Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Fang Fu

Showing results (291-300 of 315) with videos related to

Pageof 32
Sort By:
Genes|December 23, 2022
The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective StudyFang Fu, Ru Li, Qiu-Xia Yu, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 22, 2008
In vivo interstitial migration of primitive macrophages mediated by JNK-matrix metalloproteinase 13 signaling in response to acute injuryYong Zhang, Xue-Tao Bai, Kang-Yong Zhu, et al.
American Journal of Translational Research|February 10, 2018
NDUFA4 enhances neuron growth by triggering growth factors and inhibiting neuron apoptosis through Bcl-2 and cytochrome C mediated signaling pathwayFang Fu, Yan Li, Ru Li, et al.
Human Genetics|April 24, 2023
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencingRuibin Huang, Fang Fu, Hang Zhou, et al.
Heliyon|September 17, 2024
Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature reviewRuibin Huang, Chunling Ma, Huanyi Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 6, 2021
[Application of whole exome sequencing technology in fetuses with congenital structural abnormalities]Lushan Li, Fang Fu, Ru Li, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 14, 2022
Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testingJunhui Wan, Ru Li, Fatao Li, et al.
American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlationsRuibin Huang, Fang Fu, Fei Guo, et al.
Heliyon|March 16, 2023
Artificial intelligence-based computer-aided diagnosis system supports diagnosis of lymph node metastasis in esophageal squamous cell carcinoma: A multicenter studyShuai-Tong Zhang, Si-Yun Wang, Jie Zhang, et al.
Viral Immunology|June 6, 2015
Improvement of the Immunogenicity of Porcine Circovirus Type 2 DNA Vaccine by Recombinant ORF2 Gene and CpG MotifsJun Li, Jian-Li Shi, Xiao-Yan Wu, et al.
Pageof 32

Showing results (291-300 of 315) with videos related to

Sort By:
Pageof 32
Genes|December 23, 2022
The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective StudyFang Fu, Ru Li, Qiu-Xia Yu, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 22, 2008
In vivo interstitial migration of primitive macrophages mediated by JNK-matrix metalloproteinase 13 signaling in response to acute injuryYong Zhang, Xue-Tao Bai, Kang-Yong Zhu, et al.
American Journal of Translational Research|February 10, 2018
NDUFA4 enhances neuron growth by triggering growth factors and inhibiting neuron apoptosis through Bcl-2 and cytochrome C mediated signaling pathwayFang Fu, Yan Li, Ru Li, et al.
Human Genetics|April 24, 2023
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencingRuibin Huang, Fang Fu, Hang Zhou, et al.
Heliyon|September 17, 2024
Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature reviewRuibin Huang, Chunling Ma, Huanyi Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 6, 2021
[Application of whole exome sequencing technology in fetuses with congenital structural abnormalities]Lushan Li, Fang Fu, Ru Li, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 14, 2022
Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testingJunhui Wan, Ru Li, Fatao Li, et al.
American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlationsRuibin Huang, Fang Fu, Fei Guo, et al.
Heliyon|March 16, 2023
Artificial intelligence-based computer-aided diagnosis system supports diagnosis of lymph node metastasis in esophageal squamous cell carcinoma: A multicenter studyShuai-Tong Zhang, Si-Yun Wang, Jie Zhang, et al.
Viral Immunology|June 6, 2015
Improvement of the Immunogenicity of Porcine Circovirus Type 2 DNA Vaccine by Recombinant ORF2 Gene and CpG MotifsJun Li, Jian-Li Shi, Xiao-Yan Wu, et al.
Pageof 32