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Blood
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January 26, 2022
Severely impaired CTL killing is a feature of the neurological disorder Niemann-Pick disease type C1
Daniela Castiblanco, Jesse A Rudd-Schmidt, Tahereh Noori, et al.
Blood
|
May 22, 2013
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project
Jill M Johnsen, Paul L Auer, Alanna C Morrison, et al.
Environment International
|
January 8, 2026
Evaluating the effects of heat strain and air pollution on kidney health
Jaime Butler-Dawson, Diana Jaramillo, Lyndsay Krisher, et al.
Nature Communications
|
April 7, 2026
Modelling synaptic dysfunction in childhood dementia using human iPSC-derived cortical networks
Paris Mazzachi, Ella McDonald, Zarina Greenberg, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 3, 2011
Discovery of a highly potent series of TLR7 agonists
Peter Jones, David C Pryde, Thien-Duc Tran, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
May 13, 2026
Strategic consensus on the clinical translation of advanced therapies in paediatric rare neurological disorders
Natalie Y Lim, Christian E Meagher, Ann Bye, et al.
BMJ Open
|
March 11, 2026
NewbornsInSA multi-omic newborn screening: protocol for a prospective cohort study
Lucy Anastasi, Ayesha Chowdhury, Alex Ashenden, et al.
Internal Medicine Journal
|
March 13, 2026
An Australian standard of care for Niemann-Pick disease type C
Michel Tchan, Nicholas Smith, Heidi Peters, et al.
NPJ Genomic Medicine
|
February 10, 2026
Semi-automated genomic newborn screening highlights complexities in reporting
Ayesha Chowdhury, Shashikanth Marri, Lucy Anastasi, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 23, 2011
Design and optimisation of orally active TLR7 agonists for the treatment of hepatitis C virus infection
Thien-Duc Tran, David C Pryde, Peter Jones, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 149) with videos related to
Sort By:
Page
of 15
Blood
|
January 26, 2022
Severely impaired CTL killing is a feature of the neurological disorder Niemann-Pick disease type C1
Daniela Castiblanco, Jesse A Rudd-Schmidt, Tahereh Noori, et al.
Blood
|
May 22, 2013
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project
Jill M Johnsen, Paul L Auer, Alanna C Morrison, et al.
Environment International
|
January 8, 2026
Evaluating the effects of heat strain and air pollution on kidney health
Jaime Butler-Dawson, Diana Jaramillo, Lyndsay Krisher, et al.
Nature Communications
|
April 7, 2026
Modelling synaptic dysfunction in childhood dementia using human iPSC-derived cortical networks
Paris Mazzachi, Ella McDonald, Zarina Greenberg, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 3, 2011
Discovery of a highly potent series of TLR7 agonists
Peter Jones, David C Pryde, Thien-Duc Tran, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
May 13, 2026
Strategic consensus on the clinical translation of advanced therapies in paediatric rare neurological disorders
Natalie Y Lim, Christian E Meagher, Ann Bye, et al.
BMJ Open
|
March 11, 2026
NewbornsInSA multi-omic newborn screening: protocol for a prospective cohort study
Lucy Anastasi, Ayesha Chowdhury, Alex Ashenden, et al.
Internal Medicine Journal
|
March 13, 2026
An Australian standard of care for Niemann-Pick disease type C
Michel Tchan, Nicholas Smith, Heidi Peters, et al.
NPJ Genomic Medicine
|
February 10, 2026
Semi-automated genomic newborn screening highlights complexities in reporting
Ayesha Chowdhury, Shashikanth Marri, Lucy Anastasi, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 23, 2011
Design and optimisation of orally active TLR7 agonists for the treatment of hepatitis C virus infection
Thien-Duc Tran, David C Pryde, Peter Jones, et al.
Page
of 15