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话题： mutations更多

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Tumor-derived neomorphic mutations in ASXL1 impairs the BAP1-ASXL1-FOXK1/K2 transcription network
Yu-KunXia1,2,Yi-RongZeng1,2,Meng-LiZhang1,2,3,PengLiu1,2,FangLiu4,HaoZhang5,6,Chen-XiHe1,Yi-PingSun1,2,Jin-YeZhang1,2,ChengZhang1,2,LeiSong7,8,ChenDin ...
中科院生物物理研究所本站小编 Free考研考试 2022-01-02
Biallelic mutations in CDC20 cause female infertility characterized by abnormalit
LinZhao1,SongguoXue2,ZhongyuanYao3,JuanziShi4,BiaobangChen5,LingWu6,LihuaSun2,YaoXu2,ZhengYan6,BinLi6,XiaoyanMao6,JingFu7,ZhihuaZhang1,JianMu1,Wenjing ...
中科院生物物理研究所本站小编 Free考研考试 2022-01-02
Mutations in foregut SOX2+ cells induce efficient proliferation via CXCR2 pat
TomoakiHishida1,EricVazquez-Ferrer1,YurikoHishida-Nozaki1,IgnacioSancho-Martinez1,YutaTakahashi1,FumiyukiHatanaka1,JunWu1,AlejandroOcampo1,PradeepRedd ...
中科院生物物理研究所本站小编 Free考研考试 2022-01-02
Screening for mutations in human cardiomyopathy-is RBM24 a new but rare disease
AnnaGaertner,AndreasBrodehl,HendrikMiltingErichandHannaKlessmannInstitute,HeartandDiabetesCenterNRW,UniversityHospitaloftheRuhr-UniversityBochum,Georg ...
中科院生物物理研究所本站小编 Free考研考试 2022-01-02
Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear ma
XiulanSua,1,YufeiFengb,c,1,SofiaA.Rahmand,1,ShuilongWub,c,1,GuoanLib,c,FranzRüschendorfe,LeiZhaof,HongweiCuia,JunqingLiangg,LiangFange,h,HaoHui,Sebast ...
中科院遗传与发育生物学研究所本站小编 Free考研考试 2022-01-01
DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the W
LinglingLiua,b,WeiqiLiua,b,YanShia,LingLia,YunqianGaoa,YunpingLeic,RichardFinnella,c,TingZhangd,FengZhanga,b,LiJina,b,HuiliLif,WufanTaoa,g,HongyanWang ...
中科院遗传与发育生物学研究所本站小编 Free考研考试 2022-01-01
Mutations in TP53, ZNF750, and RB1 typify ocular sebaceous carcinoma
YongyangBao1,#,J.EvaSelfridge2,3,4,#,JanetWang5,6,#,YiqingZhao7,8,JunqiCui9,KishoreGuda10,ZhengheWang11,12,YanboZhu131DepartmentofPathology,TheNinthPe ...
中科院遗传与发育生物学研究所本站小编 Free考研考试 2022-01-01
Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia
WangjieLiua,b,c,#,HuanWud,e,f,#,LiWanga,#,XiaoyuYangg,ChunyuLiua,XiaojinHed,e,f,WeiyuLia,JiajiaWangd,e,f,YujieChend,e,f,HongyanWanga,YangGaod,e,f,Shuy ...
中科院遗传与发育生物学研究所本站小编 Free考研考试 2022-01-01
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话题： mutations更多

领限时大额优惠券,享本站正版考研考试资料!

Tumor-derived neomorphic mutations in ASXL1 impairs the BAP1-ASXL1-FOXK1/K2 transcription network

Biallelic mutations in <i>CDC20</i> cause female infertility characterized by abnormalit

Mutations in foregut SOX2<sup>+</sup> cells induce efficient proliferation via CXCR2 pat

Screening for mutations in human cardiomyopathy-is <em>RBM24</em> a new but rare disease

Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear ma

DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the W

Mutations in TP53, ZNF750, and RB1 typify ocular sebaceous carcinoma

Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia

VIP万种考研考证电子书、题库、视频随便看,每本不到一分钱!