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Yufei Shi

Showing results (101-110 of 124) with videos related to

Pageof 13
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Environmental Science & Technology|April 1, 2026
Spatial Ice Confinement Enabled Chemical Reaction Acceleration for Water PurificationYufei Shi, Shaoze Xiao, Xuefei Zhou, et al.
Antimicrobial Agents and Chemotherapy|December 30, 2025
Population pharmacokinetics of caspofungin in critically ill Chinese children: a prospective observational studyNuo Xu, Yufei Shi, Gehang Ju, et al.
Pharmaceutics|June 27, 2024
Development and Quality Control of a Population Pharmacokinetic Model Library for CaspofunginNuo Xu, Yufei Shi, Yixue Wang, et al.
Bone|May 19, 2019
Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic ricketsHuda A BinEssa, Minjing Zou, Anwar F Al-Enezi, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Biallelic p.R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinomaHussein Raef, Roua Al-Rijjal, Sameerah Al-Shehri, et al.
International Journal of Endocrinology|August 13, 2015
A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible CardiomyopathyMohammad A Alqahtani, Ayed A Shati, Minjing Zou, et al.
Poultry Science|August 30, 2025
Genome-wide association study reveals candidate genes associated with egg-laying performance in Wuhua yellow chickenXunhe Huang, Zhipeng Zhong, Zhifeng Zhang, et al.
Orphanet Journal of Rare Diseases|February 26, 2021
Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostosesZayed Al-Zayed, Roua A Al-Rijjal, Lamya Al-Ghofaili, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|September 27, 2019
NOVEL <i>VDR</i> MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATIONKorcan Demir, Minjing Zou, Roua A Al-Rijjal, et al.
The Journal of Clinical Endocrinology and Metabolism|December 11, 2019
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic RicketsAyşe Nurcan Cebeci, Minjing Zou, Huda A BinEssa, et al.
Pageof 13

Showing results (101-110 of 124) with videos related to

Sort By:
Pageof 13
Environmental Science & Technology|April 1, 2026
Spatial Ice Confinement Enabled Chemical Reaction Acceleration for Water PurificationYufei Shi, Shaoze Xiao, Xuefei Zhou, et al.
Antimicrobial Agents and Chemotherapy|December 30, 2025
Population pharmacokinetics of caspofungin in critically ill Chinese children: a prospective observational studyNuo Xu, Yufei Shi, Gehang Ju, et al.
Pharmaceutics|June 27, 2024
Development and Quality Control of a Population Pharmacokinetic Model Library for CaspofunginNuo Xu, Yufei Shi, Yixue Wang, et al.
Bone|May 19, 2019
Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic ricketsHuda A BinEssa, Minjing Zou, Anwar F Al-Enezi, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Biallelic p.R2223H mutation in the thyroglobulin gene causes thyroglobulin retention and severe hypothyroidism with subsequent development of thyroid carcinomaHussein Raef, Roua Al-Rijjal, Sameerah Al-Shehri, et al.
International Journal of Endocrinology|August 13, 2015
A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible CardiomyopathyMohammad A Alqahtani, Ayed A Shati, Minjing Zou, et al.
Poultry Science|August 30, 2025
Genome-wide association study reveals candidate genes associated with egg-laying performance in Wuhua yellow chickenXunhe Huang, Zhipeng Zhong, Zhifeng Zhang, et al.
Orphanet Journal of Rare Diseases|February 26, 2021
Mutation spectrum of EXT1 and EXT2 in the Saudi patients with hereditary multiple exostosesZayed Al-Zayed, Roua A Al-Rijjal, Lamya Al-Ghofaili, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|September 27, 2019
NOVEL <i>VDR</i> MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATIONKorcan Demir, Minjing Zou, Roua A Al-Rijjal, et al.
The Journal of Clinical Endocrinology and Metabolism|December 11, 2019
Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic RicketsAyşe Nurcan Cebeci, Minjing Zou, Huda A BinEssa, et al.
Pageof 13