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

A U Rehman

Showing results (11-20 of 16) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 16 results.
Clinical Genetics|January 4, 2012
DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3R A Ali, A U Rehman, S N Khan, et al.
European Review for Medical and Pharmacological Sciences|April 30, 2021
In silico analysis of Naegleria fowleri cathepsin B paralogs: important drug targetsM Aurongzeb, S A Haq, Y Rashid, et al.
Lancet (London, England)|November 9, 1985
Brain water measured in volunteers after alcohol and vasopressinA J Mander, M A Smith, D M Kean, et al.
Tropical Biomedicine|October 5, 2021
Sero-epidemiology and risk factor analysis of human brucellosis in Punjab, Pakistan: a cross sectional studyZ Nawaz, M Shafique, M A Zahoor, et al.
Polish Journal of Veterinary Sciences|March 25, 2025
Seroprevalence and molecular characterization of lumpy skin disease virus in Bahawalpur district of South Punjab, PakistanA Nadeem, A Nasir, A U Rehman, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Clinical Genetics|January 4, 2012
DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3R A Ali, A U Rehman, S N Khan, et al.
European Review for Medical and Pharmacological Sciences|April 30, 2021
In silico analysis of Naegleria fowleri cathepsin B paralogs: important drug targetsM Aurongzeb, S A Haq, Y Rashid, et al.
Lancet (London, England)|November 9, 1985
Brain water measured in volunteers after alcohol and vasopressinA J Mander, M A Smith, D M Kean, et al.
Tropical Biomedicine|October 5, 2021
Sero-epidemiology and risk factor analysis of human brucellosis in Punjab, Pakistan: a cross sectional studyZ Nawaz, M Shafique, M A Zahoor, et al.
Polish Journal of Veterinary Sciences|March 25, 2025
Seroprevalence and molecular characterization of lumpy skin disease virus in Bahawalpur district of South Punjab, PakistanA Nadeem, A Nasir, A U Rehman, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Pageof 2