Results 41 to 50 of about 976,356 (101)
Rare Metals, Volume 45, Issue 6, June 2026.ABSTRACT The strength and ductility trade‐off in titanium matrix composites (TMCs) is a critical factor limiting their widespread application. In this study, a (TiB + TiC)/Ti–6Al–4V composite with an optimal balance between strength and ductility was engineered via multi‐directional forging.
Chunyu Shen +8 more
wiley +1 more source
Zhongguo shiyan zhenduanxue, 1997 采用银染ＰＣＲ－ＳＳＣＰ法检测肠癌细胞株及３０例新鲜肠癌Ｐ５３基因突变。结果发现ＬＯＶＯ细胞ｐ５３基因外显子５、６、７发生突变，ＬＳ１７４Ｔ细胞Ｐ５３基因的外显子５、８发生突变，３０例新鲜肿瘤标本ｐ５３基因外显子５、６、７、８的突变例数各为４、０、４、４例。大肠癌Ｐ５３基因突变热点为外显子５、７、８。
欧启水 +4 more
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Veterinary Dermatology, Volume 37, Issue 3, Page 353-364, June 2026.ABSTRACT Background Canine atopic dermatitis (cAD) is a multifactorial, inherited skin disease, estimated to affect ≤ 15% of dogs. Studies of skin messenger mRNA in cAD currently use invasive methods, including blood sampling and biopsy collection, whilst advances in human atopic dermatitis study methodology have demonstrated reliable use of minimally ...
Xavier Langon +5 more
wiley +1 more source
ABCA12 Frameshift Deletion in Domestic Cats With Ichthyosis Fetalis
Veterinary Dermatology, Volume 37, Issue 3, Page 365-374, June 2026.ABSTRACT Background Ichthyosis fetalis (IF), also known as harlequin ichthyosis, is a rare and often fatal autosomal recessive congenital skin disorder. It is characterized by thickened, hard skin plaques and deep skin fissures that limit mobility and cause malformations of the eyes, lips and ears.
Jeanna M. Blake +2 more
wiley +1 more source
, 2019 目的探讨1例马凡综合征患者原纤维蛋白1（FBN1）基因突变情况。方法收集1例临床确诊马凡综合征患者的临床资料,提取基因组DNA,进行目标区域捕获测序确定突变基因的位点;对候选的突变位点采用Sanger测序进行验证,同时在家系中进一步验证;分析FBN1基因突变对蛋白结构的影响。结果目标区域捕获测序结果显示先证者携带FBN1基因c.20232026delTTTG突变,该突变导致FBN1基因生成缩短并变异的RNA以及蛋白。家系验证显示患者父母不具有该突变,判断该突变为新生突变（denovo突变 ...
倪二茹 +5 more
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Rare Metals, Volume 45, Issue 4, April 2026.ABSTRACT Soft‐magnetic materials (SMMs) are indispensable for electrification and sustainable energy systems, yet their inherent mechanical fragility fundamentally limits applications under severe mechanical stresses. Enhancing the yield strength of SMMs is essential to prevent the degradation in magnetic performance and failure from plastic ...
Nairan Wang +6 more
wiley +1 more source
, 1997 摘 要 用聚合酶链反应- 单链构象多态性( PC R-SSCP) 、DN A直接测序和多重PCR法,检测了18例慢 性粒细胞白血病( CML) , 1 例K562细胞株, 9例急性粒细胞性白血病( AM L) , 6 例急性淋巴细胞性白血病 ( ALL) , 2例多发性骨髓瘤( MM)患者外周血/培养细胞DN A中P16基因的点突变和基因缺失。用PCR-SSC P 共筛查出5例CML中P16基因的异常,突变率为27.
李 巍 杜传书
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Zhongguo shiyan zhenduanxue, 2017 目的分析吉林省耐多药结核分枝杆菌临床分离株rpoB、katG基因突变特点,为建立本省快速耐多药检测方法提供参考。方法对吉林省耐多药结核分枝杆菌菌株扩增rpoB、katG基因测序后比对分析。结果耐多药结核分枝杆菌rpoB、katG基因的突变率分别为83.53%和70.6%,突变类型包括点突变、联合突变和缺失。在rpoB基因中,82.30%突变发生在RRDR区域,最常见突变位点为rpoB 531、rpoB 526、rpoB 516。KatG基因突变率为70.6%,最常见突变位点为katG315 ...
张炜煜 +4 more
doaj
Conservation Biology, Volume 40, Issue 2, April 2026.Abstract Wildlife reintroductions are socioecological processes entailing the intentional movement of organisms by people. In animal reintroductions, there is growing recognition of the importance of human dimensions and efforts to integrate these into reintroduction projects. To conceptually reframe reintroductions as processes of renewed coexistence (
Roger Edward Auster +3 more
wiley +1 more source
转突变型A53Tα-突触核蛋白基因的帕金森模型小鼠中脑的全基因组甲基化测序分析 [PDF]
, 2020 【目的】研究帕金森氏病（PD）致病基因SNCA在A53T位置突变后对转基因小鼠中脑多巴胺，神经元DNA甲基化修饰的影响。【方法】分别取转突变的人源α-突触核蛋白（hα-syn）即hA53Tα-syn基因小鼠和对照组小鼠的中脑组织，采用重亚硫酸盐测序法（BS-seq）分别对12月龄的转基因小鼠和非转基因（nTg）小鼠进行全基因组甲基化分析，随后筛选出差异甲基化区域（DMR）用于GO富集分析。【结果】通过对比分析，我们总计发现481个DMR，其中高甲基化与低甲基化DMR分别有257和224个 ...
林贤, 刘琳, 吴婷, 黎昭
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