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Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders.
Am J Med Genet A. 2017 Jun;173(6):1649-1655. doi: 10.1002/ajmg.a.38205. Epub 2017 Apr 13.
Am J Med Genet A. 2017.
PMID: 28407444
Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response.
Fichera M, Barone R, Grillo L, De Grandi M, Fiore V, Morana I, Maniscalchi T, Vinci M, Amata S, Spalletta A, Sorge G, Signorelli SS.
Fichera M, et al. Among authors: de grandi m.
Mol Cytogenet. 2014 Dec 19;7(1):90. doi: 10.1186/s13039-014-0090-7. eCollection 2014.
Mol Cytogenet. 2014.
PMID: 25540671
Free PMC article.
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4-Hydroxynonenal inhibits telomerase activity and hTERT expression in human leukemic cell lines.
Pizzimenti S, Briatore F, Laurora S, Toaldo C, Maggio M, De Grandi M, Meaglia L, Menegatti E, Giglioni B, Dianzani MU, Barrera G.
Pizzimenti S, et al. Among authors: de grandi m.
Free Radic Biol Med. 2006 May 1;40(9):1578-91. doi: 10.1016/j.freeradbiomed.2005.12.024. Epub 2006 Jan 19.
Free Radic Biol Med. 2006.
PMID: 16632118
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Changes in bone volume and bone resorption by olpadronate treatment in an experimental model of uremic bone disease.
Tomat A, Gamba CA, Mandalunis P, De Grandi MC, Somoza J, Friedman S, Zeni S.
Tomat A, et al. Among authors: de grandi mc.
J Musculoskelet Neuronal Interact. 2005 Jun;5(2):174-81.
J Musculoskelet Neuronal Interact. 2005.
PMID: 15951635
Free article.
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