Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome-Reference-Cited by-同舟云学术

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Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

Published:1998-05 Issue:1 Volume:19 Page:47-50
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Dreyer Sandra D.,Zhou Guang,Baldini Antonio,Winterpacht Andreas,Zabel Bernhard,Cole William,Johnson Randy L.,Lee Brendan

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0598-47.pdf

Reference22 articles.

1. Johnson, R.L. & Tabin, C.J. Molecular models for vertebrate limb development. Cell 90, 979–990 (1997).

2. Chen, H et al. Limb and kidney defects in Lmxlb mutant mice suggest an involvement of LMX1B in human nail patella syndrome. Nature Genet. 19, 51–55 (1998).

3. Schmeichel, K.L. & Beckerle, M.C. Molecular dissection of a LIM domain. Mol. Biol. Cell 8, 219–230 (1997).

4. Feuerstein, R., Wang, X., Song, D., Cooke, N.E. & Liebhaber, S.A., LIM/double zinc-finger motif functions as a protein dimerization domain. Proc. Natl. Acad. Sci. USA 91, 10655–10659 (1994).

5. Schmeichel, K.L. & Beckerle, M.C. The LIM domain is a modular protein-binding interface. Cell 79, 211–219 (1994).

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