New semidominant mutations that affect mouse development
Dominantly acting mutations that produce visible phenotypes are frequently recovered, either during routine maintenance of colonies or from mutagenesis experiments. We have studied 12 dominant mouse mutations that cause a tail dysmorphology, a coat spotting phenotype, or a combination of these. The...
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creator | Bogani, Debora Warr, Nick Elms, Paul Davies, Jennifer Tymowska-Lalanne, Zuzanna Goldsworthy, Michelle Cox, Roger D. Keays, David A. Flint, Jonathan Wilson, Valerie Nolan, Pat Arkell, Ruth |
description | Dominantly acting mutations that produce visible phenotypes are frequently recovered, either during routine maintenance of colonies or from mutagenesis experiments. We have studied 12 dominant mouse mutations that cause a tail dysmorphology, a coat spotting phenotype, or a combination of these. The majority of these mutations act in a semidominant manner with the homozygous state associated with embryonic lethality and a visible phenotype at or before midgestation. The homozygous phenotypes include axis truncation and neural crest cell defects, as may be expected from the heterozygous phenotypes. The majority of mutations, however, also produced other phenotypes that include neural tube closure defects and aberrant heart looping. In one coat spotting mutant the homozygous condition is lethal before neural crest cell production commences. The mutated genes often function in processes additional to those alluded to by the heterozygous phenotype. genesis 40:109–117, 2004. © 2004 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/gene.20071 |
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We have studied 12 dominant mouse mutations that cause a tail dysmorphology, a coat spotting phenotype, or a combination of these. The majority of these mutations act in a semidominant manner with the homozygous state associated with embryonic lethality and a visible phenotype at or before midgestation. The homozygous phenotypes include axis truncation and neural crest cell defects, as may be expected from the heterozygous phenotypes. The majority of mutations, however, also produced other phenotypes that include neural tube closure defects and aberrant heart looping. In one coat spotting mutant the homozygous condition is lethal before neural crest cell production commences. The mutated genes often function in processes additional to those alluded to by the heterozygous phenotype. genesis 40:109–117, 2004. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 1526-954X</identifier><identifier>EISSN: 1526-968X</identifier><identifier>DOI: 10.1002/gene.20071</identifier><identifier>PMID: 15384171</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Alkylating Agents - pharmacology ; Animals ; Animals, Congenic ; Biomarkers ; brachyury ; Chromosome Mapping ; Embryonic Development - genetics ; ENU ; Ethylnitrosourea - pharmacology ; Female ; Genes, Dominant ; Genes, Lethal ; Genetic Markers ; Genome ; Hair Color - genetics ; Haplotypes ; Homozygote ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C3H ; Mice, Mutant Strains ; mouse gastrulation ; Mutagens - pharmacology ; Mutation ; Pax3 ; Polymorphism, Genetic ; Tail - abnormalities ; Wnt3a</subject><ispartof>Genesis (New York, N.Y. : 2000), 2004-10, Vol.40 (2), p.109-117</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4301-b50a47bbca765b0ceb199fe4b974882f0d711314438369ddeb26bc843ff630c53</citedby><cites>FETCH-LOGICAL-c4301-b50a47bbca765b0ceb199fe4b974882f0d711314438369ddeb26bc843ff630c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fgene.20071$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fgene.20071$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15384171$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bogani, Debora</creatorcontrib><creatorcontrib>Warr, Nick</creatorcontrib><creatorcontrib>Elms, Paul</creatorcontrib><creatorcontrib>Davies, Jennifer</creatorcontrib><creatorcontrib>Tymowska-Lalanne, Zuzanna</creatorcontrib><creatorcontrib>Goldsworthy, Michelle</creatorcontrib><creatorcontrib>Cox, Roger D.</creatorcontrib><creatorcontrib>Keays, David A.</creatorcontrib><creatorcontrib>Flint, Jonathan</creatorcontrib><creatorcontrib>Wilson, Valerie</creatorcontrib><creatorcontrib>Nolan, Pat</creatorcontrib><creatorcontrib>Arkell, Ruth</creatorcontrib><title>New semidominant mutations that affect mouse development</title><title>Genesis (New York, N.Y. : 2000)</title><addtitle>Genesis</addtitle><description>Dominantly acting mutations that produce visible phenotypes are frequently recovered, either during routine maintenance of colonies or from mutagenesis experiments. We have studied 12 dominant mouse mutations that cause a tail dysmorphology, a coat spotting phenotype, or a combination of these. The majority of these mutations act in a semidominant manner with the homozygous state associated with embryonic lethality and a visible phenotype at or before midgestation. The homozygous phenotypes include axis truncation and neural crest cell defects, as may be expected from the heterozygous phenotypes. The majority of mutations, however, also produced other phenotypes that include neural tube closure defects and aberrant heart looping. In one coat spotting mutant the homozygous condition is lethal before neural crest cell production commences. The mutated genes often function in processes additional to those alluded to by the heterozygous phenotype. genesis 40:109–117, 2004. © 2004 Wiley‐Liss, Inc.</description><subject>Alkylating Agents - pharmacology</subject><subject>Animals</subject><subject>Animals, Congenic</subject><subject>Biomarkers</subject><subject>brachyury</subject><subject>Chromosome Mapping</subject><subject>Embryonic Development - genetics</subject><subject>ENU</subject><subject>Ethylnitrosourea - pharmacology</subject><subject>Female</subject><subject>Genes, Dominant</subject><subject>Genes, Lethal</subject><subject>Genetic Markers</subject><subject>Genome</subject><subject>Hair Color - genetics</subject><subject>Haplotypes</subject><subject>Homozygote</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C3H</subject><subject>Mice, Mutant Strains</subject><subject>mouse gastrulation</subject><subject>Mutagens - pharmacology</subject><subject>Mutation</subject><subject>Pax3</subject><subject>Polymorphism, Genetic</subject><subject>Tail - abnormalities</subject><subject>Wnt3a</subject><issn>1526-954X</issn><issn>1526-968X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqWw4QNQViyQUuzYTpwlqkpAKgVVQLuz7GQMgTxKnFD696SkhR2rGY3OPRpdhE4JHhKMvcsXKGDoYRyQPdQn3PPd0BeL_d3O2aKHjqx9wxhz4XmHqEc4FYwEpI_EFFaOhTxNyjwtVFE7eVOrOi0L69SvqnaUMRC317Kx4CTwCVm5zKGoj9GBUZmFk-0coKfr8ePoxp3cR7ejq4kbM4qJqzlWLNA6VoHPNY5BkzA0wHQYMCE8g5OAEEoYo4L6YZKA9nwdC0aN8SmOOR2g8867rMqPBmwt89TGkGWqgPYn6WHGW5NowYsOjKvS2gqMXFZprqq1JFhuepKbnuRPTy18trU2OofkD90W0wKkA1ZpBut_VDIaT8c7qdtlUlvD129GVe_SD2jA5XwayXA2e17czSP5QL8BbXiCDw</recordid><startdate>200410</startdate><enddate>200410</enddate><creator>Bogani, Debora</creator><creator>Warr, Nick</creator><creator>Elms, Paul</creator><creator>Davies, Jennifer</creator><creator>Tymowska-Lalanne, Zuzanna</creator><creator>Goldsworthy, Michelle</creator><creator>Cox, Roger D.</creator><creator>Keays, David A.</creator><creator>Flint, Jonathan</creator><creator>Wilson, Valerie</creator><creator>Nolan, Pat</creator><creator>Arkell, Ruth</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>200410</creationdate><title>New semidominant mutations that affect mouse development</title><author>Bogani, Debora ; Warr, Nick ; Elms, Paul ; Davies, Jennifer ; Tymowska-Lalanne, Zuzanna ; Goldsworthy, Michelle ; Cox, Roger D. ; Keays, David A. ; Flint, Jonathan ; Wilson, Valerie ; Nolan, Pat ; Arkell, Ruth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4301-b50a47bbca765b0ceb199fe4b974882f0d711314438369ddeb26bc843ff630c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Alkylating Agents - pharmacology</topic><topic>Animals</topic><topic>Animals, Congenic</topic><topic>Biomarkers</topic><topic>brachyury</topic><topic>Chromosome Mapping</topic><topic>Embryonic Development - genetics</topic><topic>ENU</topic><topic>Ethylnitrosourea - pharmacology</topic><topic>Female</topic><topic>Genes, Dominant</topic><topic>Genes, Lethal</topic><topic>Genetic Markers</topic><topic>Genome</topic><topic>Hair Color - genetics</topic><topic>Haplotypes</topic><topic>Homozygote</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C3H</topic><topic>Mice, Mutant Strains</topic><topic>mouse gastrulation</topic><topic>Mutagens - pharmacology</topic><topic>Mutation</topic><topic>Pax3</topic><topic>Polymorphism, Genetic</topic><topic>Tail - abnormalities</topic><topic>Wnt3a</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bogani, Debora</creatorcontrib><creatorcontrib>Warr, Nick</creatorcontrib><creatorcontrib>Elms, Paul</creatorcontrib><creatorcontrib>Davies, Jennifer</creatorcontrib><creatorcontrib>Tymowska-Lalanne, Zuzanna</creatorcontrib><creatorcontrib>Goldsworthy, Michelle</creatorcontrib><creatorcontrib>Cox, Roger D.</creatorcontrib><creatorcontrib>Keays, David A.</creatorcontrib><creatorcontrib>Flint, Jonathan</creatorcontrib><creatorcontrib>Wilson, Valerie</creatorcontrib><creatorcontrib>Nolan, Pat</creatorcontrib><creatorcontrib>Arkell, Ruth</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Genesis (New York, N.Y. : 2000)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bogani, Debora</au><au>Warr, Nick</au><au>Elms, Paul</au><au>Davies, Jennifer</au><au>Tymowska-Lalanne, Zuzanna</au><au>Goldsworthy, Michelle</au><au>Cox, Roger D.</au><au>Keays, David A.</au><au>Flint, Jonathan</au><au>Wilson, Valerie</au><au>Nolan, Pat</au><au>Arkell, Ruth</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New semidominant mutations that affect mouse development</atitle><jtitle>Genesis (New York, N.Y. : 2000)</jtitle><addtitle>Genesis</addtitle><date>2004-10</date><risdate>2004</risdate><volume>40</volume><issue>2</issue><spage>109</spage><epage>117</epage><pages>109-117</pages><issn>1526-954X</issn><eissn>1526-968X</eissn><abstract>Dominantly acting mutations that produce visible phenotypes are frequently recovered, either during routine maintenance of colonies or from mutagenesis experiments. We have studied 12 dominant mouse mutations that cause a tail dysmorphology, a coat spotting phenotype, or a combination of these. The majority of these mutations act in a semidominant manner with the homozygous state associated with embryonic lethality and a visible phenotype at or before midgestation. The homozygous phenotypes include axis truncation and neural crest cell defects, as may be expected from the heterozygous phenotypes. The majority of mutations, however, also produced other phenotypes that include neural tube closure defects and aberrant heart looping. In one coat spotting mutant the homozygous condition is lethal before neural crest cell production commences. The mutated genes often function in processes additional to those alluded to by the heterozygous phenotype. genesis 40:109–117, 2004. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15384171</pmid><doi>10.1002/gene.20071</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alkylating Agents - pharmacology Animals Animals, Congenic Biomarkers brachyury Chromosome Mapping Embryonic Development - genetics ENU Ethylnitrosourea - pharmacology Female Genes, Dominant Genes, Lethal Genetic Markers Genome Hair Color - genetics Haplotypes Homozygote Male Mice Mice, Inbred BALB C Mice, Inbred C3H Mice, Mutant Strains mouse gastrulation Mutagens - pharmacology Mutation Pax3 Polymorphism, Genetic Tail - abnormalities Wnt3a |
title | New semidominant mutations that affect mouse development |
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