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OTX Genes in Adult Tissues.
Terrinoni A, Micheloni G, Moretti V, Caporali S, Bernardini S, Minieri M, Pieri M, Giaroni C, Acquati F, Costantino L, Ferrara F, Valli R, Porta G. Terrinoni A, et al. Among authors: porta g. Int J Mol Sci. 2023 Nov 30;24(23):16962. doi: 10.3390/ijms242316962. Int J Mol Sci. 2023. PMID: 38069286 Free PMC article. Review.
The mammary gland and the homeobox gene Otx1.
Pagani IS, Terrinoni A, Marenghi L, Zucchi I, Chiaravalli AM, Serra V, Rovera F, Sirchia S, Dionigi G, Miozzo M, Frattini A, Ferrari A, Capella C, Pasquali F, Lo Curto F, Albertini A, Melino G, Porta G. Pagani IS, et al. Among authors: porta g. Breast J. 2010 Sep-Oct;16 Suppl 1:S53-6. doi: 10.1111/j.1524-4741.2010.01006.x. Breast J. 2010. PMID: 21050313 Free article.
Nitric oxide regulates homeoprotein OTX1 and OTX2 expression in the rat myenteric plexus after intestinal ischemia-reperfusion injury.
Filpa V, Carpanese E, Marchet S, Pirrone C, Conti A, Rainero A, Moro E, Chiaravalli AM, Zucchi I, Moriondo A, Negrini D, Crema F, Frigo G, Giaroni C, Porta G. Filpa V, et al. Among authors: porta g. Am J Physiol Gastrointest Liver Physiol. 2017 Apr 1;312(4):G374-G389. doi: 10.1152/ajpgi.00386.2016. Epub 2017 Feb 2. Am J Physiol Gastrointest Liver Physiol. 2017. PMID: 28154013 Free article.
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML.
Rainero A, Angaroni F, D'Avila F, Conti A, Pirrone C, Micheloni G, Tararà L, Millefanti G, Maserati E, Valli R, Spinelli O, Buklijas K, Michelato A, Casalone R, Barlassina C, Barcella M, Sirchia S, Piscitelli E, Caccia M, Porta G. Rainero A, et al. Among authors: porta g. Cell Death Dis. 2018 Mar 2;9(3):349. doi: 10.1038/s41419-018-0387-2. Cell Death Dis. 2018. PMID: 29500381 Free PMC article.
Role of the TAp63 Isoform in Recurrent Nasal Polyps.
Terrinoni A, Palombo R, Pitolli C, Caporali S, De Berardinis R, Ciccarone S, Lanzillotta A, Mauramati S, Porta G, Minieri M, Melino G, Bernardini S, Bruno E. Terrinoni A, et al. Among authors: porta g. Folia Biol (Praha). 2019;65(4):170-180. Folia Biol (Praha). 2019. PMID: 31903890 Free article.
Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype.
Khan AW, Minelli A, Frattini A, Montalbano G, Bogni A, Fabbri M, Porta G, Acquati F, Pinto RM, Bergami E, Mura R, Pegoraro A, Cesaro S, Cipolli M, Zecca M, Danesino C, Locatelli F, Maserati E, Pasquali F, Valli R. Khan AW, et al. Among authors: porta g. Mol Cytogenet. 2020 Jan 2;13:1. doi: 10.1186/s13039-019-0466-9. eCollection 2020. Mol Cytogenet. 2020. PMID: 31908654 Free PMC article.
629 results