[1] |
WANG Xi, YE Ting, NIE Min, WU Xueyan, MAO Jiangfeng.
Beneficial effects of vemurafenib on craniopharyngioma carrying BRAF-V600E mutation
[J]. Basic & Clinical Medicine, 2024, 44(6): 866-872.
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[2] |
WANG Tingting, GUO Dan, LU Junyang, XU Lai, DONG Haitao, LIN Dianxin, XIAO Yi.
Analysis of cell mutation types of colorectal neuroendocrine tumors
[J]. Basic & Clinical Medicine, 2024, 44(4): 523-527.
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[3] |
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Diagnosis and treatment of tuberous sclerosis complex with TSC2 mosaic mutation and multiple angiomyolipomas:a case report
[J]. Basic & Clinical Medicine, 2024, 44(10): 1357-1362.
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[4] |
LIU Jingwen, SONG Haoxin, ZHU Lei.
Construction and drug resistance evaluation of cell strains which stably express FIP1L1-PDGFRA protein and its mutants
[J]. Basic & Clinical Medicine, 2024, 44(1): 63-68.
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[5] |
GONG Ziqi, WU Xiaowen, GUO Qian, GUO Jun, KONG Yan.
Influence of PTEN mutation on pathological features and prognosis of patients with mucosal melanoma
[J]. Basic & Clinical Medicine, 2023, 43(9): 1341-1345.
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[6] |
ZHANG Zhiyu, CAO Jun, LIANG Junbo.
Exploring the potential application of liver organoids of mouse as developmental models upon Hnf4α knockout
[J]. Basic & Clinical Medicine, 2023, 43(5): 724-732.
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[7] |
YANG Yufan, WANG Xi, NIE Min, WU Xueyan, MAO Jiangfeng.
Correlation between different FGFR1 mutations and congenital hypogonadotropic hypogonadism
[J]. Basic & Clinical Medicine, 2023, 43(5): 733-738.
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[8] |
LYU Xue, LI Xue-wei, YANG Ting, ZHENG Jin-xiu, ZHU Zi-he, YANG Tao, XU Jun.
Bioinformatic analysis of adenocarcinoma at esophagogastric junction and mutation sites screening of Involucrin gene
[J]. Basic & Clinical Medicine, 2022, 42(2): 235-242.
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[9] |
YANG Yu-fan, ZHAO Ya-ling, WANG Xi, NIE Min, WU Xue-yan, MAO Jiang-feng.
A case of micropenis caused by compound heterozygote mutations in luteinizing hormone/choriogonadotropin receptor (LHCGR)
[J]. Basic & Clinical Medicine, 2022, 42(10): 1492-1496.
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[10] |
TENG Cong-cong, XU Yong-mei, TANG Shu-ping, LI Yong, YANG Yang, LONG Lan, ZHANG Jie.
Epidemiological investigation of thalassemia in gestational age population of Dai nationality in Dehong Prefecture, Yunnan Province
[J]. Basic & Clinical Medicine, 2022, 42(10): 1504-1508.
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[11] |
CHEN Shi-kai, CHEN Jiu-ming, SUN Shun-chang.
Pathological mechanism of Charcot-Marie-Tooth disease caused by the Ile122Asn mutation in the C1orf194 gene
[J]. Basic & Clinical Medicine, 2021, 41(2): 159-164.
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[12] |
ZHANG Ning, MA Hui-hui, WANG Fan, LIANG Wei, WANG Yi-chun, WU Bing-shan, LI Qing-xin.
Correlations of MGMT promoter methylation and IDH1 mutations with the clinical prognosis of malignant glioma patients
[J]. Basic & Clinical Medicine, 2021, 41(10): 1476-1480.
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[13] |
ZHAO Ya-ling, LI Shu-ying, WANG Xi, NIE Min, WU Xue-yan, MAO Jiang-feng.
A case of Kabuki syndrome with precocious puberty and short stature due to novel KDM6A splice-site mutation
[J]. Basic & Clinical Medicine, 2021, 41(1): 8-12.
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[14] |
GAO Xiao-yan, LIU Shu-chuan.
Research advance on telomere shortening and bone marrow failure diseases
[J]. Basic & Clinical Medicine, 2021, 41(1): 116-119.
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[15] |
WANG Hui-ping, CHANG Xiao-yan, MA Xiao-sen, TONG An-li.
Whole-exome sequencing for a rare case of aldosterone-producing adrenocortical carcinoma
[J]. Basic & Clinical Medicine, 2020, 40(9): 1190-1194.
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