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Quantitative Morphologic Analysis of Cranial Vault in Twist1 +/− Mice: Implications in Craniosynostosis
- 資料種別
- 記事
- 著者
- Takashi Nuriほか
- 出版者
- Ovid Technologies (Wolters Kluwer Health)
- 出版年
- 2021-12-21
- 資料形態
- デジタル
- 掲載誌名
- Plastic & Reconstructive Surgery 149 1
- 掲載ページ
- p.28e-37e
資料詳細
要約等:
- <jats:sec> <jats:title>Background:</jats:title> <jats:p>The haploinsufficiency in the <jats:italic toggle="yes">TWIST1</jats:i...
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デジタル
- 資料種別
- 記事
- 出版年月日等
- 2021-12-21
- 出版年(W3CDTF)
- 2021-12-21
- タイトル(掲載誌)
- Plastic & Reconstructive Surgery
- 巻号年月日等(掲載誌)
- 149 1
- 掲載巻
- 149
- 掲載号
- 1
- 掲載ページ
- 28e-37e
- 掲載年月日(W3CDTF)
- 2021-12-21
- ISSN(掲載誌)
- 00321052
- 出版事項(掲載誌)
- Ovid Technologies (Wolters Kluwer Health)
- 件名標目
- 対象利用者
- 一般
- DOI
- 10.1097/prs.0000000000008665
- 作成日(W3CDTF)
- 2021-12-22
- 参照
- Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis
- 参照
- Pivotal role of Twist in skeletal biology and pathologyMolecular Genetic Advances in Understanding CraniosynostosisMutations within or upstream of the basic helix–loop–helix domain of the TWIST gene are specific to Saethre-Chotzen syndromeCraniosynostosis: genes and mechanismsRecurrence of Synostosis following Surgical Repair of CraniosynostosisGrowth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studiesClinical and Genetic Analysis of Patients with Saethre-Chotzen SyndromeFronto-orbital re-operation in craniosynostosisIncreased Intracranial Pressure After Coronal Suturectomy in Craniosynostotic RabbitsCraniosynostosis in <i>Twist</i> heterozygous mice: A model for Saethre‐Chotzen syndromeCraniofacial Shape Variation in <i>Twist1<sup>+/−</sup></i> Mutant MiceCraniofacial abnormalities in a murine model of Saethre-Chotzen SyndromeThe pathogenesis of craniosynostosis in the fetusThe TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic casesAltered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndromeSaethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndromeTwenty-Year Experience with Early Surgery for Craniosynostosistwist is required in head mesenchyme for cranial neural tube morphogenesis.Twist is required for establishment of the mouse coronal sutureThe variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndromeInterrelationship of Cranial Suture Fusion, Basicranial Development, and Resynostosis Following Suturectomy in Twist1+/− Mice, a Murine Model of Saethre-Chotzen SyndromeSaethre-Chotzen syndrome.Parallels of craniofacial maldevelopment in down syndrome and Ts65Dn miceGenetic advances in craniosynostosisReoperation for Intracranial Hypertension in TWIST1-Confirmed Saethre-Chotzen Syndrome: A 15-Year ReviewMutations of the TWIST gene in the Saethre-Chotzene syndromeThe Craniofacial Phenotype of the Crouzon Mouse: Analysis of a Model for Syndromic Craniosynostosis Using Three-Dimensional MicroCTMutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndromeGenetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR MutationsA population‐based study of craniosynostosis in metropolitan Atlanta, 1989–2003Clinical genetics of craniosynostosisCraniosynostosis.
- 連携機関・データベース
- 国立情報学研究所 : CiNii Research
- 提供元機関・データベース
- Crossref科学研究費助成事業データベースCrossref