Quantitative Morphologic Analysis of Cranial Vault in Twist1 +/− Mice: Implications in Craniosynostosis

• 資料種別: 記事
• タイトル: Quantitative Morphologic Analysis of Cranial Vault in Twist1 +/− Mice: Implications in Craniosynostosis
• 著者標目: Takashi Nuri; Masato Ota; Koichi Ueda; Sachiko Iseki
• 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: Surgery
• 対象利用者: 一般
• DOI: 10.1097/prs.0000000000008665
• 作成日（W3CDTF）: 2021-12-22
• 関連情報（URI）: https://journals.lww.com/10.1097/PRS.0000000000008665
• 参照: Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis; https://cir.nii.ac.jp/crid/1360298754812496640
• 参照: Pivotal role of Twist in skeletal biology and pathology; https://cir.nii.ac.jp/crid/1360011145251851136; Molecular Genetic Advances in Understanding Craniosynostosis; https://cir.nii.ac.jp/crid/1360017285779966976; Mutations within or upstream of the basic helix–loop–helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome; https://cir.nii.ac.jp/crid/1360017287278144640; Craniosynostosis: genes and mechanisms; https://cir.nii.ac.jp/crid/1360292619792581760; Recurrence of Synostosis following Surgical Repair of Craniosynostosis; https://cir.nii.ac.jp/crid/1360298761569081600; Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies; https://cir.nii.ac.jp/crid/1360574095180920320; Clinical and Genetic Analysis of Patients with Saethre-Chotzen Syndrome; https://cir.nii.ac.jp/crid/1360574095402454912; Fronto-orbital re-operation in craniosynostosis; https://cir.nii.ac.jp/crid/1360580236113566080; Increased Intracranial Pressure After Coronal Suturectomy in Craniosynostotic Rabbits; https://cir.nii.ac.jp/crid/1360580238511340800; Craniosynostosis in <i>Twist</i> heterozygous mice: A model for Saethre‐Chotzen syndrome; https://cir.nii.ac.jp/crid/1360861709786038656; Craniofacial Shape Variation in <i>Twist1^+/−</i> Mutant Mice; https://cir.nii.ac.jp/crid/1360861709786040064; Craniofacial abnormalities in a murine model of Saethre-Chotzen Syndrome; https://cir.nii.ac.jp/crid/1360861711579897472; The pathogenesis of craniosynostosis in the fetus; https://cir.nii.ac.jp/crid/1360861711581606272; The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases; https://cir.nii.ac.jp/crid/1360861714469993344; Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome; https://cir.nii.ac.jp/crid/1360861714471218560; Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome; https://cir.nii.ac.jp/crid/1361137044119496576; Twenty-Year Experience with Early Surgery for Craniosynostosis; https://cir.nii.ac.jp/crid/1361137044537429120; twist is required in head mesenchyme for cranial neural tube morphogenesis.; https://cir.nii.ac.jp/crid/1361137045841388416; Twist is required for establishment of the mouse coronal suture; https://cir.nii.ac.jp/crid/1361137046255305472; The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome; https://cir.nii.ac.jp/crid/1361418520936899712; Interrelationship of Cranial Suture Fusion, Basicranial Development, and Resynostosis Following Suturectomy in Twist1+/− Mice, a Murine Model of Saethre-Chotzen Syndrome; https://cir.nii.ac.jp/crid/1361418521378311680; Saethre-Chotzen syndrome.; https://cir.nii.ac.jp/crid/1361699995536478720; Parallels of craniofacial maldevelopment in down syndrome and Ts65Dn mice; https://cir.nii.ac.jp/crid/1362262944462897280; Genetic advances in craniosynostosis; https://cir.nii.ac.jp/crid/1362544420074075904; Reoperation for Intracranial Hypertension in TWIST1-Confirmed Saethre-Chotzen Syndrome: A 15-Year Review; https://cir.nii.ac.jp/crid/1362825893359055360; Mutations of the TWIST gene in the Saethre-Chotzene syndrome; https://cir.nii.ac.jp/crid/1362825894120153728; The Craniofacial Phenotype of the Crouzon Mouse: Analysis of a Model for Syndromic Craniosynostosis Using Three-Dimensional MicroCT; https://cir.nii.ac.jp/crid/1363388845736091264; Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome; https://cir.nii.ac.jp/crid/1363670318219892608; Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations; https://cir.nii.ac.jp/crid/1363670318858064128; A population‐based study of craniosynostosis in metropolitan Atlanta, 1989–2003; https://cir.nii.ac.jp/crid/1363670320035224960; Clinical genetics of craniosynostosis; https://cir.nii.ac.jp/crid/1363951793248004736; Craniosynostosis.; https://cir.nii.ac.jp/crid/1370298754843755405
• 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; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja

• 要約等: <jats:sec> <jats:title>Background:</jats:title> <jats:p>The haploinsufficiency in the <jats:italic toggle="yes">TWIST1</jats:i...