<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(14)</volume><submitter>Thumkeo D</submitter><pubmed_abstract>Rho-associated kinase (ROCK), including the ROCK-I and ROCK-II isoforms, is a protein kinase involved in signaling from Rho to actin cytoskeleton. However, in vivo functions of each ROCK isoform remain largely unknown. We generated mice deficient in ROCK-II by gene targeting. ROCK-II(-/-) embryos were found at the expected Mendelian frequency until 13.5 days postcoitum, but approximately 90% died thereafter in utero. ROCK-II(-/-) mice of both genders that survived were born runts, subsequently developed without gross abnormality, and were fertile. Whole-mount staining for a knocked-in lacZ reporter gene revealed that ROCK-II was highly expressed in the labyrinth layer of the placenta. Disruption of architecture and extensive thrombus formation were found in the labyrinth layer of ROCK-II(-</pubmed_abstract><journal>Molecular and cellular biology</journal><pagination>5043-55</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC162229</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Targeted disruption of the mouse rho-associated kinase 2 gene results in intrauterine growth retardation and fetal death.</pubmed_title><pmcid>PMC162229</pmcid><pubmed_authors>Hirose M</pubmed_authors><pubmed_authors>Narumiya S</pubmed_authors><pubmed_authors>Keel J</pubmed_authors><pubmed_authors>Nonomura K</pubmed_authors><pubmed_authors>Thumkeo D</pubmed_authors><pubmed_authors>Oshima M</pubmed_authors><pubmed_authors>Ishizaki T</pubmed_authors><pubmed_authors>Oshima H</pubmed_authors><pubmed_authors>Taketo MM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeted disruption of the mouse rho-associated kinase 2 gene results in intrauterine growth retardation and fetal death.</name><description>Rho-associated kinase (ROCK), including the ROCK-I and ROCK-II isoforms, is a protein kinase involved in signaling from Rho to actin cytoskeleton. However, in vivo functions of each ROCK isoform remain largely unknown. We generated mice deficient in ROCK-II by gene targeting. ROCK-II(-/-) embryos were found at the expected Mendelian frequency until 13.5 days postcoitum, but approximately 90% died thereafter in utero. ROCK-II(-/-) mice of both genders that survived were born runts, subsequently developed without gross abnormality, and were fertile. Whole-mount staining for a knocked-in lacZ reporter gene revealed that ROCK-II was highly expressed in the labyrinth layer of the placenta. Disruption of architecture and extensive thrombus formation were found in the labyrinth layer of ROCK-II(-</description><dates><release>2003-01-01T00:00:00Z</release><publication>2003 Jul</publication><modification>2025-04-19T08:16:13.196Z</modification><creation>2020-11-07T10:18:27Z</creation></dates><accession>S-EPMC162229</accession><cross_references><pubmed>12832488</pubmed><doi>10.1128/MCB.23.14.5043-5055.2003</doi><doi>10.1128/mcb.23.14.5043-5055.2003</doi></cross_references></HashMap>