![The relationship between ventricular dilatation, neuropathological and neurobehavioural changes in hydrocephalic rats | Fluids and Barriers of the CNS | Full Text The relationship between ventricular dilatation, neuropathological and neurobehavioural changes in hydrocephalic rats | Fluids and Barriers of the CNS | Full Text](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2F2045-8118-9-19/MediaObjects/12987_2012_Article_40_Fig1_HTML.jpg)
The relationship between ventricular dilatation, neuropathological and neurobehavioural changes in hydrocephalic rats | Fluids and Barriers of the CNS | Full Text
![Hydrocephalus and the Accidental Transgene; Redox RNA; To Be a Bee, but He or She? | The Scientist Magazine® Hydrocephalus and the Accidental Transgene; Redox RNA; To Be a Bee, but He or She? | The Scientist Magazine®](http://images.the-scientist.com/content/figures/images/yr2003/sep22/mice.jpg)
Hydrocephalus and the Accidental Transgene; Redox RNA; To Be a Bee, but He or She? | The Scientist Magazine®
Junctional Adhesion Molecule (JAM)-C Deficient C57BL/6 Mice Develop a Severe Hydrocephalus | PLOS ONE
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Nuclear Factor κB Activation Impairs Ependymal Ciliogenesis and Links Neuroinflammation to Hydrocephalus Formation | Journal of Neuroscience
![Murine MPDZ‐linked hydrocephalus is caused by hyperpermeability of the choroid plexus | EMBO Molecular Medicine Murine MPDZ‐linked hydrocephalus is caused by hyperpermeability of the choroid plexus | EMBO Molecular Medicine](https://www.embopress.org/cms/asset/daee1188-ca80-4c8f-9c94-f019a27b43fa/emmm201809540-fig-0001-m.png)
Murine MPDZ‐linked hydrocephalus is caused by hyperpermeability of the choroid plexus | EMBO Molecular Medicine
![Tg737 orpk mutant mice develop hydrocephalus. (A) Comparison of lateral... | Download Scientific Diagram Tg737 orpk mutant mice develop hydrocephalus. (A) Comparison of lateral... | Download Scientific Diagram](https://www.researchgate.net/publication/7484533/figure/fig1/AS:394419460165634@1471048335853/Tg737-orpk-mutant-mice-develop-hydrocephalus-A-Comparison-of-lateral-views-of.png)
Tg737 orpk mutant mice develop hydrocephalus. (A) Comparison of lateral... | Download Scientific Diagram
![Multigenic factors associated with a hydrocephalus-like phenotype found in inter-subspecific consomic mouse strains | Mammalian Genome Multigenic factors associated with a hydrocephalus-like phenotype found in inter-subspecific consomic mouse strains | Mammalian Genome](https://media.springernature.com/m685/springer-static/image/art%3A10.1007%2Fs00335-008-9112-2/MediaObjects/335_2008_9112_Fig1_HTML.jpg)
Multigenic factors associated with a hydrocephalus-like phenotype found in inter-subspecific consomic mouse strains | Mammalian Genome
![JCI Insight - MT1-MMP deficiency leads to defective ependymal cell maturation, impaired ciliogenesis, and hydrocephalus JCI Insight - MT1-MMP deficiency leads to defective ependymal cell maturation, impaired ciliogenesis, and hydrocephalus](https://df6sxcketz7bb.cloudfront.net/manuscripts/132000/132782/medium/jci.insight.132782.f1.jpg)
JCI Insight - MT1-MMP deficiency leads to defective ependymal cell maturation, impaired ciliogenesis, and hydrocephalus
![Neonatal hydrocephalus is a result of a block in folate handling and metabolism involving 10‐formyltetrahydrofolate dehydrogenase - Naz - 2016 - Journal of Neurochemistry - Wiley Online Library Neonatal hydrocephalus is a result of a block in folate handling and metabolism involving 10‐formyltetrahydrofolate dehydrogenase - Naz - 2016 - Journal of Neurochemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/78ef7d8e-45c6-42d0-83e3-941c298f268c/jnc13686-fig-0001-m.jpg)
Neonatal hydrocephalus is a result of a block in folate handling and metabolism involving 10‐formyltetrahydrofolate dehydrogenase - Naz - 2016 - Journal of Neurochemistry - Wiley Online Library
![Hydrocephalus caused by conditional ablation of the Pten or beta-catenin gene | Fluids and Barriers of the CNS | Full Text Hydrocephalus caused by conditional ablation of the Pten or beta-catenin gene | Fluids and Barriers of the CNS | Full Text](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2F1743-8454-5-16/MediaObjects/12987_2008_Article_297_Fig1_HTML.jpg)
Hydrocephalus caused by conditional ablation of the Pten or beta-catenin gene | Fluids and Barriers of the CNS | Full Text
Congenital Hydrocephalus and Abnormal Subcommissural Organ Development in Sox3 Transgenic Mice | PLOS ONE
Hydrocephalus in bgh mice. A) Gross hydrocephalus in bgh homozygote. B)... | Download Scientific Diagram
![Sicily has congenital hydrocephalus, but it doesn't stop her from living her best rat life. She is already 10 months old and going strong! 💛🐀💛 : r/aww Sicily has congenital hydrocephalus, but it doesn't stop her from living her best rat life. She is already 10 months old and going strong! 💛🐀💛 : r/aww](https://i.redd.it/fi337l10n5671.jpg)
Sicily has congenital hydrocephalus, but it doesn't stop her from living her best rat life. She is already 10 months old and going strong! 💛🐀💛 : r/aww
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SNX27 Deletion Causes Hydrocephalus by Impairing Ependymal Cell Differentiation and Ciliogenesis | Journal of Neuroscience
![Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS](https://www.pnas.org/cms/10.1073/pnas.1219995110/asset/1c066bf0-0a26-4be1-a6c0-67dae1774ae1/assets/graphic/pnas.1219995110fig02.jpeg)
Genetic deletion of Rnd3 results in aqueductal stenosis leading to hydrocephalus through up-regulation of Notch signaling | PNAS
![Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development | Semantic Scholar Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/c4ff7f8686ff68635e74d49c2a4f3cbdd992acd7/2-Figure1-1.png)
Loss of Fyn tyrosine kinase on the C57BL/6 genetic background causes hydrocephalus with defects in oligodendrocyte development | Semantic Scholar
![Figure 1 from The dynamics of brain and cerebrospinal fluid growth in normal versus hydrocephalic mice. | Semantic Scholar Figure 1 from The dynamics of brain and cerebrospinal fluid growth in normal versus hydrocephalic mice. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a631bddbd8ca6dbd2d2430e12b73365e6e311d65/3-Figure1-1.png)
Figure 1 from The dynamics of brain and cerebrospinal fluid growth in normal versus hydrocephalic mice. | Semantic Scholar
![Mdnah5 –/– mice have hydrocephalus and growth retardation. (A) Mdnah5... | Download Scientific Diagram Mdnah5 –/– mice have hydrocephalus and growth retardation. (A) Mdnah5... | Download Scientific Diagram](https://www.researchgate.net/publication/277441576/figure/fig3/AS:388351459905539@1469601611221/Mdnah5--mice-have-hydrocephalus-and-growth-retardation-A-Mdnah5--mouse-bottom.png)
Mdnah5 –/– mice have hydrocephalus and growth retardation. (A) Mdnah5... | Download Scientific Diagram
Junctional Adhesion Molecule (JAM)-C Deficient C57BL/6 Mice Develop a Severe Hydrocephalus | PLOS ONE
![Disruption of Wave-associated Rac GTPase-activating Protein (Wrp) Leads to Abnormal Adult Neural Progenitor Migration Associated with Hydrocephalus - ScienceDirect Disruption of Wave-associated Rac GTPase-activating Protein (Wrp) Leads to Abnormal Adult Neural Progenitor Migration Associated with Hydrocephalus - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0021925820623870-gr1.jpg)
Disruption of Wave-associated Rac GTPase-activating Protein (Wrp) Leads to Abnormal Adult Neural Progenitor Migration Associated with Hydrocephalus - ScienceDirect
![New mechanism driving cortical gyrification and hydrocephalus found in mice suggests scope for novel therapy New mechanism driving cortical gyrification and hydrocephalus found in mice suggests scope for novel therapy](https://scx2.b-cdn.net/gfx/news/hires/2019/5df228f9f15b9.jpg)
New mechanism driving cortical gyrification and hydrocephalus found in mice suggests scope for novel therapy
![Loss of Rsph9 causes neonatal hydrocephalus with abnormal development of motile cilia in mice | Scientific Reports Loss of Rsph9 causes neonatal hydrocephalus with abnormal development of motile cilia in mice | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-020-69447-4/MediaObjects/41598_2020_69447_Fig2_HTML.png)