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Proceedings of the National Academy of Sciences of the United States of America
|
September 23, 2003
Probe selection for high-density oligonucleotide arrays
Rui Mei, Earl Hubbell, Stefan Bekiranov, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
December 16, 2021
Utilization and Comparative Effectiveness of Uterine Artery Embolization versus Hysterectomy for Severe Postpartum Hemorrhage: A National Inpatient Sample Study
Linzi A Webster, Janice Newsome, Mian Guo, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association
|
January 1, 1992
Family/media approach to HIV prevention: results with a home-based, parent-teen video program
R A Winett, E S Anderson, J F Moore, et al.
The American Journal of Managed Care
|
December 4, 2012
Utilization of HER2 genetic testing in a multi-institutional observational study
Katrina A B Goddard, Erin J Aiello Bowles, Heather Spencer Feigelson, et al.
Patient Preference and Adherence
|
April 21, 2020
Assessing Preferences for Rare Disease Treatment: Qualitative Development of the Paroxysmal Nocturnal Hemoglobinuria Patient Preference Questionnaire (PNH-PPQ<sup>©</sup>)
Karen Kaiser, Susan E Yount, Christa E Martens, et al.
Bioinformatics (Oxford, England)
|
December 12, 2003
Algorithms for large-scale genotyping microarrays
Wei-mn Liu, Xiaojun Di, Geoffrey Yang, et al.
Artificial Cells, Nanomedicine, and Biotechnology
|
November 17, 2017
Myocardial reparative functions of exosomes from mesenchymal stem cells are enhanced by hypoxia treatment of the cells via transferring microRNA-210 in an nSMase2-dependent way
Jinyun Zhu, Kai Lu, Ning Zhang, et al.
Gene Therapy
|
November 25, 2005
Activators of viral gene expression in polarized epithelial monolayers identified by rapid-throughput drug screening
E J Sorscher, J Harris, M Alexander, et al.
Clinical Genetics
|
February 6, 2010
Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation
M S Hildebrand, N P Thorne, C J Bromhead, et al.
The Laryngoscope
|
March 11, 2009
Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss
A Eliot Shearer, Michael S Hildebrand, Jennifer A Webster, et al.
Page
of 100
Search research articles
Search
Showing results (891-900 of 996) with videos related to
Sort By:
Page
of 100
Proceedings of the National Academy of Sciences of the United States of America
|
September 23, 2003
Probe selection for high-density oligonucleotide arrays
Rui Mei, Earl Hubbell, Stefan Bekiranov, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
December 16, 2021
Utilization and Comparative Effectiveness of Uterine Artery Embolization versus Hysterectomy for Severe Postpartum Hemorrhage: A National Inpatient Sample Study
Linzi A Webster, Janice Newsome, Mian Guo, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association
|
January 1, 1992
Family/media approach to HIV prevention: results with a home-based, parent-teen video program
R A Winett, E S Anderson, J F Moore, et al.
The American Journal of Managed Care
|
December 4, 2012
Utilization of HER2 genetic testing in a multi-institutional observational study
Katrina A B Goddard, Erin J Aiello Bowles, Heather Spencer Feigelson, et al.
Patient Preference and Adherence
|
April 21, 2020
Assessing Preferences for Rare Disease Treatment: Qualitative Development of the Paroxysmal Nocturnal Hemoglobinuria Patient Preference Questionnaire (PNH-PPQ<sup>©</sup>)
Karen Kaiser, Susan E Yount, Christa E Martens, et al.
Bioinformatics (Oxford, England)
|
December 12, 2003
Algorithms for large-scale genotyping microarrays
Wei-mn Liu, Xiaojun Di, Geoffrey Yang, et al.
Artificial Cells, Nanomedicine, and Biotechnology
|
November 17, 2017
Myocardial reparative functions of exosomes from mesenchymal stem cells are enhanced by hypoxia treatment of the cells via transferring microRNA-210 in an nSMase2-dependent way
Jinyun Zhu, Kai Lu, Ning Zhang, et al.
Gene Therapy
|
November 25, 2005
Activators of viral gene expression in polarized epithelial monolayers identified by rapid-throughput drug screening
E J Sorscher, J Harris, M Alexander, et al.
Clinical Genetics
|
February 6, 2010
Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation
M S Hildebrand, N P Thorne, C J Bromhead, et al.
The Laryngoscope
|
March 11, 2009
Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss
A Eliot Shearer, Michael S Hildebrand, Jennifer A Webster, et al.
Page
of 100