Search Results - "Coatti, Giuliana C"

Genistein Affects Expression of Cytochrome P450 (CYP450) Genes in Hepatocellular Carcinoma (HEPG2/C3A) Cell Line by Lepri, Sandra R, Sartori, Daniele, Semprebon, Simone C, Baranoski, Adrivanio, Coatti, Giuliana C, Mantovani, Mario S

“…Genistein (5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one) is the most abundant isoflavone in soybean, which has been associated with a lower risk of…”
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Dual SMAD inhibition enhances the longevity of human epididymis epithelial cells by Coatti, Giuliana C., Paranjapye, Alekh, Harris, Ann

“…Primary human epididymis epithelial (HEE) cells are valuable reagents for functional studies on the human epididymis. We used them previously to determine the…”
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A promoter-dependent upstream activator augments CFTR expression in diverse epithelial cell types by Coatti, Giuliana C., Vaghela, Nirbhayaditya, Gillurkar, Pulak, Leir, Shih-Hsing, Harris, Ann

“…The cystic fibrosis transmembrane conductance regulator (CFTR) gene encodes an anion-selective channel found in epithelial cell membranes. Mutations in CFTR…”
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The impact of genomic distance on enhancer‐promoter interactions at the CFTR locus by Kerschner, Jenny L., Meckler, Frederick, Coatti, Giuliana C., Vaghela, Nirbhayaditya, Paranjapye, Alekh, Harris, Ann

“…We identified and characterized multiple cell‐type selective enhancers of the CFTR gene promoter in previous work and demonstrated active looping of these…”
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An epilepsy‐associated ACTL6B variant captures neuronal hyperexcitability in a human induced pluripotent stem cell model by Ahn, Lucie Y., Coatti, Giuliana C., Liu, Jingyi, Gumus, Evren, Schaffer, Ashleigh E., Miranda, Helen C.

“…ACTL6B is a component of the neuronal BRG1/brm‐associated factor (nBAF) complex, which is required for chromatin remodeling in postmitotic neurons. We recently…”
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Random changepoint segmented regression with smooth transition by Singer, Julio M, Rocha, Francisco MM, Pedroso-de-Lima, Antonio Carlos, Silva, Giovani L, Coatti, Giuliana C, Zatz, Mayana

“…We consider random changepoint segmented regression models to analyse data from a study conducted to verify whether treatment with stem cells may delay the…”
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Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome by Melo, Uirá S, Macedo-Souza, Lucia I, Figueiredo, Thalita, Muotri, Alysson R, Gleeson, Joseph G, Coux, Gabriela, Armas, Pablo, Calcaterra, Nora B, Kitajima, João P, Amorim, Simone, Olávio, Thiago R, Griesi-Oliveira, Karina, Coatti, Giuliana C, Rocha, Clarissa R R, Martins-Pinheiro, Marinalva, Menck, Carlos F M, Zaki, Maha S, Kok, Fernando, Zatz, Mayana, Santos, Silvana

“…SPOAN syndrome is a neurodegenerative disorder mainly characterized by spastic paraplegia, optic atrophy and neuropathy (SPOAN). Affected patients are…”
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