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The Journal of Clinical Endocrinology and Metabolism
|
October 17, 2014
Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome
Ender Karaca, Ramazan Buyukkaya, Davut Pehlivan, et al.
Journal of Medical Genetics
|
April 30, 2025
Rare missense variants in <i>FNDC1</i> are associated with severe adolescent idiopathic scoliosis
Wu-Lin Charng, Gabe Haller, Julia Whittle, et al.
Nanotechnology
|
December 29, 2020
Magnetotransport in hybrid InSe/monolayer graphene on SiC
Chih-Yuan Wang, Yun-Wu Lin, Chiashain Chuang, et al.
Genome Research
|
September 27, 2014
Large-scale identification of chemically induced mutations in Drosophila melanogaster
Nele A Haelterman, Lichun Jiang, Yumei Li, et al.
Journal of Cancer
|
March 12, 2019
The Upregulation of Trophinin-Associated Protein (TROAP) Predicts a Poor Prognosis in Hepatocellular Carcinoma
Hao Hu, Liang Xu, Yan Chen, et al.
ACS Applied Materials & Interfaces
|
May 19, 2021
Organic Lead Halide Nanocrystals Providing an Ultra-Wide Color Gamut with Almost-Unity Photoluminescence Quantum Yield
Shu-Wen Dai, Ying-Lin Lai, Lin Yang, et al.
Respiratory Research
|
July 31, 2020
Cell-specific expression of lung disease risk-related genes in the human small airway epithelium
Wu-Lin Zuo, Mahboubeh R Rostami, Shushila A Shenoy, et al.
ACS Nano
|
December 14, 2023
Harnessing 2D Ruddlesden-Popper Perovskite with Polar Organic Cation for Ultrasensitive Multibit Nonvolatile Transistor-Type Photomemristors
Po-Ting Lai, Cheng-Yueh Chen, Hao-Cheng Lin, et al.
Frontiers in Drug Delivery
|
September 29, 2023
Lyophilization Process Engineering and Thermostability of ID93 + GLA-SE, a Single-Vial Adjuvanted Subunit Tuberculosis Vaccine Candidate for Use in Clinical Studies
Timothy S Dutill, Michelle C Archer, Joseph McCollum, et al.
Nature Genetics
|
March 14, 2017
Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations
Xia Wang, Wu-Lin Charng, Chun-An Chen, et al.
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of 66
Search research articles
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Showing results (631-640 of 660) with videos related to
Sort By:
Page
of 66
The Journal of Clinical Endocrinology and Metabolism
|
October 17, 2014
Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome
Ender Karaca, Ramazan Buyukkaya, Davut Pehlivan, et al.
Journal of Medical Genetics
|
April 30, 2025
Rare missense variants in <i>FNDC1</i> are associated with severe adolescent idiopathic scoliosis
Wu-Lin Charng, Gabe Haller, Julia Whittle, et al.
Nanotechnology
|
December 29, 2020
Magnetotransport in hybrid InSe/monolayer graphene on SiC
Chih-Yuan Wang, Yun-Wu Lin, Chiashain Chuang, et al.
Genome Research
|
September 27, 2014
Large-scale identification of chemically induced mutations in Drosophila melanogaster
Nele A Haelterman, Lichun Jiang, Yumei Li, et al.
Journal of Cancer
|
March 12, 2019
The Upregulation of Trophinin-Associated Protein (TROAP) Predicts a Poor Prognosis in Hepatocellular Carcinoma
Hao Hu, Liang Xu, Yan Chen, et al.
ACS Applied Materials & Interfaces
|
May 19, 2021
Organic Lead Halide Nanocrystals Providing an Ultra-Wide Color Gamut with Almost-Unity Photoluminescence Quantum Yield
Shu-Wen Dai, Ying-Lin Lai, Lin Yang, et al.
Respiratory Research
|
July 31, 2020
Cell-specific expression of lung disease risk-related genes in the human small airway epithelium
Wu-Lin Zuo, Mahboubeh R Rostami, Shushila A Shenoy, et al.
ACS Nano
|
December 14, 2023
Harnessing 2D Ruddlesden-Popper Perovskite with Polar Organic Cation for Ultrasensitive Multibit Nonvolatile Transistor-Type Photomemristors
Po-Ting Lai, Cheng-Yueh Chen, Hao-Cheng Lin, et al.
Frontiers in Drug Delivery
|
September 29, 2023
Lyophilization Process Engineering and Thermostability of ID93 + GLA-SE, a Single-Vial Adjuvanted Subunit Tuberculosis Vaccine Candidate for Use in Clinical Studies
Timothy S Dutill, Michelle C Archer, Joseph McCollum, et al.
Nature Genetics
|
March 14, 2017
Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations
Xia Wang, Wu-Lin Charng, Chun-An Chen, et al.
Page
of 66