Bisello G - Search Results

1

New variants of AADC deficiency expand the knowledge of enzymatic phenotypes.

Montioli R, Bisello G, Dindo M, Rossignoli G, Voltattorni CB, Bertoldi M. Montioli R, et al. Among authors: bisello g. Arch Biochem Biophys. 2020 Mar 30;682:108263. doi: 10.1016/j.abb.2020.108263. Epub 2020 Jan 15. Arch Biochem Biophys. 2020. PMID: 31953134

2

Cysteine 180 Is a Redox Sensor Modulating the Activity of Human Pyridoxal 5'-Phosphate Histidine Decarboxylase.

Rossignoli G, Grottesi A, Bisello G, Montioli R, Borri Voltattorni C, Paiardini A, Bertoldi M. Rossignoli G, et al. Among authors: bisello g. Biochemistry. 2018 Nov 6;57(44):6336-6348. doi: 10.1021/acs.biochem.8b00625. Epub 2018 Oct 29. Biochemistry. 2018. PMID: 30346159

3

Oxygen reactivity with pyridoxal 5'-phosphate enzymes: biochemical implications and functional relevance.

Bisello G, Longo C, Rossignoli G, Phillips RS, Bertoldi M. Bisello G, et al. Amino Acids. 2020 Aug;52(8):1089-1105. doi: 10.1007/s00726-020-02885-6. Epub 2020 Aug 25. Amino Acids. 2020. PMID: 32844248 Free PMC article. Review.

4

Tyrosine Phosphorylation Modulates Peroxiredoxin-2 Activity in Normal and Diseased Red Cells.

Mattè A, Federti E, Tibaldi E, Di Paolo ML, Bisello G, Bertoldi M, Carpentieri A, Pucci P, Iatchencko I, Wilson AB, Riccardi V, Siciliano A, Turrini F, Kim DW, Choi SY, Brunati AM, De Franceschi L. Mattè A, et al. Among authors: bisello g. Antioxidants (Basel). 2021 Feb 1;10(2):206. doi: 10.3390/antiox10020206. Antioxidants (Basel). 2021. PMID: 33535382 Free PMC article.

5

Aromatic l-amino acid decarboxylase deficiency: a patient-derived neuronal model for precision therapies.

Rossignoli G, Krämer K, Lugarà E, Alrashidi H, Pope S, De La Fuente Barrigon C, Barwick K, Bisello G, Ng J, Counsell J, Lignani G, Heales SJR, Bertoldi M, Barral S, Kurian MA. Rossignoli G, et al. Among authors: bisello g. Brain. 2021 Sep 4;144(8):2443-2456. doi: 10.1093/brain/awab123. Brain. 2021. PMID: 33734312 Free PMC article.

6

Compound heterozygosis in AADC deficiency: A complex phenotype dissected through comparison among heterodimeric and homodimeric AADC proteins.

Longo C, Montioli R, Bisello G, Palazzi L, Mastrangelo M, Brennenstuhl H, de Laureto PP, Opladen T, Leuzzi V, Bertoldi M. Longo C, et al. Among authors: bisello g. Mol Genet Metab. 2021 Sep-Oct;134(1-2):147-155. doi: 10.1016/j.ymgme.2021.08.011. Epub 2021 Aug 28. Mol Genet Metab. 2021. PMID: 34479793

7

The novel P330L pathogenic variant of aromatic amino acid decarboxylase maps on the catalytic flexible loop underlying its crucial role.

Bisello G, Kusmierska K, Verbeek MM, Sykut-Cegielska J, Willemsen MAAP, Wevers RA, Szymańska K, Poznanski J, Drozak J, Wertheim-Tysarowska K, Rygiel AM, Bertoldi M. Bisello G, et al. Cell Mol Life Sci. 2022 May 20;79(6):305. doi: 10.1007/s00018-022-04343-w. Cell Mol Life Sci. 2022. PMID: 35593933 Free PMC article.

8

Compound Heterozygosis in AADC Deficiency and Its Complex Phenotype in Terms of AADC Protein Population.

Bisello G, Bertoldi M. Bisello G, et al. Int J Mol Sci. 2022 Sep 23;23(19):11238. doi: 10.3390/ijms231911238. Int J Mol Sci. 2022. PMID: 36232540 Free PMC article. Review.

9

Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.

Himmelreich N, Bertoldi M, Alfadhel M, Alghamdi MA, Anikster Y, Bao X, Bashiri FA, Zeev BB, Bisello G, Ceylan AC, Chien YH, Choy YS, Elsea SH, Flint L, García-Cazorla À, Gijavanekar C, Gümüş EY, Hamad MH, Hişmi B, Honzik T, Hübschmann OK, Hwu WL, Ibáñez-Micó S, Jeltsch K, Juliá-Palacios N, Kasapkara ÇS, Kurian MA, Kusmierska K, Liu N, Ngu LH, Odom JD, Ong WP, Opladen T, Oppeboen M, Pearl PL, Pérez B, Pons R, Rygiel AM, Shien TE, Spaull R, Sykut-Cegielska J, Tabarki B, Tangeraas T, Thöny B, Wassenberg T, Wen Y, Yakob Y, Yin JGC, Zeman J, Blau N. Himmelreich N, et al. Among authors: bisello g. Mol Genet Metab. 2023 Jul;139(3):107624. doi: 10.1016/j.ymgme.2023.107624. Epub 2023 Jun 2. Mol Genet Metab. 2023. PMID: 37348148 Free article.

10

Exome sequencing data screening to identify undiagnosed Aromatic l-amino acid decarboxylase deficiency in neurodevelopmental disorders.

Riva A, Iacomino M, Piccardo C, Franceschetti L, Franchini R, Baroni A, Minetti C, Bisello G, Zara F, Scala M, Striano P, Bertoldi M. Riva A, et al. Among authors: bisello g. Biochem Biophys Res Commun. 2023 Sep 17;673:131-136. doi: 10.1016/j.bbrc.2023.06.065. Epub 2023 Jun 19. Biochem Biophys Res Commun. 2023. PMID: 37385007

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

18 results

Search Page

Filters