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Nature Medicine
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January 19, 2024
Adjuvant sintilimab in resected high-risk hepatocellular carcinoma: a randomized, controlled, phase 2 trial
Kang Wang, Yan-Jun Xiang, Hong-Ming Yu, et al.
International Journal of Medical Sciences
|
March 9, 2026
Integrin αvβ3 is a Potential Therapeutic Target in Cholangiocarcinoma
Fitria Sari Wulandari, Chih-Yang Wang, Dana R Crawford, et al.
Journal of Human Genetics
|
December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosis
Mao Lin, Sen Zhao, Gang Liu, et al.
Cell Reports
|
September 25, 2012
TET1 suppresses cancer invasion by activating the tissue inhibitors of metalloproteinases
Chih-Hung Hsu, Kai-Lin Peng, Ming-Lun Kang, et al.
Surgical Endoscopy
|
February 5, 2026
The impact of microvascular invasion in tumor recurrence and survival after liver resection for non-B non-C hepatocellular carcinoma: a multicenter, propensity score-matched analysis
Chen Feng, Tian-Chen Zhang, Yu-Ting Wang, et al.
Human Genetics
|
July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
Jiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
Hepatobiliary Surgery and Nutrition
|
June 11, 2026
Prediction of postoperative early recurrence and response to adjuvant transcatheter arterial chemoembolization in hepatocellular carcinoma with microvascular invasion after hepatectomy: a multicenter study
Tian-Chen Zhang, Zhen-Qi Li, Wei-Li Jia, et al.
Nature Communications
|
May 2, 2024
Weyl spin-momentum locking in a chiral topological semimetal
Jonas A Krieger, Samuel Stolz, Iñigo Robredo, et al.
Human Mutation
|
September 1, 2019
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease
Weisheng Chen, Jiachen Lin, Lianlei Wang, et al.
Molecular Genetics & Genomic Medicine
|
November 28, 2019
Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1
Mao Lin, Zhenlei Liu, Gang Liu, et al.
Page
of 85
Search research articles
Search
Showing results (821-830 of 841) with videos related to
Sort By:
Page
of 85
Nature Medicine
|
January 19, 2024
Adjuvant sintilimab in resected high-risk hepatocellular carcinoma: a randomized, controlled, phase 2 trial
Kang Wang, Yan-Jun Xiang, Hong-Ming Yu, et al.
International Journal of Medical Sciences
|
March 9, 2026
Integrin αvβ3 is a Potential Therapeutic Target in Cholangiocarcinoma
Fitria Sari Wulandari, Chih-Yang Wang, Dana R Crawford, et al.
Journal of Human Genetics
|
December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosis
Mao Lin, Sen Zhao, Gang Liu, et al.
Cell Reports
|
September 25, 2012
TET1 suppresses cancer invasion by activating the tissue inhibitors of metalloproteinases
Chih-Hung Hsu, Kai-Lin Peng, Ming-Lun Kang, et al.
Surgical Endoscopy
|
February 5, 2026
The impact of microvascular invasion in tumor recurrence and survival after liver resection for non-B non-C hepatocellular carcinoma: a multicenter, propensity score-matched analysis
Chen Feng, Tian-Chen Zhang, Yu-Ting Wang, et al.
Human Genetics
|
July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
Jiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
Hepatobiliary Surgery and Nutrition
|
June 11, 2026
Prediction of postoperative early recurrence and response to adjuvant transcatheter arterial chemoembolization in hepatocellular carcinoma with microvascular invasion after hepatectomy: a multicenter study
Tian-Chen Zhang, Zhen-Qi Li, Wei-Li Jia, et al.
Nature Communications
|
May 2, 2024
Weyl spin-momentum locking in a chiral topological semimetal
Jonas A Krieger, Samuel Stolz, Iñigo Robredo, et al.
Human Mutation
|
September 1, 2019
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease
Weisheng Chen, Jiachen Lin, Lianlei Wang, et al.
Molecular Genetics & Genomic Medicine
|
November 28, 2019
Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1
Mao Lin, Zhenlei Liu, Gang Liu, et al.
Page
of 85