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The Journal of Urology
|
October 1, 1980
Serum alpha-fetoprotein and human chorionic gonadotropin in patients with seminoma
P H Lange, L E Nochomovitz, J Rosai, et al.
Human Mutation
|
December 22, 2017
Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant
Sarah A Sandaradura, Adam Bournazos, Amali Mallawaarachchi, et al.
Nature
|
March 9, 2018
Corrigendum: Landscape of X chromosome inactivation across human tissues
Taru Tukiainen, Alexandra-Chloé Villani, Angela Yen, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)
|
June 30, 2025
Controversies, consensuses and guidelines on posterior chamber phakic intraocular lens for the correction of myopia and myopic astigmatism in healthy phakic eyes by the Academy of Asia-Pacific Professors of Ophthalmology (AAPPO) and the Asia-Pacific Myopia Society (APMS)
Kenny H W Lai, Xiao Ying Wang, Kelvin H Wan, et al.
Nature
|
August 3, 2022
Transcriptome variation in human tissues revealed by long-read sequencing
Dafni A Glinos, Garrett Garborcauskas, Paul Hoffman, et al.
Ebiomedicine
|
May 13, 2025
An ANGPTL4 inhibitory antibody safely improves lipid profiles in non-human primates
Beryl B Cummings, Page R Bouchard, Mark N Milton, et al.
EMBO Molecular Medicine
|
November 15, 2021
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy
Sandra Donkervoort, Niklas Krause, Mykola Dergai, et al.
Lancet (London, England)
|
May 18, 2025
Safety and efficacy of a novel ANGPTL4 inhibitory antibody for lipid lowering: results from phase 1 and phase 1b/2a clinical studies
Beryl B Cummings, Mark P Joing, Page R Bouchard, et al.
JCI Insight
|
March 22, 2019
A recurrent COL6A1 pseudoexon insertion causes muscular dystrophy and is effectively targeted by splice-correction therapies
Véronique Bolduc, A Reghan Foley, Herimela Solomon-Degefa, et al.
Neurology. Genetics
|
May 12, 2021
WGS and RNA Studies Diagnose Noncoding <i>DMD</i> Variants in Males With High Creatine Kinase
Leigh B Waddell, Samantha J Bryen, Beryl B Cummings, et al.
Page
of 29
Search research articles
Search
Showing results (261-270 of 287) with videos related to
Sort By:
Page
of 29
The Journal of Urology
|
October 1, 1980
Serum alpha-fetoprotein and human chorionic gonadotropin in patients with seminoma
P H Lange, L E Nochomovitz, J Rosai, et al.
Human Mutation
|
December 22, 2017
Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant
Sarah A Sandaradura, Adam Bournazos, Amali Mallawaarachchi, et al.
Nature
|
March 9, 2018
Corrigendum: Landscape of X chromosome inactivation across human tissues
Taru Tukiainen, Alexandra-Chloé Villani, Angela Yen, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)
|
June 30, 2025
Controversies, consensuses and guidelines on posterior chamber phakic intraocular lens for the correction of myopia and myopic astigmatism in healthy phakic eyes by the Academy of Asia-Pacific Professors of Ophthalmology (AAPPO) and the Asia-Pacific Myopia Society (APMS)
Kenny H W Lai, Xiao Ying Wang, Kelvin H Wan, et al.
Nature
|
August 3, 2022
Transcriptome variation in human tissues revealed by long-read sequencing
Dafni A Glinos, Garrett Garborcauskas, Paul Hoffman, et al.
Ebiomedicine
|
May 13, 2025
An ANGPTL4 inhibitory antibody safely improves lipid profiles in non-human primates
Beryl B Cummings, Page R Bouchard, Mark N Milton, et al.
EMBO Molecular Medicine
|
November 15, 2021
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy
Sandra Donkervoort, Niklas Krause, Mykola Dergai, et al.
Lancet (London, England)
|
May 18, 2025
Safety and efficacy of a novel ANGPTL4 inhibitory antibody for lipid lowering: results from phase 1 and phase 1b/2a clinical studies
Beryl B Cummings, Mark P Joing, Page R Bouchard, et al.
JCI Insight
|
March 22, 2019
A recurrent COL6A1 pseudoexon insertion causes muscular dystrophy and is effectively targeted by splice-correction therapies
Véronique Bolduc, A Reghan Foley, Herimela Solomon-Degefa, et al.
Neurology. Genetics
|
May 12, 2021
WGS and RNA Studies Diagnose Noncoding <i>DMD</i> Variants in Males With High Creatine Kinase
Leigh B Waddell, Samantha J Bryen, Beryl B Cummings, et al.
Page
of 29