Syndactyly in a novel Fras1 rdf mutant results from interruption of signals for interdigital apoptosis-Reference-Cited by-同舟云学术

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Syndactyly in a novel Fras1 rdf mutant results from interruption of signals for interdigital apoptosis

Published:2016-02-24 Issue:4 Volume:245 Page:497-507
ISSN:1058-8388
Container-title:Developmental Dynamics
language:en
Short-container-title:Dev. Dyn.

Author:

Hines Elizabeth A.¹,Verheyden Jamie M.¹,Lashua Amber J.¹,Larson Sarah C.¹,Branchfield Kelsey¹,Domyan Eric T.¹,Gao Juan²,Harvey Julie F.¹,Herriges John C.¹,Hu Linghan³,Mcculley David J.¹,Throckmorton Kurt¹,Yokoyama Shigetoshi¹,Ikeda Akihiro¹,Xu Guoliang²,Sun Xin¹

Affiliation:

1. Laboratory of Genetics University of Wisconsin Madison; WI 53706

2. Institute of Biochemistry and Cell Biology Shanghai Institute for Biological Sciences Chinese Academy of Sciences Shanghai; China 200031

3. Zhiyuan College Shanghai Jiao Tong University Shanghai; China 200240

Funder

American Heart

March of Dimes

NHLBI

Publisher

Wiley

Subject

Developmental Biology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/dvdy.24389/fullpdf

Reference43 articles.

1. A high throughput in situ hybridization method to characterize mRNA expression patterns in the fetal mouse lower urogenital tract;Abler;J Vis Exp,2011

2. Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis;Bandyopadhyay;PLoS Genet,2006

3. Fraser syndrome: epidemiological study in a European population;Barisic;Am J Med Genet A,2013

4. The role of integrin alpha8beta1 in fetal lung morphogenesis and injury;Benjamin;Dev Biol,2009

5. SMAD 8 binding to mice Msx1 basal promoter is required for transcriptional activation;Binato;Biochem J,2006

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The Fraser complex interconnects tissue layers to support basal epidermis and osteoblast integrated morphogenesis underlying fin skeletal patterning;2023-07-09

2. “Hypothesis: Patient with possible disturbance in programmed cell death”: further insights in pathogenicity and clinical features of Fraser syndrome;European Journal of Human Genetics;2022-08-30

3. Orpha disease – FRASER syndrome (ORPHA:2052) in children: phenotype and genotype characteristics;Nephrology (Saint-Petersburg);2021-04-23

4. Fraser syndrome: review of the literature illustrated by a historical adult case;International Journal of Oral and Maxillofacial Surgery;2020-10

5. Evo-Devo Path as a Bridge between Evolution, Morphological Disparity, and Medicine with Comments on “Hopeful Monsters” in the Age of Genomics;Current Molecular Biology Reports;2020-05-16

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