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NET

2020-05-29

canlab (审核中...)

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#NET#

JAMA Netw Open：试管婴儿患癌风险比自然生产增加200%！出生缺陷比例也更高

2021-01-18

canlab (审核中...)

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JAMA Netw Open：肘管综合征选择哪一种减压手术更有效、更安全？

2021-06-24

canlab (审核中...)

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Infection, Genetics and Evolution：英国研究：新冠最早始于去年十月，“所有国家几乎同时传播”

2020-05-12

canlab (审核中...)

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#NET#

Blood：BTK抑制剂疗法可有效治疗venetoclax耐药性CLL

2020-08-24

canlab (审核中...)

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#NET#

JAMA Netw Open：坚持地中海饮食，2型糖尿病患病风险降低30%

2021-10-03

canlab (审核中...)

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#NET#

JAMA Network open：中国急性心肌梗死患者护理过程和结果的地理差异

2021-04-23

canlab (审核中...)

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#NET#

J Assist Reprod Genet：人工周期内冻融胚胎移植后妊娠并发症增加

2020-07-03

canlab (审核中...)

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J Med Genet：RIPOR2框内缺失是成年人听力损失发病的高频和高发原因

2021-01-18

canlab (审核中...)

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Epigenetics：组蛋白赖氨酸脱甲基酶KDM7A是胚胎正常发育所必需的

2020-10-15

canlab (审核中...)

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Nature Genetics：癌症的武器是“进化”？科学家发现癌基因在染色体外DNA中扩增，可促进肿瘤发展

2021-04-17

canlab (审核中...)

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#NET#

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Seattle Genetics公司的口服HER2抑制剂图卡替尼治疗乳腺癌，获得FDA的优先审查

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Cytokinetics的快速骨骼肌肌钙蛋白激活剂Reldesemtiv获得欧洲孤儿药称号，用于治疗肌萎缩性侧索硬化症

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PLoS Genet：THOC1缺失能够导致晚发非综合征听力损失

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JAMA Netw Open：参加磷酸二酯酶5抑制剂试验的男性勃起功能障碍患者的安慰剂反应

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Clin Epigenetics：口服维生素C可恢复血液恶性肿瘤患者的血浆维生素C的水平

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病例精讲：管中窥豹-JNET分型与工藤PP分型

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PLoS Genet：编码限制性羧基末端结构域的SLC12A2变异体能够引起人类遗传性听力损失

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NEJM：Venetoclax治疗急性髓性白血病（AML），III期临床取得正面结果

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Nature Genetics：颉伟/朱冰合作揭示DNA甲基化稳定且可塑性遗传的机制研究

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