Raghunath M - Search Results

1

The Tight skin mouse: demonstration of mutant fibrillin-1 production and assembly into abnormal microfibrils.

Kielty CM, Raghunath M, Siracusa LD, Sherratt MJ, Peters R, Shuttleworth CA, Jimenez SA. Kielty CM, et al. Among authors: raghunath m. J Cell Biol. 1998 Mar 9;140(5):1159-66. doi: 10.1083/jcb.140.5.1159. J Cell Biol. 1998. PMID: 9490728 Free PMC article.

2

Truncated profibrillin of a Marfan patient is of apparent similar size as fibrillin: intracellular retention leads to over-N-glycosylation.

Raghunath M, Kielty CM, Steinmann B. Raghunath M, et al. J Mol Biol. 1995 May 19;248(5):901-9. doi: 10.1006/jmbi.1995.0270. J Mol Biol. 1995. PMID: 7760331

3

Analyses of truncated fibrillin caused by a 366 bp deletion in the FBN1 gene resulting in Marfan syndrome.

Raghunath M, Kielty CM, Kainulainen K, Child A, Peltonen L, Steinmann B. Raghunath M, et al. Biochem J. 1994 Sep 15;302 ( Pt 3)(Pt 3):889-96. doi: 10.1042/bj3020889. Biochem J. 1994. PMID: 7945217 Free PMC article.

4

A point mutation creating an extra N-glycosylation site in fibrillin-1 results in neonatal Marfan syndrome.

Lönnqvist L, Karttunen L, Rantamäki T, Kielty C, Raghunath M, Peltonen L. Lönnqvist L, et al. Among authors: raghunath m. Genomics. 1996 Sep 15;36(3):468-75. doi: 10.1006/geno.1996.0492. Genomics. 1996. PMID: 8884270

5

Carboxy-terminal conversion of profibrillin to fibrillin at a basic site by PACE/furin-like activity required for incorporation in the matrix.

Raghunath M, Putnam EA, Ritty T, Hamstra D, Park ES, Tschödrich-Rotter M, Peters R, Rehemtulla A, Milewicz DM. Raghunath M, et al. J Cell Sci. 1999 Apr;112 ( Pt 7):1093-100. doi: 10.1242/jcs.112.7.1093. J Cell Sci. 1999. PMID: 10198291

6

The cutaneous microfibrillar apparatus contains latent transforming growth factor-beta binding protein-1 (LTBP-1) and is a repository for latent TGF-beta1.

Raghunath M, Unsöld C, Kubitscheck U, Bruckner-Tuderman L, Peters R, Meuli M. Raghunath M, et al. J Invest Dermatol. 1998 Oct;111(4):559-64. doi: 10.1046/j.1523-1747.1998.00339.x. J Invest Dermatol. 1998. PMID: 9764833 Free article.

7

Fibrillin and elastin expression in skin regenerating from cultured keratinocyte autografts: morphogenesis of microfibrils begins at the dermo-epidermal junction and precedes elastic fiber formation.

Raghunath M, Bächi T, Meuli M, Altermatt S, Gobet R, Bruckner-Tuderman L, Steinmann B. Raghunath M, et al. J Invest Dermatol. 1996 May;106(5):1090-5. doi: 10.1111/1523-1747.ep12339373. J Invest Dermatol. 1996. PMID: 8618045 Free article.

8

Abnormal morphology of fibrillin microfibrils in fibroblast cultures from patients with neonatal Marfan syndrome.

Godfrey M, Raghunath M, Cisler J, Bevins CL, DePaepe A, Di Rocco M, Gregoritch J, Imaizumi K, Kaplan P, Kuroki Y, et al. Godfrey M, et al. Among authors: raghunath m. Am J Pathol. 1995 Jun;146(6):1414-21. Am J Pathol. 1995. PMID: 7778680 Free PMC article.

9

Confocal laser scanning analysis of the association of fibulin-2 with fibrillin-1 and fibronectin define different stages of skin regeneration.

Raghunath M, Tschödrich-Rotter M, Sasaki T, Meuli M, Chu ML, Timpl R. Raghunath M, et al. J Invest Dermatol. 1999 Jan;112(1):97-101. doi: 10.1046/j.1523-1747.1999.00483.x. J Invest Dermatol. 1999. PMID: 9886271 Free article.

10

A rare branch-point mutation is associated with missplicing of fibrillin-2 in a large family with congenital contractural arachnodactyly.

Maslen C, Babcock D, Raghunath M, Steinmann B. Maslen C, et al. Among authors: raghunath m. Am J Hum Genet. 1997 Jun;60(6):1389-98. doi: 10.1086/515472. Am J Hum Genet. 1997. PMID: 9199560 Free PMC article.

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