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

X Bu

Showing results (71-80 of 85) with videos related to

Pageof 9
Sort By:
The Journal of Clinical Investigation|March 1, 1997
Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypesG M Dallinga-Thie, M van Linde-Sibenius Trip, J I Rotter, et al.
The Journal of Laryngology and Otology|August 18, 2021
Ear fullness characteristics and prognosis in patients with all-frequency sudden sensorineural hearing lossE Zhou, X-P Xiao, B Liu, et al.
Journal of Neurochemistry|November 10, 2001
Oxidative impairment in scrapie-infected mice is associated with brain metals perturbations and altered antioxidant activitiesB S Wong, D R Brown, T Pan, et al.
Human Genetics|June 1, 1994
Linkage analysis of the genetic determinants of high density lipoprotein concentrations and composition: evidence for involvement of the apolipoprotein A-II and cholesteryl ester transfer protein lociX Bu, C H Warden, Y R Xia, et al.
Zhonghua Yi Xue Za Zhi|February 21, 2023
[Correlation between balloon volume and Meckel's cave size and its influence of percutaneous microballoon compression for trigeminal neuralgia]X C Fan, Z Y Lu, H Ren, et al.
American Journal of Medical Genetics|June 19, 1998
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutationY Bykhovskaya, M Shohat, K Ehrenman, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 18, 2001
Increased rate of apoptosis in intimal arterial smooth muscle cells through endogenous activation of TNF receptorsA Niemann-Jönsson, M P Ares, Z Q Yan, et al.
American Journal of Human Genetics|March 1, 1996
Multilocus genetic determinants of LDL particle size in coronary artery disease familiesJ I Rotter, X Bu, R M Cantor, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 6, 2022
[Disease spectrum analysis of children with inherited metabolic diseases detected by gas chromatography-mass spectrometry of urinary organic acids]X X Bu, W J Qiu, H W Zhang, et al.
Nature Genetics|July 1, 1993
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafnessT R Prezant, J V Agapian, M C Bohlman, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
The Journal of Clinical Investigation|March 1, 1997
Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypesG M Dallinga-Thie, M van Linde-Sibenius Trip, J I Rotter, et al.
The Journal of Laryngology and Otology|August 18, 2021
Ear fullness characteristics and prognosis in patients with all-frequency sudden sensorineural hearing lossE Zhou, X-P Xiao, B Liu, et al.
Journal of Neurochemistry|November 10, 2001
Oxidative impairment in scrapie-infected mice is associated with brain metals perturbations and altered antioxidant activitiesB S Wong, D R Brown, T Pan, et al.
Human Genetics|June 1, 1994
Linkage analysis of the genetic determinants of high density lipoprotein concentrations and composition: evidence for involvement of the apolipoprotein A-II and cholesteryl ester transfer protein lociX Bu, C H Warden, Y R Xia, et al.
Zhonghua Yi Xue Za Zhi|February 21, 2023
[Correlation between balloon volume and Meckel's cave size and its influence of percutaneous microballoon compression for trigeminal neuralgia]X C Fan, Z Y Lu, H Ren, et al.
American Journal of Medical Genetics|June 19, 1998
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutationY Bykhovskaya, M Shohat, K Ehrenman, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 18, 2001
Increased rate of apoptosis in intimal arterial smooth muscle cells through endogenous activation of TNF receptorsA Niemann-Jönsson, M P Ares, Z Q Yan, et al.
American Journal of Human Genetics|March 1, 1996
Multilocus genetic determinants of LDL particle size in coronary artery disease familiesJ I Rotter, X Bu, R M Cantor, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|June 6, 2022
[Disease spectrum analysis of children with inherited metabolic diseases detected by gas chromatography-mass spectrometry of urinary organic acids]X X Bu, W J Qiu, H W Zhang, et al.
Nature Genetics|July 1, 1993
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafnessT R Prezant, J V Agapian, M C Bohlman, et al.
Pageof 9