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Showing results (561-570 of 573) with videos related to

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Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi|November 24, 2021
[The enlightenment of foreign MD-MPH double degree program to the cultivation of high-level applied public health talents in China]X L Nie, L Zhuo, S F Wang, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 22, 2010
Gastroenteritis in a Taipei emergency department: aetiology and risk factorsC-C Lai, F-T Wu, D-D Ji, et al.
Bone Marrow Transplantation|October 18, 2011
Prospective study of one- vs two-unit umbilical cord blood transplantation following reduced intensity conditioning in adults with hematological malignanciesT L Kindwall-Keller, Y Hegerfeldt, H J Meyerson, et al.
Genome Biology|December 10, 2025
RAMEN: Dissecting individual, additive and interactive gene-environment contributions to DNA methylome variability in cord bloodErick I Navarro-Delgado, Darina Czamara, Karlie Edwards, et al.
Blood|July 5, 2022
Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancyMehul Sharma, Maggie P Fu, Henry Y Lu, et al.
Physical Review Letters|September 24, 2016
Nonlinear Transition from Mitigation to Suppression of the Edge Localized Mode with Resonant Magnetic Perturbations in the EAST TokamakY Sun, Y Liang, Y Q Liu, et al.
Journal of Clinical Immunology|April 28, 2025
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHADHenry Y Lu, Maryam Vaseghi-Shanjani, Avery J Lam, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|September 22, 2024
[Long-term hypomethylating agents in patients with myelodysplastic syndromes: a multi-center retrospective study]X Z Liu, S J Zhou, J Huang, et al.
The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.
The Journal of Experimental Medicine|March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic diseaseMehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Pageof 58

Showing results (561-570 of 573) with videos related to

Sort By:
Pageof 58
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi|November 24, 2021
[The enlightenment of foreign MD-MPH double degree program to the cultivation of high-level applied public health talents in China]X L Nie, L Zhuo, S F Wang, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|September 22, 2010
Gastroenteritis in a Taipei emergency department: aetiology and risk factorsC-C Lai, F-T Wu, D-D Ji, et al.
Bone Marrow Transplantation|October 18, 2011
Prospective study of one- vs two-unit umbilical cord blood transplantation following reduced intensity conditioning in adults with hematological malignanciesT L Kindwall-Keller, Y Hegerfeldt, H J Meyerson, et al.
Genome Biology|December 10, 2025
RAMEN: Dissecting individual, additive and interactive gene-environment contributions to DNA methylome variability in cord bloodErick I Navarro-Delgado, Darina Czamara, Karlie Edwards, et al.
Blood|July 5, 2022
Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancyMehul Sharma, Maggie P Fu, Henry Y Lu, et al.
Physical Review Letters|September 24, 2016
Nonlinear Transition from Mitigation to Suppression of the Edge Localized Mode with Resonant Magnetic Perturbations in the EAST TokamakY Sun, Y Liang, Y Q Liu, et al.
Journal of Clinical Immunology|April 28, 2025
A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHADHenry Y Lu, Maryam Vaseghi-Shanjani, Avery J Lam, et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|September 22, 2024
[Long-term hypomethylating agents in patients with myelodysplastic syndromes: a multi-center retrospective study]X Z Liu, S J Zhou, J Huang, et al.
The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.
The Journal of Experimental Medicine|March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic diseaseMehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Pageof 58