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  • 1-10 ل  370 نتائج ل ""Mutation""

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Collection : Ephe (Ecole Pratique Des Hautes Etudes, Paris)
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Dissertation/ Thesis

Role of NADPH oxidase 4 (NOX4) in the dedifferentiation of thyroid tumor cells harboring BRAFV600E mutation ; Rôle de la NADPH oxydase 4 (NOX4) dans la dédifférenciation des cellules tumorales thyroïdiennes porteuses de la mutation BRAFV600E

Subjects: Papillary thyroid cancer; BRAFV600E mutation; NADPH oxidase 4 (NOX4)

  • Source: https://theses.hal.science/tel-04552540 ; Cancer. Université Paris-Saclay, 2024. Français. ⟨NNT : 2024UPASL012⟩.

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Academic Journal

The Most Common VHL Point Mutation R167Q in Hereditary VHL Disease Interferes with Cell Plasticity Regulation

Subjects: ccRCCs; R167Q VHL mutation; hypoxia-related genes

  • Source: ISSN: 2072-6694.

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Academic Journal

The Most Common VHL Point Mutation R167Q in Hereditary VHL Disease Interferes with Cell Plasticity Regulation

Subjects: ccRCCs; R167Q VHL mutation; hypoxia-related genes

  • Source: ISSN: 2072-6694.

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Academic Journal

Analyses of displacements resulting from a point mutation in proteins

Subjects: point mutation; protein structure; allosteric effect

  • Source: ISSN: 1047-8477.

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Academic Journal

Outcomes of Patients With Advanced NSCLC From the Intergroupe Francophone de Cancérologie Thoracique Biomarkers France Study by KRAS Mutation Subtypes

Subjects: KRAS mutation; Non-small cell lung cancer; NSCLC

  • Source: ISSN: 2666-3643.

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Academic Journal

The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiency

Subjects: C9orf72; Frontotemporal dementia; Frontotemporal lobar degeneration

  • Source: ISSN: 0197-4580 ; Neurobiology of Aging ; https://hal.science/hal-03488651 ; Neurobiology of Aging, 2020, 85, pp.154.e9 - 154.e11. ⟨10.1016/j.neurobiolaging.2019.06.002⟩.

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Academic Journal

Genomic mutation landscape of skin cancers from DNA repair-deficient xeroderma pigmentosum patients

Subjects: [SDV]Life Sciences [q-bio]

  • Source: ISSN: 2041-1723.

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Report

Monitoring the propagation of SARS CoV2 variants by tracking identified mutation in wastewater using specific RT-qPCR

Subjects: SARS - CoV-2; COVID-19; variant

  • Source: https://hal.sorbonne-universite.fr/hal-03260967 ; 2021.

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Academic Journal

A frame-shift mutation in COMTD1 is associated with impaired pheomelanin pigmentation in chicken

Subjects: [SDV]Life Sciences [q-bio]

  • Source: ISSN: 1553-7390.

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Academic Journal

Different outcome of sarcoglycan missense mutation between human and mouse

Subjects: MESH: Amino Acid Sequence; MESH: Amino Acid Substitution; MESH: Muscle

  • Source: ISSN: 1932-6203.

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  • 1-10 ل  370 نتائج ل ""Mutation""