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Erwin Pauws

Showing results (21-30 of 28) with videos related to

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Human Molecular Genetics|August 4, 2009
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypesErwin Pauws, Aya Hoshino, Lucy Bentley, et al.
Disease Models & Mechanisms|March 18, 2026
Chiari II brain malformation is secondary to open spina bifidaMaryam Clark, Timothy J Edwards, Dawn Savery, et al.
American Journal of Human Genetics|September 12, 2007
TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repressionArtemisia M Andreou, Erwin Pauws, Marius C Jones, et al.
Proceedings. Biological Sciences|August 19, 2025
Unravelling the difference in craniofacial morphology of Yucatan miniature and standard pigs during postnatal ontogenyCe Liang, Tengyang Qiu, Arsalan Marghoub, et al.
Disease Models & Mechanisms|March 23, 2013
Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screeningDavid Adams, Richard Baldock, Shoumo Bhattacharya, et al.
Journal of Anatomy|August 3, 2024
Cranial bone microarchitecture in a mouse model for syndromic craniosynostosisSara Ajami, Zoe Van den Dam, Julia Hut, et al.
American Journal of Human Genetics|September 5, 2015
Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning DisabilityStephen R F Twigg, Jennifer Forecki, Jacqueline A C Goos, et al.
The EMBO Journal|May 17, 2018
Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosisPietro Fratta, Prasanth Sivakumar, Jack Humphrey, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Human Molecular Genetics|August 4, 2009
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypesErwin Pauws, Aya Hoshino, Lucy Bentley, et al.
Disease Models & Mechanisms|March 18, 2026
Chiari II brain malformation is secondary to open spina bifidaMaryam Clark, Timothy J Edwards, Dawn Savery, et al.
American Journal of Human Genetics|September 12, 2007
TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repressionArtemisia M Andreou, Erwin Pauws, Marius C Jones, et al.
Proceedings. Biological Sciences|August 19, 2025
Unravelling the difference in craniofacial morphology of Yucatan miniature and standard pigs during postnatal ontogenyCe Liang, Tengyang Qiu, Arsalan Marghoub, et al.
Disease Models & Mechanisms|March 23, 2013
Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screeningDavid Adams, Richard Baldock, Shoumo Bhattacharya, et al.
Journal of Anatomy|August 3, 2024
Cranial bone microarchitecture in a mouse model for syndromic craniosynostosisSara Ajami, Zoe Van den Dam, Julia Hut, et al.
American Journal of Human Genetics|September 5, 2015
Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning DisabilityStephen R F Twigg, Jennifer Forecki, Jacqueline A C Goos, et al.
The EMBO Journal|May 17, 2018
Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosisPietro Fratta, Prasanth Sivakumar, Jack Humphrey, et al.
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