Matteo P. Ferla

发表

New rRNA Gene-Based Phylogenies of the Alphaproteobacteria Provide Perspective on Major Groups, Mitochondrial Ancestry and Phylogenetic Instability

S. Giovannoni, Matteo P. Ferla, J. C. Thrash, 2013, PloS one.

Open Science Discovery of Potent Non-Covalent SARS-CoV-2 Main Protease Inhibitors

Vincent A. Voelz, Matthew F. D. Hurley, R. Glen, 2020, bioRxiv.

Fragment binding to the Nsp3 macrodomain of SARS-CoV-2 identified through crystallographic screening and computational docking

A. Ashworth, J. Irwin, B. Shoichet, 2020, Science Advances.

Eumalacostracan phylogeny and total evidence: limitations of the usual suspects

R. Jenner, Matteo P. Ferla, M. Wills, 2009, BMC Evolutionary Biology.

Identification of Circulating Genomic and Metabolic Biomarkers in Intrahepatic Cholangiocarcinoma

S. Knight, Matteo P. Ferla, Jenny C. Taylor, 2019, Cancers.

Non-coding variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms

M. Hurles, K. Karczewski, P. Danecek, 2020, medRxiv.

A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.

Anthony R. Dallosso, J. Rosenfeld, A. Pagnamenta, 2021, American journal of human genetics.

Structure-based inhibitor optimization for the Nsp3 Macrodomain of SARS-CoV-2

Yurii S. Moroz, J. Irwin, B. Shoichet, 2022, bioRxiv.

Pervasive cooperative mutational effects on multiple catalytic enzyme traits emerge via long-range conformational dynamics

Matteo P. Ferla, M. Reetz, Sílvia Osuna, 2020, Nature Communications.

Primordial‐like enzymes from bacteria with reduced genomes

G. Evans, Matteo P. Ferla, W. Patrick, 2017, Molecular microbiology.

Variable skeletal phenotypes associated with biallelic variants in PRKG2

A. Pagnamenta, Matteo P. Ferla, Jenny C. Taylor, 2021, Journal of Medical Genetics.

Iterative computational design and crystallographic screening identifies potent inhibitors targeting the Nsp3 Macrodomain of SARS-CoV-2

Yurii S. Moroz, J. Irwin, B. Shoichet, 2022, bioRxiv.

Evolving Accelerated Amidation by SpyTag/SpyCatcher to Analyze Membrane Dynamics

Matteo P. Ferla, Anusuya Banerjee, M. Howarth, 2017, Angewandte Chemie.

Directed Evolution of Proteins Based on Mutational Scanning.

Manfred T Reetz, Carlos G Acevedo-Rocha, Matteo Ferla, 2018, Methods in molecular biology.

Bacterial methionine biosynthesis.

Matteo P. Ferla, W. Patrick, M. Ferla, 2014, Microbiology.

DogCatcher allows loop-friendly protein-protein ligation

Matteo P. Ferla, M. Howarth, R. Bon, 2021, Cell chemical biology.

Biallelic PI4KA variants cause neurological, intestinal and immunological disease

P. De Camilli, H. Cross, Matteo P. Ferla, 2021, Brain : a journal of neurology.

SARS-CoV-2 infects the human kidney and drives fibrosis in kidney organoids

Ivan G. Costa, Vincent A. Voelz, Matthew F. D. Hurley, 2021, Cell Stem Cell.

Fragment binding to the Nsp3 macrodomain of SARS-CoV-2 identified through crystallographic screening and computational docking

A. Ashworth, J. Irwin, B. Shoichet, 2021, Science Advances.

Iterative computational design and crystallographic screening identifies potent inhibitors targeting the Nsp3 macrodomain of SARS-CoV-2

Yurii S. Moroz, J. Irwin, B. Shoichet, 2023, Proceedings of the National Academy of Sciences of the United States of America.

Venus: Elucidating the Impact of Amino Acid Variants on Protein Function Beyond Structure Destabilisation

A. Pagnamenta, Matteo P. Ferla, Jenny C. Taylor, 2022, Journal of molecular biology.

Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities

A. V. Vulto-van Silfhout, D. Baralle, P. Striano, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Clinico‐radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiency

P. Striano, H. Prokisch, Matteo P. Ferla, 2022, Human mutation.

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy

Katherine R. Smith, M. B. Pereira, A. Need, 2021, Brain : a journal of neurology.

Biallelic variants in SLC38A3 encoding a glutamine transporter cause epileptic encephalopathy.

J. Rosenfeld, J. Lupski, R. Gibbs, 2021, Brain : a journal of neurology.

MichelaNglo: sculpting protein views on web pages without coding

Jenny C Taylor, Brian D Marsden, David Damerell, 2020, Bioinform..

Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome

A. Pagnamenta, Matteo P. Ferla, Jenny C. Taylor, 2019, Clinical genetics.

Expanding the phenotypic spectrum of BCS1L‐related mitochondrial disease

V. Fellman, Matteo P. Ferla, Jenny C. Taylor, 2021, Annals of clinical and translational neurology.

Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders

J. Lupski, S. Lalani, Matteo P. Ferla, 2023, Brain : a journal of neurology.

Bacterial methionine biosynthesis.

Matteo P. Ferla, W. Patrick, 2014, Microbiology.

The origin and ecological significance of multiple branches for histidine utilization in Pseudomonas aeruginosa PAO1.

Monica L Gerth, Paul B Rainey, Matteo P Ferla, 2012, Environmental microbiology.

Mutanalyst, an online tool for assessing the mutational spectrum of epPCR libraries with poor sampling

Matteo Paolo Ferla, Matteo P. Ferla, 2016, BMC Bioinformatics.

SARS-CoV-2 infects the human kidney and drives fibrosis in kidney organoids

Ivan G. Costa, Vincent A. Voelz, Matthew F. D. Hurley, 2021, Cell Stem Cell.