Found 5 results
Filters: Author is H.B. Zhang  [Clear All Filters]
H. B. Zhang, Wei, S. G., Yu, B., Li, L., and Lai, J. H., Nine polymorphic STR loci in the HLA region in the Shaanxi Han population of China, vol. 11, pp. 2534-2538, 2012.
Cullen M, Malasky M, Harding A and Carrington M (2003). High-density map of short tandem repeats across the human major histocompatibility complex. Immunogenetics 54: 900-910. PMid:12671742   Fiorentino F, Kahraman S, Karadayi H, Biricik A, et al. (2005). Short tandem repeats haplotyping of the HLA region in preimplantation HLA matching. Eur. J. Hum. Genet. 13: 953-958. PMid:15886713   Foissac A, Crouau-Roy B, Faure S, Thomsen M, et al. (1997). Microsatellites in the HLA region: on overview. Tissue Antigens 49: 197-214. PMid:9098926   Foissac A, Salhi M and Cambon-Thomsen A (2000). Microsatellites in the HLA region: 1999 update. Tissue Antigens 55: 477-509. PMid:10902606   Gill P, Brinkmann B, d'Aloja E, Andersen J, et al. (1997). Considerations from the European DNA profiling group (EDNAP) concerning STR nomenclature. Forensic Sci. Int. 87: 185-192.   Gourraud PA, Mano S, Barnetche T, Carrington M, et al. (2004). Integration of microsatellite characteristics in the MHC region: a literature and sequence based analysis. Tissue Antigens 64: 543-555. PMid:15496197   Guo SW and Thompson EA (1992). Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics 48: 361-372. PMid:1637966   Kashi Y and King DG (2006). Simple sequence repeats as advantageous mutators in evolution. Trends Genet. 22: 253-259. PMid:16567018   Korzebor A, Zamani M, Nouri K and Modarressi MH (2007). Statistical analysis of six STR loci located in MHC region in Iranian population for preimplantation genetic diagnosis. Int. J. Immunogenet. 34: 441-443. PMid:18001301   Malkki M, Gooley T, Horowitz M and Petersdorf EW (2007). MHC class I, II, and III microsatellite marker matching and survival in unrelated donor hematopoietic cell transplantation. Tissue Antigens 69 (Suppl 1): 46-49. PMid:17445162   Olaisen B, Bar W, Brinkmann B, Budowle B, et al. (1998). DNA recommendations 1997 of the international society for forensic genetics. Vox Sang. 74: 61-63. PMid:9481867   Rechitsky S, Kuliev A, Tur-Kaspa I, Morris R, et al. (2004). Preimplantation genetic diagnosis with HLA matching. Reprod. Biomed. Online 9: 210-221.   Schoske R, Vallone PM, Ruitberg CM and Butler JM (2003). Multiplex PCR design strategy used for the simultaneous amplification of 10 Y chromosome short tandem repeat (STR) loci. Anal. Bioanal. Chem. 375: 333-343. PMid:12589496   Sens-Abuazar C, Santos PS, Bicalho MG, Petzl-Erler ML, et al. (2009). MHC microsatellites in a Southern Brazilian population. Int. J. Immunogenet. 36: 269-274. PMid:19659935   Urquhart A, Kimpton CP, Downes TJ and Gill P (1994). Variation in short tandem repeat sequences--a survey of twelve microsatellite loci for use as forensic identification markers. Int. J. Legal Med. 107: 13-20. PMid:7999641   Walsh PS, Metzger DA and Higuchi R (1991). Chelex 100 as a medium for simple extraction of DNA for PCR-based typing from forensic material. Biotecchniqu06-513.
R. F. Sun, Zhu, Y. S., Feng, J. L., Tian, Z., Kuang, W. J., Liu, Y., Zhang, H. B., and Li, S. B., Polymorphisms of three new microsatellite sites of the dystrophin gene, vol. 10, pp. 744-751, 2011.
Ambrosio CE, Fadel L, Gaiad TP, Martins DS, et al. (2009). Identification of three distinguishable phenotypes in Golden Retriever muscular dystrophy. Genet. Mol. Res. 8: 389-396. doi:10.4238/vol8-2gmr581 Banks GB and Chamberlain JS (2008). The value of mammalian models for Duchenne muscular dystrophy in developing therapeutic strategies. Curr. Top. Dev. Biol. 84: 431-453. doi:10.1016/S0070-2153(08)00609-1 Basak J, Dasgupta UB, Banerjee TK, Senapati AK, et al. (2006). Analysis of dystrophin gene deletions by multiplex PCR in eastern India. Neurol. India 54: 310-311. doi:10.4103/0028-3886.27164 Davies KE (1997). Challenges in Duchenne muscular dystrophy. Neuromuscul. Disord. 7: 482-486. doi:10.1016/S0960-8966(97)00107-7 Den Dunnen JT, Grootscholten PM, Bakker E, Blonden LA, et al. (1989). Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. Am. J. Hum. Genet. 45: 835-847. Dubowitz V (2006). Enigmatic conflict of clinical and molecular diagnosis in Duchenne/Becker muscular dystrophy. Neuromuscul. Disord. 16: 865-866. doi:10.1016/j.nmd.2006.09.003 Gao Y and Li SB (2008). Effects of sample size on the observed number of allele of 9 STR loci with various genetic data. Yi Chuan 30: 313-320. doi:10.3724/SP.J.1005.2008.00313 Giliberto F, Ferreiro V, Dalamon V, Surace E, et al. (2003). Direct deletion analysis in two Duchenne muscular dystrophy symptomatic females using polymorphic dinucleotide (CA)n loci within the dystrophin gene. J. Biochem. Mol. Biol. 36: 179-184. doi:10.5483/BMBRep.2003.36.2.179 Kimmel M and Chakraborty R (1996). Measures of variation at DNA repeat loci under a general stepwise mutation model. Theor. Popul. Biol. 50: 345-367. doi:10.1006/tpbi.1996.0035 Koenig M, Hoffman EP, Bertelson CJ, Monaco AP, et al. (1987). Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50: 509-517. doi:10.1016/0092-8674(87)90504-6 Lai KK, Lo IF, Tong TM, Cheng LY, et al. (2006). Detecting exon deletions and duplications of the DMD gene using multiplex ligation-dependent probe amplification (MLPA). Clin. Biochem. 39: 367-372. doi:10.1016/j.clinbiochem.2005.11.019 Lai PS, Takeshima Y, Adachi K, Van Tran K, et al. (2002). Comparative study on deletions of the dystrophin gene in three Asian populations. J. Hum. Genet. 47: 552-555. doi:10.1007/s100380200084 Li Q and Wan JM (2005). SSRHunter: development of a local searching software for SSR sites. Yi Chuan 27: 808-810. Melis MA, Cau M, Muntoni F, Mateddu A, et al. (1998). Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families. Eur. J. Paediatr. Neurol. 2: 255-261. doi:10.1016/S1090-3798(98)80039-1 Mendell JR, Buzin CH, Feng J, Yan J, et al. (2001). Diagnosis of Duchenne dystrophy by enhanced detection of small mutations. Neurology 57: 645-650. Ribeiro Rodrigues EM, Leite FP, Hutz MH, Palha TJ, et al. (2008). A multiplex PCR for 11 X chromosome STR markers and population data from a Brazilian Amazon Region. Forensic Sci. Int. Genet. 2: 154-158. doi:10.1016/j.fsigen.2007.10.179 Roberts RG, Gardner RJ and Bobrow M (1994). Searching for the 1 in 2,400,000: a review of dystrophin gene point mutations. Hum. Mutat. 4: 1-11. doi:10.1002/humu.1380040102 Sewry CA (2010). Muscular dystrophies: an update on pathology and diagnosis. Acta Neuropathol. 120: 343-358. doi:10.1007/s00401-010-0727-5 Sifringer M, Uhlenberg B, Lammel S, Hanke R, et al. (2004). Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy. Hum. Genet. 114: 149-156. doi:10.1007/s00439-003-1041-2 Suminaga R, Takeshima Y, Adachi K, Yagi M, et al. (2002). A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5. J. Hum. Genet. 47: 196-201. doi:10.1007/s100380200023 Walmsley GL, Arechavala-Gomeza V, Fernandez-Fuente M, Burke MM, et al. (2010). A Duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient Cavalier King Charles Spaniels is amenable to exon 51 skipping. PLoS One 5: e8647. doi:10.1371/journal.pone.0008647 Yan J and Hou YP (2004). Exploring Novel STR Loci on Human Chromosome 21 for Forensic and Medical Genetics. Doctoral thesis, Sichuan University, Chengdu.