Forlino A - Search Results

1

Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain.

Valli M, Sangalli A, Rossi A, Mottes M, Forlino A, Tenni R, Pignatti PF, Cetta G. Valli M, et al. Among authors: forlino a. Eur J Biochem. 1993 Feb 1;211(3):415-9. doi: 10.1111/j.1432-1033.1993.tb17565.x. Eur J Biochem. 1993. PMID: 7679635 Free article.

2

Outer Membrane Vesicles (OMVs) as Biomedical Tools and Their Relevance as Immune-Modulating Agents against H. pylori Infections: Current Status and Future Prospects.

Ahmed AAQ, Besio R, Xiao L, Forlino A. Ahmed AAQ, et al. Among authors: forlino a. Int J Mol Sci. 2023 May 10;24(10):8542. doi: 10.3390/ijms24108542. Int J Mol Sci. 2023. PMID: 37239888 Free PMC article. Review.

3

Structure, evolution and expression of zebrafish cartilage oligomeric matrix protein (COMP, TSP5). CRISPR-Cas mutants show a dominant phenotype in myosepta.

Forte-Gomez HF, Gioia R, Tonelli F, Kobbe B, Koch P, Bloch W, Paulsson M, Zaucke F, Forlino A, Wagener R. Forte-Gomez HF, et al. Among authors: forlino a. Front Endocrinol (Lausanne). 2022 Nov 14;13:1000662. doi: 10.3389/fendo.2022.1000662. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36452329 Free PMC article.

4

Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helix.

Forlino A, Zolezzi F, Valli M, Pignatti PF, Cetta G, Brunelli PC, Mottes M. Forlino A, et al. Hum Mol Genet. 1994 Dec;3(12):2201-6. doi: 10.1093/hmg/3.12.2201. Hum Mol Genet. 1994. PMID: 7881420

5

A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta.

Mottes M, Sangalli A, Valli M, Forlino A, Gomez-Lira M, Antoniazzi F, Constantinou-Deltas CD, Cetta G, Pignatti PF. Mottes M, et al. Among authors: forlino a. Hum Genet. 1994 Jun;93(6):681-7. doi: 10.1007/BF00201570. Hum Genet. 1994. PMID: 8005592

6

Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta.

Cetta G, Rossi A, Tenni R, Valli M, Forlino A, Zanaboni G, Dyne K, Burgio GR. Cetta G, et al. Among authors: forlino a. Connect Tissue Res. 1993;29(1):41-9. doi: 10.3109/03008209309061965. Connect Tissue Res. 1993. PMID: 8339545

7

Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfecta.

Mottes M, Gomez Lira MM, Valli M, Scarano G, Lonardo F, Forlino A, Cetta G, Pignatti PF. Mottes M, et al. Among authors: forlino a. Hum Mutat. 1993;2(3):196-204. doi: 10.1002/humu.1380020308. Hum Mutat. 1993. PMID: 8364588

8

Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta.

Valli M, Rossi A, Forlino A, Tenni R, Cetta G. Valli M, et al. Among authors: forlino a. Matrix. 1993 Jul;13(4):275-80. doi: 10.1016/s0934-8832(11)80022-3. Matrix. 1993. PMID: 8412984

9

A 931 + 2T-->C transition in one COL1A2 allele causes exon 16 skipping in PRO alpha 2(I) mRNA and produces moderately severe OI.

Zolezzi F, Forlino A, Mottes M, Valli M, Sensi A, Calzolari E, Pignatti PF, Cetta G. Zolezzi F, et al. Among authors: forlino a. Hum Mutat. 1995;6(3):268-71. doi: 10.1002/humu.1380060315. Hum Mutat. 1995. PMID: 8535451 No abstract available.

10

Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta.

Dyne KM, Valli M, Forlino A, Mottes M, Kresse H, Cetta G. Dyne KM, et al. Among authors: forlino a. Am J Med Genet. 1996 May 3;63(1):161-6. doi: 10.1002/(SICI)1096-8628(19960503)63:1<161::AID-AJMG28>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723103 Review.

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