about
Relative impact of nucleotide and copy number variation on gene expression phenotypesLattices for ab initio protein structure prediction.p53FamTaG: a database resource of human p53, p63 and p73 direct target genes combining in silico prediction and microarray dataUltradeep sequencing of a human ultraconserved region reveals somatic and constitutional genomic instabilityOrigin and evolution of European community-acquired methicillin-resistant Staphylococcus aureus.Deep sequencing of the X chromosome reveals the proliferation history of colorectal adenomas.Identification of new highly selective inhibitors of the human ADP/ATP carriers by molecular docking and in vitro transport assays.Characterization of Citrus-Associated Alternaria Species in Mediterranean AreasMetazoan OXPHOS gene families: evolutionary forces at the level of mitochondrial and nuclear genomes.Genome duplication and gene-family evolution: the case of three OXPHOS gene families.Evolution, structure and function of mitochondrial carriers: a review with new insights.Molecular modeling of antibodies for the treatment of TNFα-related immunological diseases.AGC1/2, the mitochondrial aspartate-glutamate carriers.Tandem repeats modify the structure of human genes hosted in segmental duplications.Single-nucleotide evolution quantifies the importance of each site along the structure of mitochondrial carriers.Prediction of high- and low-affinity quinol-analogue-binding sites in the aa3 and bo3 terminal oxidases from Bacillus subtilis and Escherichia coli1.An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variants.Evolution of ATP synthase subunit c and cytochrome c gene families in selected Metazoan classes.Biochemical characterization of a new mitochondrial transporter of dephosphocoenzyme A in Drosophila melanogaster.Evolution of nuclearly encoded mitochondrial genes in Metazoa.SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency.Distance-dependent hydrophobic-hydrophobic contacts in protein folding simulations.Heterozygous RNF13 Gain-of-Function Variants Are Associated with Congenital Microcephaly, Epileptic Encephalopathy, Blindness, and Failure to ThriveFAD/NADH Dependent Oxidoreductases: From Different Amino Acid Sequences to Similar Protein Shapes for Playing an Ancient FunctionTranslational Theragnostic of Ovarian Cancer: Where do we stand?CRAT missense variants cause abnormal carnitine acetyltransferase function in an early-onset case of Leigh syndromeProtein structure analysis of the interactions between SARS-CoV-2 spike protein and the human ACE2 receptor: from conformational changes to novel neutralizing antibodies
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Anna De Grassi
@ast
Anna De Grassi
@en
Anna De Grassi
@es
Anna De Grassi
@nl
type
label
Anna De Grassi
@ast
Anna De Grassi
@en
Anna De Grassi
@es
Anna De Grassi
@nl
prefLabel
Anna De Grassi
@ast
Anna De Grassi
@en
Anna De Grassi
@es
Anna De Grassi
@nl
P106
P1153
8660460500
P21
P2798
P31
P496
0000-0001-7273-4263