Morello R - Search Results

1

CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.

Morello R, Bertin TK, Chen Y, Hicks J, Tonachini L, Monticone M, Castagnola P, Rauch F, Glorieux FH, Vranka J, Bächinger HP, Pace JM, Schwarze U, Byers PH, Weis M, Fernandes RJ, Eyre DR, Yao Z, Boyce BF, Lee B. Morello R, et al. Cell. 2006 Oct 20;127(2):291-304. doi: 10.1016/j.cell.2006.08.039. Cell. 2006. PMID: 17055431 Free article.

2

Cartilage associated protein (CASP) is a novel developmentally regulated chick embryo protein.

Castagnola P, Gennari M, Morello R, Tonachini L, Marin O, Gaggero A, Cancedda R. Castagnola P, et al. Among authors: morello r. J Cell Sci. 1997 Jun;110 ( Pt 12):1351-9. doi: 10.1242/jcs.110.12.1351. J Cell Sci. 1997. PMID: 9217321

3

cDNA cloning, characterization and chromosome mapping of Crtap encoding the mouse cartilage associated protein.

Morello R, Tonachini L, Monticone M, Viggiano L, Rocchi M, Cancedda R, Castagnola P. Morello R, et al. Matrix Biol. 1999 Jun;18(3):319-24. doi: 10.1016/s0945-053x(99)00002-5. Matrix Biol. 1999. PMID: 10429950

4

cDNA cloning, characterization and chromosome mapping of the gene encoding human cartilage associated protein (CRTAP).

Tonachini L, Morello R, Monticone M, Skaug J, Scherer SW, Cancedda R, Castagnola P. Tonachini L, et al. Among authors: morello r. Cytogenet Cell Genet. 1999;87(3-4):191-4. doi: 10.1159/000015463. Cytogenet Cell Genet. 1999. PMID: 10702664

5

Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome.

Morello R, Zhou G, Dreyer SD, Harvey SJ, Ninomiya Y, Thorner PS, Miner JH, Cole W, Winterpacht A, Zabel B, Oberg KC, Lee B. Morello R, et al. Nat Genet. 2001 Feb;27(2):205-8. doi: 10.1038/84853. Nat Genet. 2001. PMID: 11175791

6

Insight into podocyte differentiation from the study of human genetic disease: nail-patella syndrome and transcriptional regulation in podocytes.

Morello R, Lee B. Morello R, et al. Pediatr Res. 2002 May;51(5):551-8. doi: 10.1203/00006450-200205000-00002. Pediatr Res. 2002. PMID: 11978876 Review.

7

Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo.

Zheng Q, Zhou G, Morello R, Chen Y, Garcia-Rojas X, Lee B. Zheng Q, et al. Among authors: morello r. J Cell Biol. 2003 Sep 1;162(5):833-42. doi: 10.1083/jcb.200211089. J Cell Biol. 2003. PMID: 12952936 Free PMC article.

8

Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.

Barnes AM, Chang W, Morello R, Cabral WA, Weis M, Eyre DR, Leikin S, Makareeva E, Kuznetsova N, Uveges TE, Ashok A, Flor AW, Mulvihill JJ, Wilson PL, Sundaram UT, Lee B, Marini JC. Barnes AM, et al. Among authors: morello r. N Engl J Med. 2006 Dec 28;355(26):2757-64. doi: 10.1056/NEJMoa063804. N Engl J Med. 2006. PMID: 17192541 Free PMC article.

9

Uncoupling of chondrocyte differentiation and perichondrial mineralization underlies the skeletal dysplasia in tricho-rhino-phalangeal syndrome.

Napierala D, Sam K, Morello R, Zheng Q, Munivez E, Shivdasani RA, Lee B. Napierala D, et al. Among authors: morello r. Hum Mol Genet. 2008 Jul 15;17(14):2244-54. doi: 10.1093/hmg/ddn125. Epub 2008 Apr 17. Hum Mol Genet. 2008. PMID: 18424451 Free PMC article.

10

Brachy-syndactyly caused by loss of Sfrp2 function.

Morello R, Bertin TK, Schlaubitz S, Shaw CA, Kakuru S, Munivez E, Hermanns P, Chen Y, Zabel B, Lee B. Morello R, et al. J Cell Physiol. 2008 Oct;217(1):127-37. doi: 10.1002/jcp.21483. J Cell Physiol. 2008. PMID: 18446812 Free PMC article.

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