Results 141 to 150 of about 157,921 (154)

Bioinformatics analysis of a <i>CLCN5</i> geneframeshift mutation in a patient with Dent disease. [PDF]

Zhong Nan Da Xue Xue Bao Yi Xue Ban
Zhang Y, Li N, Fan L, Liu J.
europepmc   +1 more source

[Application Value of Neoadjuvant Targeted Therapy in Patients with EGFR-mutant 
Resectable Lung Adenocarcinoma]. [PDF]

Zhongguo Fei Ai Za Zhi
Huang S, Fan M, Peng K, Yan W, Chen B, Wang W, Yang T, Chen K, Kang M, Xie J.   +9 more
europepmc   +1 more source

[Clinical application value of detecting the mutation load of the FLT3-ITD gene before allogeneic hematopoietic stem cell transplantation using PCR-NGS technology]. [PDF]

Zhonghua Xue Ye Xue Za Zhi
Shao YC, Zhang YX, Sun WL, Lu H, Jiang CH, Wang LX, Huang JY, Zhang ZL, Lu HY, Pan ZK, Zhu WW, Hu XX.   +11 more
europepmc   +1 more source

[A Case of Metastatic Non-small Cell Lung Cancer with Rare BRAF p.L485_T488delinsF Mutation Treated with Dabrafenib and Trametinib]. [PDF]

Zhongguo Fei Ai Za Zhi
Wang Y, Zhao W, Yang C, Zhang R, Wang C, Han C, Li J.   +6 more
europepmc   +1 more source

[A Novel <i>rpsE</i> Mutation Mediates High-Level Spectinomycin Resistance in <i>Neisseria gonorrhoeae</i> and Influences Their Biological Fitness]. [PDF]

Sichuan Da Xue Xue Bao Yi Xue Ban
Li M, Yang G, Wang Y, Yong G, Wang H.
europepmc   +1 more source

A novel PAX9 variant in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9variants. [PDF]

Hua Xi Kou Qiang Yi Xue Za Zhi
Jin Z, Guo J, Yuan Y, Meng L, Li H, Zhao Y, Ren J, Ma Y, Xiao ZS, Zhang H, Yang L, Dou C, Wang X, Wang J, Shen W.   +14 more
europepmc   +1 more source

[The role of AKT inhibitors combined with Ruxolitinib in ameliorating myeloproliferative disorders in mice with CALR gene mutations]. [PDF]

Zhonghua Xue Ye Xue Za Zhi
Zhang LW, Zhang QG, Ji MC, Qi KM, Li ZY, Xu KL, Fu CL.   +6 more
europepmc   +1 more source

[Construction of a prognosis forecasting model for immuno-therapy response in cancer patients by integrating routine clinical parameters and tumor mutational burden]. [PDF]

Zhejiang Da Xue Xue Bao Yi Xue Ban
Zhu X, Hao S, Cheng Z, Fang W.
europepmc   +1 more source

[A case report of mild hereditary hemochromatosis caused by HAMP gene mutation]. [PDF]

Zhonghua Gan Zang Bing Za Zhi
Wang Z, Hou W, Zheng H.
europepmc   +1 more source

[A family report on congenital fibrosis of extraocular muscles syndrome caused by <i>TUBB3</i> gene mutation]. [PDF]

Zhong Nan Da Xue Xue Bao Yi Xue Ban
Li M, Qi X, Li Y, Tong B.
europepmc   +1 more source