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Molecular genetic advances in understanding craniosynostosis.

作者信息

Robin N H

机构信息

Department of Genetics, Case Western Reserve University School of Medicine, University Hospitals of Cleveland, Ohio, USA.

出版信息

Plast Reconstr Surg. 1999 Mar;103(3):1060-70.

PMID:10077104
Abstract
摘要

相似文献

1
Molecular genetic advances in understanding craniosynostosis.理解颅缝早闭的分子遗传学进展。
Plast Reconstr Surg. 1999 Mar;103(3):1060-70.
2
Genetics of craniosynostosis.颅缝早闭的遗传学
Semin Pediatr Neurol. 2007 Sep;14(3):150-61. doi: 10.1016/j.spen.2007.08.008.
3
Craniosynostosis syndromes: from genes to premature fusion of skull bones.颅缝早闭综合征：从基因到颅骨过早融合
Mol Genet Metab. 1999 Oct;68(2):139-51. doi: 10.1006/mgme.1999.2915.
4
Craniosynostosis with tracheal sleeve: a patient with Pfeiffer syndrome, tracheal sleeve and additional malformations in whom an FGFR2 mutation was found.颅骨缝早闭合并气管套状狭窄：一名患有 Pfeiffer 综合征、气管套状狭窄及其他畸形且发现 FGFR2 基因突变的患者。
Clin Dysmorphol. 2003 Jul;12(3):209. doi: 10.1097/01.mcd.0000080414.95344.ae.
5
Craniosynostosis: from a clinical description to an understanding of bone formation of the skull.
Childs Nerv Syst. 1999 Nov;15(11-12):676-80. doi: 10.1007/s003810050457.
6
Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.成纤维细胞生长因子受体3基因Pro250Arg突变所致的家族性颅缝早闭
Ulster Med J. 2001 May;70(1):47-50.
7
Craniosynostosis and skeletal dysplasias: fibroblast growth factor receptor defects.
Proc Assoc Am Physicians. 1996 Jan;108(1):19-24.
8
The molecular pathology of syndromic craniosynostosis.综合征性颅缝早闭的分子病理学
Mol Med Today. 1995 Dec;1(9):432-7. doi: 10.1016/s1357-4310(95)90837-4.
9
Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations.与Apert综合征无关的颅缝早闭患者的表型多样性：成纤维细胞生长因子受体基因突变的作用
J Neurosurg. 2005 Jan;102(1 Suppl):23-30. doi: 10.3171/ped.2005.102.1.0023.
10
[Etiological and pathogenetic mechanisms in development of craniosynostoses in children].
Arkh Patol. 2003 May-Jun;65(3):54-8.

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Sfrp4 expression in thyroxine treated calvarial cells.甲状腺素处理的颅骨细胞中 Sfrp4 的表达。
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2
Pharmacological exposures may precipitate craniosynostosis through targeted stem cell depletion.药物暴露可能通过靶向干细胞耗竭而引发颅缝早闭。
Stem Cell Res. 2019 Oct;40:101528. doi: 10.1016/j.scr.2019.101528. Epub 2019 Aug 6.
3
Effects of thyroxine exposure on the Twist 1 +/- phenotype: A test of gene-environment interaction modeling for craniosynostosis.
甲状腺素暴露对Twist 1+/-表型的影响：颅缝早闭基因-环境相互作用模型的一项测试
Birth Defects Res A Clin Mol Teratol. 2016 Oct;106(10):803-813. doi: 10.1002/bdra.23543. Epub 2016 Jul 20.
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Executive Function and Adaptive Behavior in Muenke Syndrome.孟基综合征中的执行功能与适应性行为
J Pediatr. 2015 Aug;167(2):428-34. doi: 10.1016/j.jpeds.2015.04.080. Epub 2015 May 28.
5
Osteoprotegerin deficiency results in disruption of posterofrontal suture closure in mice: implications in nonsyndromic craniosynostosis.骨保护素缺乏导致小鼠额后缝闭合中断：对非综合征性颅缝早闭的影响。
Plast Reconstr Surg. 2015 Jun;135(6):990e-999e. doi: 10.1097/PRS.0000000000001284.
6
Talocalcaneal coalition in Muenke syndrome: report of a patient, review of the literature in FGFR-related craniosynostoses, and consideration of mechanism.Muenke 综合征中的跟距骨桥：1 例患者报告，FGFR 相关颅缝早闭症文献复习及发病机制探讨
Am J Med Genet A. 2013 Mar;161A(3):453-60. doi: 10.1002/ajmg.a.35233. Epub 2013 Feb 1.
7
Rapid re-synostosis following suturectomy in pediatric mice is age and location dependent.小儿缝线切除术后快速再颅缝融合与年龄和部位有关。
Bone. 2013 Mar;53(1):284-93. doi: 10.1016/j.bone.2012.11.019. Epub 2012 Nov 28.
8
Differential growth factor adsorption to calvarial osteoblast-secreted extracellular matrices instructs osteoblastic behavior.差异生长因子对颅骨成骨细胞分泌的细胞外基质的吸附作用指导成骨细胞的行为。
PLoS One. 2011;6(10):e25990. doi: 10.1371/journal.pone.0025990. Epub 2011 Oct 5.
9
Confocal laser scanning microscopic analysis of collagen scaffolding patterns in cranial sutures.颅骨缝中胶原支架模式的共聚焦激光扫描显微镜分析
J Craniofac Surg. 2008 Jan;19(1):198-203. doi: 10.1097/scs.0b013e31815c8a9a.
10
Surgical correction of metopic synostosis.额缝早闭的手术矫正
Childs Nerv Syst. 2005 May;21(5):392-8. doi: 10.1007/s00381-004-1108-y. Epub 2005 Feb 16.