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  • 1-10 ل  61,804 نتائج ل ""Phenotype""

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Publisher : wiley
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Academic Journal

Early Language Impairment as an Integral Part of the Cognitive Phenotype in Huntington's Disease

Subjects: cognitive phenotype; language; neuroimaging

  • Source: Ann Clin Transl NeurolDipòsit Digital de Documents de la UABUniversitat Autònoma de BarcelonaAnnals of Clinical and Translational Neurology, Vol 12, Iss 6, Pp 1201-1213 (2025)

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Academic Journal

Emerging role of ARHGAP29 in melanoma cell phenotype switching

Subjects: ARHGAP29; malignant melanoma; mesenchymal‐like phenotype

  • Source: Molecular Oncology, Vol 20, Iss 2, Pp 348-368 (2026)

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Academic Journal

Current Insights Into Individualized Diagnosis and Treatment of Allergic Rhinitis Based on Phenotype and Endotype

Subjects: allergic rhinitis; clinical treatment; endotype

  • Source: World Journal of Otorhinolaryngology-Head and Neck Surgery, Vol 12, Iss 1, Pp 124-135 (2026)

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Academic Journal

Resource manipulation reveals interactive phenotype-dependent foraging in free-ranging lizards

Subjects: Ecology; Ekologi; Zoology

  • Source: Journal of Animal Ecology. 93:1108-1122

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Academic Journal

Blended phenotype of TECPR2‐associated hereditary sensory‐autonomic neuropathy and Temple syndrome

Subjects: Male; Case Study; Facies

  • Source: Ann Clin Transl NeurolAnnals of Clinical and Translational Neurology, Vol 12, Iss 2, Pp 448-451 (2025)

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Academic Journal

Topological Distribution of KCNH2 Variants and Genotype‐Phenotype Relationship in Patients With Long QT Syndrome

Subjects: Male; ERG1 Potassium Channel; Long QT Syndrome

  • Source: Pacing and Clinical Electrophysiology. 48:351-362

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Academic Journal

MUC4 mutations promote a thrombotic phenotype in patients with paroxysmal nocturnal haemoglobinuria by increasing the deposition of terminal complement.

  • Authors : Chen Y; Department of Hematology, Tianjin Medical University General Hospital, Tianjin, China.; Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin, China.

Subjects: Hemoglobinuria, Paroxysmal*/Hemoglobinuria, Paroxysmal*/Hemoglobinuria, Paroxysmal*/genetics ; Hemoglobinuria, Paroxysmal*/Hemoglobinuria, Paroxysmal*/Hemoglobinuria, Paroxysmal*/complications ; Thrombosis*/Thrombosis*/Thrombosis*/genetics

  • Source: Clinical and translational medicine [Clin Transl Med] 2026 Jan; Vol. 16 (1), pp. e70567.Publisher: Wiley Country of Publication: United States NLM ID: 101597971 Publication Model: Print Cited Medium: Internet

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Academic Journal

Heterozygous variants in AP4S1 are not associated with a neurological phenotype

Subjects: Male; Adult; Heterozygote

  • Source: Ann Clin Transl NeurolAnnals of Clinical and Translational Neurology, Vol 12, Iss 4, Pp 851-854 (2025)

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Academic Journal

Effects of a bioengineered allogeneic cellular construct on burn‐related macrophage phenotype

Subjects: Lipopolysaccharides; Wound Healing; Phenotype

  • Source: Wound Repair and Regeneration. 32:992-1007

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Academic Journal

BCS1L‐Associated Disease: 5′‐UTR Variant Shifts the Phenotype Towards Axonal Neuropathy

Subjects: Research Article

  • Source: Ann Clin Transl Neurol

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  • 1-10 ل  61,804 نتائج ل ""Phenotype""