Granese B - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Page 1

Absence of microcephalin gene mutations in a large cohort of non-consanguineous patients with autosomal recessive primary microcephaly.

Scala I, Titomanlio L, Del Giudice E, Passemard S, Figliuolo C, Annunziata P, Granese B, Scarpato E, Verloes A, Andria G. Scala I, et al. Among authors: granese b. Am J Med Genet A. 2010 Nov;152A(11):2882-5. doi: 10.1002/ajmg.a.33672. Am J Med Genet A. 2010. PMID: 20949544 No abstract available.

Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring.

Scala I, Granese B, Sellitto M, Salomè S, Sammartino A, Pepe A, Mastroiacovo P, Sebastio G, Andria G. Scala I, et al. Among authors: granese b. Genet Med. 2006 Jul;8(7):409-16. doi: 10.1097/01.gim.0000228206.21793.82. Genet Med. 2006. PMID: 16845273 Free article.

Validation of microarray data in human lymphoblasts shows a role of the ubiquitin-proteasome system and NF-kB in the pathogenesis of Down syndrome.

Granese B, Scala I, Spatuzza C, Valentino A, Coletta M, Vacca RA, De Luca P, Andria G. Granese B, et al. BMC Med Genomics. 2013 Jul 5;6:24. doi: 10.1186/1755-8794-6-24. BMC Med Genomics. 2013. PMID: 23830204 Free PMC article.

Re: folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women.

Scala I, Granese B, Lisi A, Mastroiacovo P, Andria G. Scala I, et al. Among authors: granese b. Am J Med Genet A. 2007 May 1;143A(9):1015-7; discussion 1018-9. doi: 10.1002/ajmg.a.31693. Am J Med Genet A. 2007. PMID: 17431899 No abstract available.

Epigallocatechin-3-gallate prevents oxidative phosphorylation deficit and promotes mitochondrial biogenesis in human cells from subjects with Down's syndrome.

Valenti D, De Rasmo D, Signorile A, Rossi L, de Bari L, Scala I, Granese B, Papa S, Vacca RA. Valenti D, et al. Among authors: granese b. Biochim Biophys Acta. 2013 Apr;1832(4):542-52. doi: 10.1016/j.bbadis.2012.12.011. Epub 2013 Jan 2. Biochim Biophys Acta. 2013. PMID: 23291000 Free article.

Activation of the c-Jun N-terminal kinase pathway aggravates proteotoxicity of hepatic mutant Z alpha1-antitrypsin.

Pastore N, Attanasio S, Granese B, Castello R, Teckman J, Wilson AA, Ballabio A, Brunetti-Pierri N. Pastore N, et al. Among authors: granese b. Hepatology. 2017 Jun;65(6):1865-1874. doi: 10.1002/hep.29035. Epub 2017 Apr 10. Hepatology. 2017. PMID: 28073160 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

6 results

Search Page

Filters