Byrom M, et al. (2007). The let-7 microRNA represses cell proliferation pathways in human cells. Cancer Res. 67: 7713-7722.
http://dx.doi.org/10.1158/0008-5472.CAN-07-1083
PMid:17699775
Kohrt DM, Crary JI, Gocheva V, Hinds PW, et al. (2009). Distinct subcellular distribution of cyclin dependent kinase 6. Cell Cycle 8: 2837-2843.
http://dx.doi.org/10.4161/cc.8.17.9521
PMid:19667758 PMCid:2774137
Lettre G, Jackson AU, Gieger C, Schumacher FR, et al. (2008). Identification of ten loci associated with height highlights new biological pathways in human growth. Nat. Genet. 40: 584-591.
http://dx.doi.org/10.1038/ng.125
PMid:18391950 PMCid:2687076
Liu YF, Zan LS, Li K, Zhao SP, et al. (2010). A novel polymorphism of GDF5 gene and its association with body measurement traits in Bos taurus and Bos indicus breeds. Mol. Biol. Rep. 37: 429-434.
http://dx.doi.org/10.1007/s11033-009-9604-5
PMid:19590978
Lujambio A, Ropero S, Ballestar E, Fraga MF, et al. (2007). Genetic unmasking of an epigenetically silenced microRNA in human cancer cells. Cancer Res. 67: 1424-1429.
http://dx.doi.org/10.1158/0008-5472.CAN-06-4218
PMid:17308079
Mateescu RG, Zhang Z, Tsai K, Phavaphutanon J, et al. (2005). Analysis of allele fidelity, polymorphic information content, and density of microsatellites in a genome-wide screening for hip dysplasia in a crossbreed pedigree. J. Hered. 96: 847-853.
http://dx.doi.org/10.1093/jhered/esi109
PMid:16251522
Matushansky I, Radparvar F and Skoultchi AI (2003). CDK6 blocks differentiation: coupling cell proliferation to the block to differentiation in leukemic cells. Oncogene 22: 4143-4149.
http://dx.doi.org/10.1038/sj.onc.1206484
PMid:12833137
Mullenbach R, Lagoda PJ and Welter C (1989). An efficient salt-chloroform extraction of DNA from blood and tissues. Trends Genet. 5: 391.
PMid:2623762
Nafa K, Bessler M, Mason P, Vulliamy T, et al. (1996). Factor V Leiden mutation investigated by amplification created restriction enzyme site (ACRES) in PNH patients with and without thrombosis. Haematologica 81: 540-542.
PMid:9009443
Nei M and Roychoudhury AK (1974). Sampling variances of heterozygosity and genetic distance. Genetics 76: 379-390.
PMid:4822472 PMCid:1213072
Nei M and Li WH (1979). Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc. Natl. Acad. Sci. U. S. A. 76: 5269-5273.
http://dx.doi.org/10.1073/pnas.76.10.5269
Ogasawara T, Katagiri M, Yamamoto A, Hoshi K, et al. (2004a). Osteoclast differentiation by RANKL requires NF-kappaB-mediated downregulation of cyclin-dependent kinase 6 (Cdk6). J. Bone Miner. Res. 19: 1128-1136.
http://dx.doi.org/10.1359/jbmr.2004.19.7.1128
PMid:15176996
Ogasawara T, Kawaguchi H, Jinno S, Hoshi K, et al. (2004b). Bone morphogenetic protein 2-induced osteoblast differentiation requires Smad-mediated down-regulation of Cdk6. Mol. Cell Biol. 24: 6560-6568.
http://dx.doi.org/10.1128/MCB.24.15.6560-6568.2004
PMid:15254224 PMCid:444857
Peng Y, Chen F, Melamed J, Chiriboga L, et al. (2008). Distinct nuclear and cytoplasmic functions of androgen receptor cofactor p44 and association with androgen-independent prostate cancer. Proc. Natl. Acad. Sci. U. S. A. 105: 5236-5241.
http://dx.doi.org/10.1073/pnas.0712262105
PMid:18356297 PMCid:2278178
Rowell EA and Wells AD (2006). The role of cyclin-dependent kinases in T-cell development, proliferation, and function. Crit. Rev. Immunol. 26: 189-212.
PMid:16928186
Silber J, Lim DA, Petritsch C, Persson AI, et al. (2008). miR-124 and miR-137 inhibit proliferation of glioblastoma multiforme cells and induce differentiation of brain tumor stem cells. BMC Med. 6: 14.
http://dx.doi.org/10.1186/1741-7015-6-14
PMid:18577219 PMCid:2443372
Thomas JW, Lee-Lin SQ and Green ED (1999). Human-mouse comparative mapping of the genomic region containing CDK6: localization of an evolutionary breakpoint. Mamm. Genome 10: 764-767.
http://dx.doi.org/10.1007/s003359901088
PMid:10384057
Weedon MN, Lango H, Lindgren CM, Wallace C, et al. (2008). Genome-wide association analysis identifies 20 loci that influence adult height. Nat. Genet. 40: 575-583.
http://dx.doi.org/10.1038/ng.121
PMid:18391952 PMCid:2681221
Yang Z, Cao Y, Zhu X, Huang Y, et al. (2009). Znhit1 causes cell cycle arrest and down-regulates CDK6 expression. Biochem. Biophys. Res. Commun. 386: 146-152.
http://dx.doi.org/10.1016/j.bbrc.2009.05.139
PMid:19501046
Zhang X, Neganova I, Przyborski S, Yang C, et al. (2009). A role for NANOG in G1 to S transition in human embryonic stem cells through direct binding of CDK6 and CDC25A. J. Cell Biol. 184: 67-82.
http://dx.doi.org/10.1083/jcb.200801009
PMid:19139263 PMCid:2615089
“A novel polymorphism of the lactoferrin gene and its association with milk composition and body traits in dairy goats”, vol. 9, pp. 2199-2206, 2010.
, Brandl N, Zemann A, Kaupe I, Marlovits S, et al. (2010). Signal transduction and metabolism in chondrocytes is modulated by lactoferrin. Osteoarthritis Cartilage 18: 117-125.
http://dx.doi.org/10.1016/j.joca.2009.08.012
PMid:19747587
Bullen JJ (1972). Iron-binding proteins in milk and resistance to Escherichia coli infection in infants. Proc. R. Soc. Med. 65: 1086.
PMid:4568537 PMCid:1644425
Cohen MS, Britigan BE, French M and Bean K (1987). Preliminary observations on lactoferrin secretion in human vaginal mucus: variation during the menstrual cycle, evidence of hormonal regulation, and implications for infection with Neisseria gonorrhoeae. Am. J. Obstet. Gynecol. 157: 1122-1125.
PMid:3120589
Cornish J (2004). Lactoferrin promotes bone growth. Biometals 17: 331-335.
http://dx.doi.org/10.1023/B:BIOM.0000027713.18694.91
PMid:15222486
Cornish J, Grey AB, Naot D and Palmano KP (2005). Lactoferrin and bone: an overview of recent progress. Aust. J. Dairy Technol. 60: 53-57.
Gutteridge JM, Paterson SK, Segal AW and Halliwell B (1981). Inhibition of lipid peroxidation by the iron-binding protein lactoferrin. Biochem. J. 199: 259-261.
PMid:7337708 PMCid:1163360
Jenssen H and Hancock RE (2009). Antimicrobial properties of lactoferrin. Biochimie 91: 19-29.
http://dx.doi.org/10.1016/j.biochi.2008.05.015
PMid:18573312
Jeremy B (1995). Lactoferrin: a multifunctional immunoregulatory protein? Immunol. Today 16: 417-419.
http://dx.doi.org/10.1016/0167-5699(95)80016-6
Kim SJ, Sohn BH, Jeong S, Pak KW, et al. (1999). High-level expression of human lactoferrin in milk of transgenic mice using genomic lactoferrin sequence. J. Biochem. 126: 320-325.
http://dx.doi.org/10.1093/oxfordjournals.jbchem.a022452
PMid:10423524
Kinsella JE and Whitehead DM (1989). Proteins in whey: chemical, physical, and functional properties. Adv. Food Nutr. Res. 33: 343-438.
http://dx.doi.org/10.1016/S1043-4526(08)60130-8
Lan XY, Pan CY, Chen H and Zhang CL (2007). An AluI PCR-RFLP detecting a silent allele at the goat POU1F1 locus and its association with production traits. Small Ruminant Res. 73: 8-12.
http://dx.doi.org/10.1016/j.smallrumres.2006.10.009
Leon-Sicairos N, Canizalez-Roman A, de la Garza M, Reyes-Lopez M, et al. (2009). Bactericidal effect of lactoferrin and lactoferrin chimera against halophilic Vibrio parahaemolyticus. Biochimie 91: 133-140.
http://dx.doi.org/10.1016/j.biochi.2008.06.009
PMid:18625283
Li GH, Zhang Y, Sun DX and Li N (2004). Study on the polymorphism of bovine lactoferrin gene and its relationship with mastitis. Anim. Biotechnol. 15: 67-76.
http://dx.doi.org/10.1081/ABIO-120037899
PMid:15248601
Liu LH, Gladwell W and Teng CT (2002). Detection of exon polymorphisms in the human lactoferrin gene. Biochem. Cell Biol. 80: 17-22.
http://dx.doi.org/10.1139/o01-207
PMid:11908638
Livney YD (2010). Milk proteins as vehicles for bioactives. Curr. Opin. Colloid Interface Sci. 15: 73-83.
http://dx.doi.org/10.1016/j.cocis.2009.11.002
Masson PL, Heremans JF and Dive CH (1966). An iron-binding protein common to many external secretions. Clin. Chim. Acta 14: 735-739.
http://dx.doi.org/10.1016/0009-8981(66)90004-0
Mohamed JA, DuPont HL, Jiang ZD, Belkind-Gerson J, et al. (2007). A novel single-nucleotide polymorphism in the lactoferrin gene is associated with susceptibility to diarrhea in North American travelers to Mexico. Clin. Infect. Dis. 44: 945-952.
http://dx.doi.org/10.1086/512199
PMid:17342646
Nei M and Roychoudhury AK (1974). Sampling variances of heterozygosity and genetic distance. Genetics 76: 379-390.
PMid:4822472 PMCid:1213072
Nei M and Li WH (1979). Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc. Natl. Acad. Sci. U. S. A. 76: 5269-5273.
http://dx.doi.org/10.1073/pnas.76.10.5269
PMid:291943 PMCid:413122
Nichols BL, McKee KS, Henry JF and Putman M (1987). Human lactoferrin stimulates thymidine incorporation into DNA of rat crypt cells. Pediatr. Res. 21: 563-567.
http://dx.doi.org/10.1203/00006450-198706000-00011
PMid:3496579
Park I, Schaeffer E, Sidoli A, Baralle FE, et al. (1985). Organization of the human transferrin gene: direct evidence that it originated by gene duplication. Proc. Natl. Acad. Sci. U. S. A. 82: 3149-3153.
http://dx.doi.org/10.1073/pnas.82.10.3149
PMid:3858812 PMCid:397732
Teng CT, Pentecost BT, Marshall A, Solomon A, et al. (1987). Assignment of the lactotransferrin gene to human chromosome 3 and to mouse chromosome 9. Somat. Cell Mol. Genet. 13: 689-693.
http://dx.doi.org/10.1007/BF01534490
PMid:3478818
Teng CT, Pentecost BT, Chen YH, Newbold RR, et al. (1989). Lactotransferrin gene expression in the mouse uterus and mammary gland. Endocrinology 124: 992-999.
http://dx.doi.org/10.1210/endo-124-2-992
PMid:2463910
Williams J (1982). The evolution of transferrin. Trends Biochem. Sci. 7: 394-397.
http://dx.doi.org/10.1016/0968-0004(82)90183-9
Yamauchi K, Tomita M, Giehl TJ and Ellison RT III (1993). Antibacterial activity of lactoferrin and a pepsin-derived lactoferrin peptide fragment. Infect. Immun. 61: 719-728.
PMid:8423097 PMCid:302785
Yamauchi K, Wakabayashi H, Shin K and Takase M (2006). Bovine lactoferrin: benefits and mechanism of action against infections. Biochem. Cell Biol. 84: 291-296.
http://dx.doi.org/10.1139/o06-054
PMid:16936799
“A novel polymorphism of the MYPN gene and its association with meat quality traits in Bos taurus”, vol. 9, pp. 1751-1758, 2010.
, Bang ML, Mudry RE, McElhinny AS, Trombitas K, et al. (2001). Myopalladin, a novel 145-kilodalton sarcomeric protein with multiple roles in Z-disc and I-band protein assemblies. J. Cell Biol. 153: 413-427.
http://dx.doi.org/10.1083/jcb.153.2.413
PMid:11309420 PMCid:2169455
Brethour JR (1994). Estimating marbling score in live cattle from ultrasound images using pattern recognition and neural network procedures. J. Anim. Sci. 72: 1425-1432.
PMid:8071165
Davoli R, Braglia S, Lama B, Fontanesi L, et al. (2003). Mapping, identification of polymorphisms and analysis of allele frequencies in the porcine skeletal muscle myopalladin and titin genes. Cytogenet. Genome Res. 102: 152-156.
http://dx.doi.org/10.1159/000075741
PMid:14970695
Du DS, Zhai LW, Xu DA and Wang CD (2009). SNPs detection of EPOR & MYPN gene and association with meat quality traits in porcine. Acta Vet. Zootech. Sin. 36: 80-83.
Duboscq-Bidot L, Xu P, Charron P, Neyroud N, et al. (2008). Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy. Cardiovasc. Res. 77: 118-125.
http://dx.doi.org/10.1093/cvr/cvm015
PMid:18006477
Gilbert R, Cohen JA, Pardo S, Basu A, et al. (1999). Identification of the A-band localization domain of myosin binding proteins C and H (MyBP-C, MyBP-H) in skeletal muscle. J. Cell. Sci. 112 (Pt 1): 69-79.
PMid:9841905
Hamlin KE, Green RD, Cundiff LV, Wheeler TL, et al. (1995). Real-time ultrasonic measurement of fat thickness and longissimus muscle area: II. Relationship between real-time ultrasound measures and carcass retail yield. J. Anim. Sci. 73: 1725-1734.
PMid:7673066
Knoll R, Hoshijima M and Chien KR (2002). Z-line proteins: implications for additional functions. Eur. Heart J. Suppl. 4: I-13-I-17.
http://dx.doi.org/10.1016/S1520-765X(02)90105-7
Liu YF, Zan LS, Li K, Zhao SP, et al. (2010). A novel polymorphism of GDF5 gene and its association with body measurement traits in Bos taurus and Bos indicus breeds. Mol. Biol. Rep. 37: 429-434.
http://dx.doi.org/10.1007/s11033-009-9604-5
PMid:19590978
Ma K and Wang K (2002). Interaction of nebulin SH3 domain with titin PEVK and myopalladin: implications for the signaling and assembly role of titin and nebulin. FEBS Lett. 532: 273-278.
http://dx.doi.org/10.1016/S0014-5793(02)03655-4
McElhinny AS, Schwach C, Valichnac M, Mount-Patrick S, et al. (2003). Nebulin: the nebulous, multifunctional giant of striated muscle. Trends Cardiovasc. Med. 13: 195-201.
http://dx.doi.org/10.1016/S1050-1738(03)00076-8
Mestroni L (2009). Phenotypic heterogeneity of sarcomeric gene mutations: a matter of gain and loss? J. Am. Coll. Cardiol. 54: 343-345.
http://dx.doi.org/10.1016/j.jacc.2009.04.029
PMid:19608032 PMCid:2756576
Mullenbach R, Lagoda PJ and Welter C (1989). An efficient salt-chloroform extraction of DNA from blood and tissues. Trends Genet. 5: 391.
PMid:2623762
Nei M and Roychoudhury AK (1974). Sampling variances of heterozygosity and genetic distance. Genetics 76: 379-390.
PMid:4822472 PMCid:1213072
Nei M and Li WH (1979). Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc. Natl. Acad. Sci. U.S.A. 76: 5269-5273.
http://dx.doi.org/10.1073/pnas.76.10.5269
PMid:291943 PMCid:413122
Ohtsuka H, Yajima H, Maruyama K and Kimura S (1997). Binding of the N-terminal 63 kDa portion of connectin/titin to alpha-actinin as revealed by the yeast two-hybrid system. FEBS Lett. 401: 65-67.
http://dx.doi.org/10.1016/S0014-5793(96)01432-9
Otey CA, Rachlin A, Moza M, Arneman D, et al. (2005). The palladin/myotilin/myopalladin family of actin-associated scaffolds. Int. Rev. Cytol. 246: 31-58.
http://dx.doi.org/10.1016/S0074-7696(05)46002-7
Parast MM and Otey CA (2000). Characterization of palladin, a novel protein localized to stress fibers and cell adhesions. J. Cell. Biol. 150: 643-656.
http://dx.doi.org/10.1083/jcb.150.3.643
PMid:10931874 PMCid:2175193
Salmikangas P, Mykkanen OM, Gronholm M, Heiska L, et al. (1999). Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy. Hum. Mol. Genet. 8: 1329-1336.
http://dx.doi.org/10.1093/hmg/8.7.1329
PMid:10369880
Silvia MG, Daniel A and Carol AO (2008). The role of palladin in actin organization and cell motility. Cell Biol. 87: 517-525.
Sorimachi H, Freiburg A, Kolmerer B, Ishiura S, et al. (1997). Tissue-specific expression and alpha-actinin binding properties of the Z-disc titin: implications for the nature of vertebrate Z-discs. J. Mol. Biol. 270: 688-695.
http://dx.doi.org/10.1006/jmbi.1997.1145
PMid:9245597
Vaughan KT, Weber FE and Fischman DA (1992). cDNA cloning and sequence comparisons of human and chicken muscle C-protein and 86 kD protein. Symp. Soc. Exp. Biol. 46: 167-177.
PMid:1341033
Wang C, Huang ZH and Zhang XQ (2007). Analysis on associations of myopalladin gene polymorphisms with carcass traits in pigs. Acta Vet. Zootech. Sin. 38: 760-764.
Wimmers K, Murani E, Te Pas MF, Chang KC, et al. (2007). Associations of functional candidate genes derived from gene-expression profiles of prenatal porcine muscle tissue with meat quality and muscle deposition. Anim. Genet. 38: 474-484.
http://dx.doi.org/10.1111/j.1365-2052.2007.01639.x
PMid:17697135
Young P, Ferguson C, Banuelos S and Gautel M (1998). Molecular structure of the sarcomeric Z-disk: two types of titin interactions lead to an asymmetrical sorting of alpha-actinin. EMBO J. 17: 1614-1624.
http://dx.doi.org/10.1093/emboj/17.6.1614
PMid:9501083 PMCid:1170509