Publications
Found 5 results
Filters: Author is H.B. Zhang [Clear All Filters]
“Association of the VRK2 gene rs3732136 polymorphism with schizophrenia in a Northwest Chinese Han population”, vol. 14, pp. 9404-9411, 2015.
, “Regulators of G-protein signaling 9 genetic variations in Chinese subjects with schizophrenia”, vol. 14, pp. 8458-8465, 2015.
, “Polymorphisms in the endothelial nitric oxide synthase gene associated with recurrent miscarriage”, vol. 12, pp. 3879-3886, 2013.
, “Nine polymorphic STR loci in the HLA region in the Shaanxi Han population of China”, vol. 11, pp. 2534-2538, 2012.
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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.
http://dx.doi.org/10.1038/sj.ejhg.5201435
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.
http://dx.doi.org/10.1111/j.1399-0039.1997.tb02740.x
PMid:9098926
Foissac A, Salhi M and Cambon-Thomsen A (2000). Microsatellites in the HLA region: 1999 update. Tissue Antigens 55: 477-509.
http://dx.doi.org/10.1034/j.1399-0039.2000.550601.x
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.
http://dx.doi.org/10.1016/S0379-0738(97)00111-4
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.
http://dx.doi.org/10.1111/j.1399-0039.2004.00317.x
PMid:15496197
Guo SW and Thompson EA (1992). Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics 48: 361-372.
http://dx.doi.org/10.2307/2532296
PMid:1637966
Kashi Y and King DG (2006). Simple sequence repeats as advantageous mutators in evolution. Trends Genet. 22: 253-259.
http://dx.doi.org/10.1016/j.tig.2006.03.005
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.
http://dx.doi.org/10.1111/j.1744-313X.2007.00719.x
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.
http://dx.doi.org/10.1111/j.1399-0039.2006.759_6.x
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.
http://dx.doi.org/10.1046/j.1423-0410.1998.7410061.x
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.
http://dx.doi.org/10.1016/S1472-6483(10)62132-3
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.
http://dx.doi.org/10.1111/j.1744-313X.2009.00864.x
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.
http://dx.doi.org/10.1007/BF01247268
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.
“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.