301) the manganese superoxide dismutase (SOD2) gene is a risk factor for primary angle cl |
302) In humans, this gene is located on chromosome 4 with 12 ex |
303) The results showed that the 12S rRNA gene is more variable than CO1. |
304) inding suggests that the embryonic STAT5A gene is primarily activated by maternal ge |
305) 0 and increased H3K27me3, contributing to gene silencing in bladder cancer cells. |
306) ges such as microRNAs (miRs)/Ago2-induced gene silencing represent complex molecular |
307) ional machinery and resulting in a robust gene silencing. |
308) cations involved in DNA methylation-based gene silencing. |
309) e contribution of functional SNPs in CD44 gene to AML susceptibility in eastern Chin |
310) lySia as well as variation in the ST8SIA2 gene to neuropsychiatric disorders, includ |
311) endothelial nitric oxide synthase (eNOS) gene to produce NO. |
312) y using partial mitochondrial 16 S rRNA gene, to estimate the order of inter- and |
313) ted by typical ATN codons, except for CO1 gene which is started by CAG codon. |
314) ed by typical ATN codons, except for cox1 gene which is started by CGA codon. |
315) pical ATN codon with the exception of COI gene which uses CGA as its initial codon; |
316) NOP2/Sun domain family, member 7 (Nsun7) gene, which encodes putative methyltransfe |
317) Gene alterations in known BBS (22) and oth |
318) ved an extremely high frequency of PIK3CA gene alterations (mutations, copy gains, o |
319) However, the significance of PIK3CA gene alterations with respect to clinicopa |
320) sequencing results obtained from the nad1 gene as a mitochondrial marker for the fir |
321) We confirmed that short fragment of cyt-b gene as a universal DNA barcode region. |
322) nd study to apply using of a cytochrome b gene as barcoding tool in distinguishing a |
323) The largest conserved gene block in N. |
324) ia: Balanidae), an inversion of one large gene block is identified (including three |
325) le mitogenomes reveals inversion of a six-gene block (trnP-nd4L-nd4-trnH-nd5-trnF) b |
326) C677T polymorphism (genotype TT) of MTHFR gene can be regarded as a genetic indicato |
327) nsversion mutation in exon 7 of the Nsun7 gene can be used as an infertility marker |
328) noviral transfection of the human insulin gene can be used for the construction of t |
329) bits for the first time, and compared its gene contents and genome organizations wit |
330) The gene contents of the mitogenome are identi |
331) The gene contents of the mitogenome are identi |
332) Apolipoprotein E (ApoE) gene polymorphisms are thought to be the m |
333) We evaluated the influence of the gene polymorphisms of CETP TaqIB (B1, B2) |
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