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Irene E Zohn

Showing results (31-40 of 35) with videos related to

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Frontiers in Neurology|February 22, 2020
Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion SyndromeLauren Welby, Hailey Caudill, Gelila Yitsege, et al.
Birth Defects Research|May 21, 2020
Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndromeGelila Yitsege, Bethany A Stokes, Julia A Sabatino, et al.
The Journal of Biological Chemistry|January 2, 2013
HectD1 E3 ligase modifies adenomatous polyposis coli (APC) with polyubiquitin to promote the APC-axin interactionHoanh Tran, Daisy Bustos, Ronald Yeh, et al.
Nature Genetics|December 7, 2010
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formationAnita Becker-Heck, Irene E Zohn, Noriko Okabe, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Frontiers in Neurology|February 22, 2020
Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion SyndromeLauren Welby, Hailey Caudill, Gelila Yitsege, et al.
Birth Defects Research|May 21, 2020
Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndromeGelila Yitsege, Bethany A Stokes, Julia A Sabatino, et al.
The Journal of Biological Chemistry|January 2, 2013
HectD1 E3 ligase modifies adenomatous polyposis coli (APC) with polyubiquitin to promote the APC-axin interactionHoanh Tran, Daisy Bustos, Ronald Yeh, et al.
Nature Genetics|December 7, 2010
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formationAnita Becker-Heck, Irene E Zohn, Noriko Okabe, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Pageof 4