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A comprehensive proteogenomic pipeline for neoantigen discovery to advance personalized cancer immunotherapy

The neoantigen discovery pipeline NeoDisc incorporates mass spectrometry immunopeptidomics data.

Florian Huber
Marion Arnaud
Michal Bassani-Sternberg
ResearchOpen Access11 Oct 2024
Nature Biotechnology

Volume: 43, P: 1360-1372
Epinephrine affects motility, and increases adhesion, biofilm and virulence of Pseudomonas aeruginosa H103

Mélyssa Cambronel
Damien Tortuel
Nathalie Connil
ResearchOpen Access27 Dec 2019
Scientific Reports

Volume: 9, P: 1-8
Author Correction: Identification of clinically relevant T cell receptors for personalized T cell therapy using combinatorial algorithms

Rémy Pétremand
Johanna Chiffelle
Alexandre Harari
Amendments and CorrectionsOpen Access25 Jun 2024
Nature Biotechnology

Volume: 43, P: 445
A National French consensus on gene lists for the diagnosis of myopathies using next-generation sequencing

Martin Krahn
Valérie Biancalana
Mireille Cossée
Research14 Dec 2018
European Journal of Human Genetics

Volume: 27, P: 349-352
Functional Mitochondrial Heterogeneity in Heteroplasmic Cells Carrying the Mitochondrial DNA Mutation Associated with the MELAS Syndrome (Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes)

Annette Bakker
Cyrille Barthélémy
Anne Lombès
Research01 Aug 2000
Pediatric Research

Volume: 48, P: 143-150
Search for Mitochondrial DNA Heteroplasmy in Neonates Born after Intracytoplasmic Sperm Injection and their Parents † 706

Claude Danan
Andre Van Sterteghem
Serge Amselem
Research01 Apr 1998
Pediatric Research

Volume: 43, P: 123
Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor

Elise Chapiro
Delphine Feldmann
Sandrine Marlin
Research03 Dec 2002
European Journal of Human Genetics

Volume: 10, P: 851-856
MITOCHONDRIAL DNA INHERITANCE IN NEONATES BORN AFTER INTRACYTOPLASMIC SPERM INJECTION. 596

Claude Danan
André Van Steirteghem
Serge Amselem
Research01 Apr 1997
Pediatric Research

Volume: 41, P: 102
Phage-inducible chromosomal minimalist islands (PICMIs), a novel family of small marine satellites of virulent phages

Phage satellites are bacterial genetic elements that co-opt phage machinery for their own dissemination. Here, Barcia-Cruz et al. identify a family of satellites, named PICMIs, that are characterized by reduced gene content and are broadly distributed in marine bacteria of the family Vibrionaceae.

Rubén Barcia-Cruz
David Goudenège
Frédérique Le Roux
ResearchOpen Access22 Jan 2024
Nature Communications

Volume: 15, P: 1-13
A compendium of human gene functions derived from evolutionary modelling

Evolutionary modelling and expert review are applied to integrate experimentally supported knowledge accumulated in the Gene Ontology knowledgebase to create a draft human gene ‘functionome’.

Marc Feuermann
Huaiyu Mi
Paul D. Thomas
ResearchOpen Access26 Feb 2025
Nature

Volume: 640, P: 146-154
Identification of clinically relevant T cell receptors for personalized T cell therapy using combinatorial algorithms

Tumor-reactive T cell receptors are predicted based on single-cell RNA sequencing and single-cell T cell receptor sequencing.

Rémy Pétremand
Johanna Chiffelle
Alexandre Harari
ResearchOpen Access07 May 2024
Nature Biotechnology

Volume: 43, P: 323-328
Impaired surface membrane insertion of homo- and heterodimeric human muscle chloride channels carrying amino-terminal myotonia-causing mutations

Katharina Ronstedt
Damien Sternberg
Christoph Fahlke
ResearchOpen Access27 Oct 2015
Scientific Reports

Volume: 5, P: 1-16
New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome

Marion Masingue
Olivia Cattaneo
Stéphanie Bauché
ResearchOpen Access28 Aug 2023
Scientific Reports

Volume: 13, P: 1-10
A204E mutation in Na_v1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs

Yosuke Kokunai
Carine Dalle
Sophie Nicole
ResearchOpen Access12 Nov 2018
Scientific Reports

Volume: 8, P: 1-10
Substitutions of the S4DIV R2 residue (R1451) in Na_V1.4 lead to complex forms of paramyotonia congenita and periodic paralyses

Hugo Poulin
Pascal Gosselin-Badaroudine
Mohamed Chahine
ResearchOpen Access01 Feb 2018
Scientific Reports

Volume: 8, P: 1-13
PermaNet Dual, a new deltamethrin-chlorfenapyr mixture net, shows improved efficacy against pyrethroid-resistant Anopheles gambiae sensu lato in southern Benin

Thomas Syme
Boris N’dombidjé
Corine Ngufor
ResearchOpen Access28 Jul 2023
Scientific Reports

Volume: 13, P: 1-14

Search

A comprehensive proteogenomic pipeline for neoantigen discovery to advance personalized cancer immunotherapy

Epinephrine affects motility, and increases adhesion, biofilm and virulence of Pseudomonas aeruginosa H103

Author Correction: Identification of clinically relevant T cell receptors for personalized T cell therapy using combinatorial algorithms

A National French consensus on gene lists for the diagnosis of myopathies using next-generation sequencing

Functional Mitochondrial Heterogeneity in Heteroplasmic Cells Carrying the Mitochondrial DNA Mutation Associated with the MELAS Syndrome (Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes)

Search for Mitochondrial DNA Heteroplasmy in Neonates Born after Intracytoplasmic Sperm Injection and their Parents † 706

Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor

MITOCHONDRIAL DNA INHERITANCE IN NEONATES BORN AFTER INTRACYTOPLASMIC SPERM INJECTION. 596

Phage-inducible chromosomal minimalist islands (PICMIs), a novel family of small marine satellites of virulent phages

A compendium of human gene functions derived from evolutionary modelling

Identification of clinically relevant T cell receptors for personalized T cell therapy using combinatorial algorithms

Impaired surface membrane insertion of homo- and heterodimeric human muscle chloride channels carrying amino-terminal myotonia-causing mutations

New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome

A204E mutation in Na_v1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs

Substitutions of the S4DIV R2 residue (R1451) in Na_V1.4 lead to complex forms of paramyotonia congenita and periodic paralyses

PermaNet Dual, a new deltamethrin-chlorfenapyr mixture net, shows improved efficacy against pyrethroid-resistant Anopheles gambiae sensu lato in southern Benin

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