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Hypercalcémie aggravée par l’administration de vitamine D chez un patient adulte révélant une mutation hétérozygote composite CYP24A1 : réponse et traitement à long terme par rifampicine.

• Authors : Parotte, Marie Christine; VALDES SOCIN, Hernan Gonzalo; CAVALIER, Etienne

Subjects: hypercalcemia; vitamin D; CYP24A1

• Source: Annales d'Endocrinologie, 82, 311 (2021-10-01); Societe Francaise d'Endocrinologie, Le Havre, France [FR], 13-16 octobre 2021

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How Closely are Common Mutation Operators Coupled to Real Faults?

• Authors : Gay, Gregory, 1987; Salahirad, Alireza

Subjects: Programvaruteknik; Software Engineering; Fault Analysis

• Source: 2023 IEEE Conference on Software Testing, Verification and Validation (ICST).

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Mutation Testing in Continuous Integration: An Exploratory Industrial Case Study

• Authors : Örgård, Jonathan; Gay, Gregory, 1987; Gomes, Francisco, 1987

Subjects: Programvaruteknik; Software Engineering; C++

• Source: 2023 IEEE International Conference on Software Testing, Verification and Validation Workshops (ICSTW).

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Congenital hyperinsulinism due to a new mutation in the gene ABCC8

• Authors : Katschen, Sophie; Arnoux, Jean-Baptiste; de HALLEUX, Virginie

Subjects: Human health sciences; Pediatrics; Endocrinology, metabolism & nutrition

• Source: Climate changes in pediatrics: from society to environment, Bruxelles, Belgium [BE], Du 16 au 17 mars 2023

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A hypomorphic mutation in the ATP2A1 gene increases muscle mass yet compromises meat quality of Belgian Blue cattle

• Authors : Rombouts, T; Druet, Tom; Gualdron Duarte, Jose Luis

Subjects: Life sciences; Animal production & animal husbandry; Veterinary medicine & animal health

• Source: World Congress on Genetics Applied to Livestock Production, Rotterdam, Netherlands [NL], 3-8 Juillet 2022

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It’s all in their eyes: a three-generation family with branchio-oculo-facial syndrome (BOFS) reveals a heterozygous novel mutation in TFAP2A gene.

• Authors : VALDES SOCIN, Hernan Gonzalo; ANDRIS, Cécile; CROMMEN, Jessica

Subjects: coloboma; branchio-oculo-facial syndrome; TFAP2A

• Source: Acta Clinica Belgica, 2 (76), 27-29 (2021-12); Annual Congress of the Belgian Society of Internal Medicine, Bruxelles, Belgium [BE], 10-11 december 2021

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Une rare mutation du gène KIF5A associée à un tableau de CMT2 sans signe de spasticité : cas clinique

• Authors : Dellatte, Julien; LIEVENS, Isabelle; WANG, François-Charles

Subjects: Human health sciences; Neurology; Sciences de la santé humaine

• Source: 22èmes Journées Francophones d'ElectroNeuroMyoGraphie, Marrakech, Morocco [MA], 18-20 mai 2022

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Chaotic mutation strategy based single candidate optimizer algorithm

• Authors : Emek, Halil İbrahim; Yüzgeç, Uğur;

Subjects: Heuristic; Mutation; Chaotic

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FairPipes: Data Mutation Pipelines for Machine Learning Fairness

• Authors : Molinier, Camille; Temple, Paul; Perrouin, Gilles ...

Subjects: Machine Learning; Fairness; Mutation TestingLisbonne; Portugal

• Source: AST 2024 - 5th ACM/IEEE International Conference on Automation of Software Test ; https://hal.science/hal-04440201 ; AST 2024 - 5th ACM/IEEE International Conference on Automation of Software Test,

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Assessing Reflection Usage with Mutation Testing Augmented Analysis

• Authors : Thomas, Iona; Ducasse, Stéphane; Polito, Guillermo ...

Subjects: Reflection; Mutation Analysis; Smalltalk-PharoLimassol; Cyprus

• Source: 21st International Conference on Software and Systems Reuse (ICSR 2024)https://inria.hal.science/hal-0460010121st International Conference on Software and Systems Reuse (ICSR 2024), Jun

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