Cumulative inactivation of Nell-1 in Wnt1 expressing cell lineages results in craniofacial skeletal hypoplasia and postnatal hydrocephalus-Reference-Cited by-同舟云学术

Cumulative inactivation of Nell-1 in Wnt1 expressing cell lineages results in craniofacial skeletal hypoplasia and postnatal hydrocephalus

Published:2019-10-03 Issue:4 Volume:27 Page:1415-1430
ISSN:1350-9047
Container-title:Cell Death & Differentiation
language:en
Short-container-title:Cell Death Differ

Author:

Chen Xiaoyan,Wang Huiming,Yu Mengliu,Kim Jong Kil,Qi Huichuan,Ha Pin,Jiang Wenlu,Chen Eric,Luo Xiangyou,Needle Ryan Brent,Baik Lloyd,Yang Cathryn,Shi Jiejun,Kwak Jin Hee,Ting Kang,Zhang Xinli,Soo Chia

Funder

Natural Science Foundation of Zhejiang Province

National Natural Science Foundation of China

National Aeronautics and Space Administration

U.S. Department of Health & Human Services | NIH | National Institute of Arthritis and Musculoskeletal and Skin Diseases

UCLA/NIH CTSI

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology

Link

http://www.nature.com/articles/s41418-019-0427-1.pdf

Reference70 articles.

1. Matsuhashi S, Noji S, Koyama E, Myokai F, Ohuchi H, Taniguchi S, et al. New gene, nel, encoding a M(r) 93 K protein with EGF-like repeats is strongly expressed in neural tissues of early stage chick embryos. Dev Dyn. 1995;203:212–22.

2. Watanabe TK, Katagiri T, Suzuki M, Shimizu F, Fujiwara T, Kanemoto N, et al. Cloning and characterization of two novel human cDNAs (NELL1 and NELL2) encoding proteins with six EGF-like repeats. Genomics. 1996;38:273–6.

3. Ting K, Vastardis H, Mulliken JB, Soo C, Tieu A, Do H, et al. Human NELL-1 expressed in unilateral coronal synostosis. J Bone Miner Res: Off J Am Soc Bone Miner Res. 1999;14:80–9.

4. Zhang X, Kuroda S, Carpenter D, Nishimura I, Soo C, Moats R, et al. Craniosynostosis in transgenic mice overexpressing Nell-1. J Clin Investig. 2002;110:861–70.

5. Desai J, Shannon ME, Johnson MD, Ruff DW, Hughes LA, Kerley MK, et al. Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects. Hum Mol Genet. 2006;15:1329–41.

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