Literature DB >> 2364541

Hydrocephalus with hop gait (hyh): a new mutation on chromosome 7 in the mouse.

R T Bronson1, P W Lane.   

Abstract

Hydrocephalus with hop gait (hyh) is a new lethal recessive mouse mutation that arose in the C57BL/10J strain at The Jackson Laboratory. It has been mapped to the proximal end of Chromosome 7 close to the Gpi-1 locus. This homozygous mutant is characterized clinically by a domed head and a hopping gait observable at 2 weeks of age and death between 4 and 10 weeks of age. The affected mice have dilated lateral ventricles and a large third ventricular cyst, patent through narrowed rostral cerebral aqueduct, cystic caudal aqueduct and no communication of the aqueduct with the fourth ventricle. The cerebellum has a mild cortical malformation.

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Year:  1990        PMID: 2364541     DOI: 10.1016/0165-3806(90)90073-8

Source DB:  PubMed          Journal:  Brain Res Dev Brain Res        ISSN: 0165-3806


  14 in total

1.  A mutation in the general membrane trafficking machinery and hydrocephaly.

Authors:  Thomas H Söllner
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-02       Impact factor: 11.205

Review 2.  Mouse map of paralogous genes.

Authors:  J H Nadeau; M Kosowsky
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis.

Authors:  Yuanyi Feng; Ming Hui Chen; Ivan P Moskowitz; Ashley M Mendonza; Luis Vidali; Fumihiko Nakamura; David J Kwiatkowski; Christopher A Walsh
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-15       Impact factor: 11.205

Review 4.  Development of brain ventricular system.

Authors:  Vladimir Korzh
Journal:  Cell Mol Life Sci       Date:  2017-08-05       Impact factor: 9.261

5.  Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus.

Authors:  Ming-Jen Lee; Ching-Pang Chang; Yi-Hsin Lee; Yi-Chih Wu; Hsu-Wen Tseng; Yu-Ying Tung; Min-Tzu Wu; Yen-Hui Chen; Lu-Ting Kuo; Dennis Stephenson; Shuen-Iu Hung; Jer-Yuarn Wu; Chen Chang; Yuan-Tsong Chen; Yijuang Chern
Journal:  PLoS One       Date:  2009-11-17       Impact factor: 3.240

6.  The gene for soluble N-ethylmaleimide sensitive factor attachment protein alpha is mutated in hydrocephaly with hop gait (hyh) mice.

Authors:  Hee-Kyung Hong; Aravinda Chakravarti; Joseph S Takahashi
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-30       Impact factor: 11.205

7.  Astrocytes acquire morphological and functional characteristics of ependymal cells following disruption of ependyma in hydrocephalus.

Authors:  Ruth Roales-Buján; Patricia Páez; Montserrat Guerra; Sara Rodríguez; Karin Vío; Ailec Ho-Plagaro; María García-Bonilla; Luis-Manuel Rodríguez-Pérez; María-Dolores Domínguez-Pinos; Esteban-Martín Rodríguez; José-Manuel Pérez-Fígares; Antonio-Jesús Jiménez
Journal:  Acta Neuropathol       Date:  2012-05-11       Impact factor: 17.088

8.  Sperm from hyh mice carrying a point mutation in alphaSNAP have a defect in acrosome reaction.

Authors:  Luis Federico Bátiz; Gerardo A De Blas; Marcela A Michaut; Alfredo R Ramírez; Facundo Rodríguez; Marcelo H Ratto; Cristian Oliver; Claudia N Tomes; Esteban M Rodríguez; Luis S Mayorga
Journal:  PLoS One       Date:  2009-03-23       Impact factor: 3.240

9.  Genetic deletion of afadin causes hydrocephalus by destruction of adherens junctions in radial glial and ependymal cells in the midbrain.

Authors:  Hideaki Yamamoto; Tomohiko Maruo; Takashi Majima; Hiroyoshi Ishizaki; Miki Tanaka-Okamoto; Jun Miyoshi; Kenji Mandai; Yoshimi Takai
Journal:  PLoS One       Date:  2013-11-13       Impact factor: 3.240

10.  Identification of key molecular biomarkers involved in reactive and neurodegenerative processes present in inherited congenital hydrocephalus.

Authors:  Patricia Páez-González; Antonio J Jiménez; Betsaida Ojeda-Pérez; José A Campos-Sandoval; María García-Bonilla; Casimiro Cárdenas-García
Journal:  Fluids Barriers CNS       Date:  2021-07-02
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