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  • 1-10 ل  64 نتائج ل ""MESH: Phenotype""

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Collection : Institut Pasteur
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Academic Journal

MANOCCA: a robust and computationally efficient test of covariance in high-dimension multivariate omics data

Subjects: biomarkers; correlation; covariance

  • Source: ISSN: 1467-5463.

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Academic Journal

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development

Subjects: XY DSD; Cytogenetic abnormalities; Disorders of sex development (DSD)46

  • Source: ISSN: 1477-7827 ; Reproductive Biology and Endocrinology ; https://hal.science/hal-04150358 ; Reproductive Biology and Endocrinology, 2023, 21 (1), pp.2. ⟨10.1186/s12958-022-01045-7⟩.

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Academic Journal

Plasticity of Dopaminergic Phenotype and Locomotion in Larval Zebrafish Induced by Brain Excitability Changes during the Embryonic Period

Subjects: differentiation; dopamine; locomotion

  • Source: ISSN: 2373-2822 ; eNeuro ; https://hal.science/hal-04178115 ; eNeuro, 2023, 10 (6), pp.0320-21. ⟨10.1523/ENEURO.0320-21.2023⟩.

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Academic Journal

The tumor suppressor adenomatous polyposis coli regulates T lymphocyte migration

Subjects: MESH: Adenomatous Polyposis Coli; MESH: Adenomatous Polyposis Coli Protein; MESH: Cell Movement

  • Source: ISSN: 2375-2548 ; Science Advances ; https://pasteur.hal.science/pasteur-03681845 ; Science Advances , 2022, 8 (15), pp.eabl5942. ⟨10.1126/sciadv.abl5942⟩.

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Academic Journal

Phenotypic and genomic hallmarks of a novel, potentially pathogenic rapidly growing Mycobacterium species related to the Mycobacterium fortuitum complex

Subjects: MESH: Computational Biology; MESH: Gene Transfer; Horizontal

  • Source: ISSN: 2045-2322.

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Academic Journal

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

Subjects: MESH: Audiometry; MESH: Base Sequence; MESH: Carrier Proteins

  • Source: ISSN: 1932-6203.

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Academic Journal

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy

Subjects: CCDC51; MITOK; candidate gene

  • Source: ISSN: 1661-6596.

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Academic Journal

Multitrait GWAS to connect disease variants and biological mechanisms

Subjects: MESH: Cluster Analysis; MESH: Computational Biology; MESH: Genetic Predisposition to Disease

  • Source: ISSN: 1553-7390.

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Academic Journal

Dichotomous metabolic networks govern human ILC2 proliferation and function

Subjects: MESH: Amino Acids; Branched-Chain; MESH: Arginine

  • Source: ISSN: 1529-2908.

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Academic Journal

Editorial: Infectious Agent-Induced Chronic Immune Activation: Causes, Phenotypes, and Consequences

Subjects: Comorbidity; Immune cell; Immune system

  • Source: ISSN: 1664-3224.

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  • 1-10 ل  64 نتائج ل ""MESH: Phenotype""