Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Anatomy Item Literature (14955) Expression Attributions Wiki
XB-ANAT-468

Papers associated with whole organism (and pycr1)

Limit to papers also referencing gene:
Show all whole organism papers
???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

CRISPR-SID: Identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mapping., Naert T., Proc Natl Acad Sci U S A. November 23, 2021; 118 (47):                             

A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit., Manes G., PLoS One. January 1, 2014; 9 (4): e95768.            

Mutations in PYCR1 cause cutis laxa with progeroid features., Reversade B., Nat Genet. September 1, 2009; 41 (9): 1016-21.        

p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development., Keren A., Dev Biol. December 1, 2005; 288 (1): 73-86.              

???pagination.result.page??? 1