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American Journal of Human Genetics
|
August 27, 2024
Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression
Samantha Malka, Pooja Biswas, Anne-Marie Berry, et al.
Journal of Neurointerventional Surgery
|
August 27, 2020
International experience of mechanical thrombectomy during the COVID-19 pandemic: insights from STAR and ENRG
Sami Al Kasab, Eyad Almallouhi, Ali Alawieh, et al.
Nature Machine Intelligence
|
June 26, 2025
Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene
Nikolas Pontikos, William A Woof, Siying Lin, et al.
Journal of Medicinal Chemistry
|
September 17, 2025
Fragment-Based Discovery and Structure-Led Optimization of MSC778, the First Potent, Selective, and Orally Bioavailable FEN1 Inhibitor
Sam E Mann, Julien Lefranc, Omar Alkhatib, et al.
Nature
|
April 5, 2016
sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance
Amanpreet Kaur, Marie R Webster, Katie Marchbank, et al.
The New England Journal of Medicine
|
November 20, 2024
Adjunctive Middle Meningeal Artery Embolization for Subdural Hematoma
Jason M Davies, Jared Knopman, Maxim Mokin, et al.
AJNR. American Journal of Neuroradiology
|
March 30, 2026
Cost-Effectiveness of Adjunctive Middle Meningeal Artery Embolization for Chronic Subdural Hematoma: Secondary Analysis of EMBOLISE
Matthew C Findlay, Gurpreet S Gandhoke, Jason M Davies, et al.
American Journal of Epidemiology
|
April 19, 2011
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people
Gareth J McKay, Giuliana Silvestri, Usha Chakravarthy, et al.
American Journal of Human Genetics
|
March 14, 2017
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies
Mingchu Xu, Yajing Angela Xie, Hana Abouzeid, et al.
NPJ Genomic Medicine
|
April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypes
Ryan E Schmidt, Amy E Pohodich, David Birch, et al.
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of 125
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Showing results (1221-1230 of 1,250) with videos related to
Sort By:
Page
of 125
American Journal of Human Genetics
|
August 27, 2024
Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression
Samantha Malka, Pooja Biswas, Anne-Marie Berry, et al.
Journal of Neurointerventional Surgery
|
August 27, 2020
International experience of mechanical thrombectomy during the COVID-19 pandemic: insights from STAR and ENRG
Sami Al Kasab, Eyad Almallouhi, Ali Alawieh, et al.
Nature Machine Intelligence
|
June 26, 2025
Next-generation phenotyping of inherited retinal diseases from multimodal imaging with Eye2Gene
Nikolas Pontikos, William A Woof, Siying Lin, et al.
Journal of Medicinal Chemistry
|
September 17, 2025
Fragment-Based Discovery and Structure-Led Optimization of MSC778, the First Potent, Selective, and Orally Bioavailable FEN1 Inhibitor
Sam E Mann, Julien Lefranc, Omar Alkhatib, et al.
Nature
|
April 5, 2016
sFRP2 in the aged microenvironment drives melanoma metastasis and therapy resistance
Amanpreet Kaur, Marie R Webster, Katie Marchbank, et al.
The New England Journal of Medicine
|
November 20, 2024
Adjunctive Middle Meningeal Artery Embolization for Subdural Hematoma
Jason M Davies, Jared Knopman, Maxim Mokin, et al.
AJNR. American Journal of Neuroradiology
|
March 30, 2026
Cost-Effectiveness of Adjunctive Middle Meningeal Artery Embolization for Chronic Subdural Hematoma: Secondary Analysis of EMBOLISE
Matthew C Findlay, Gurpreet S Gandhoke, Jason M Davies, et al.
American Journal of Epidemiology
|
April 19, 2011
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people
Gareth J McKay, Giuliana Silvestri, Usha Chakravarthy, et al.
American Journal of Human Genetics
|
March 14, 2017
Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies
Mingchu Xu, Yajing Angela Xie, Hana Abouzeid, et al.
NPJ Genomic Medicine
|
April 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypes
Ryan E Schmidt, Amy E Pohodich, David Birch, et al.
Page
of 125