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Human Molecular Genetics
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November 7, 2022
A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia
Abhishek Anil Dubey, Magdalena Krygier, Natalia A Szulc, et al.
Stem Cell Research & Therapy
|
November 15, 2023
Bright ferritin for long-term MR imaging of human embryonic stem cells
Keyu Zhuang, Rocco Romagnuolo, Tamilla Sadikov Valdman, et al.
The EMBO Journal
|
June 28, 2022
A heterotypic assembly mechanism regulates CHIP E3 ligase activity
Aniruddha Das, Pankaj Thapa, Ulises Santiago, et al.
Plos Genetics
|
August 25, 2025
Tissue-specific consequences of tag fusions on protein expression in transgenic mice
Gillian C A Taylor, Lewis Macdonald, Natalia A Szulc, et al.
Nature Communications
|
March 25, 2022
UBR4/POE facilitates secretory trafficking to maintain circadian clock synchrony
Sara Hegazi, Arthur H Cheng, Joshua J Krupp, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 65) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 65 results.
Human Molecular Genetics
|
November 7, 2022
A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia
Abhishek Anil Dubey, Magdalena Krygier, Natalia A Szulc, et al.
Stem Cell Research & Therapy
|
November 15, 2023
Bright ferritin for long-term MR imaging of human embryonic stem cells
Keyu Zhuang, Rocco Romagnuolo, Tamilla Sadikov Valdman, et al.
The EMBO Journal
|
June 28, 2022
A heterotypic assembly mechanism regulates CHIP E3 ligase activity
Aniruddha Das, Pankaj Thapa, Ulises Santiago, et al.
Plos Genetics
|
August 25, 2025
Tissue-specific consequences of tag fusions on protein expression in transgenic mice
Gillian C A Taylor, Lewis Macdonald, Natalia A Szulc, et al.
Nature Communications
|
March 25, 2022
UBR4/POE facilitates secretory trafficking to maintain circadian clock synchrony
Sara Hegazi, Arthur H Cheng, Joshua J Krupp, et al.
Page
of 7