[Cranial chordomas: their cytological and ultrastructural characteristics]

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Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12.

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Vestnik oftalmologii·2023

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Vestnik oftalmologii·2022

[The specialized medical care of children with rare diseases].

Problemy sotsial'noi gigieny, zdravookhraneniia i istorii meditsiny·2022

Mucopolysaccharidosis Type I in the Russian Federation and Other Republics of the Former Soviet Union: Molecular Genetic Analysis and Epidemiology.

Frontiers in molecular biosciences·2022

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Arkhiv patologii·2026

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[Extrapulmonary lymphangioleiomyomatosis with retroperitoneal lymph node involvement].

Arkhiv patologii·2026

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Arkhiv patologii·2026

[Intraductal oncocytic papillary neoplasm of the pancreas].

Arkhiv patologii·2026

[A sealing agent for preserving anatomical specimens].

Arkhiv patologii·2026

Imbalanced p53-RB signaling triggers cGAS-STING-mediated immune activation in early oral cancer development.

Oncogene·2026

Research advances in the recurrence patterns of glioblastoma.

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IGF2BP3 promotes esophageal squamous cell carcinoma progression by regulating global protein translation.

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ATF4 and FGFR4 cooperatively support thyroid cancer progression and CAF-associated tumor-promoting features.

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DLL3 serves as a pivotal hub bridging malignant progression and immunosuppression in NECC with therapeutic implications validated via the organoid-TIL co-culture system.

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[Cranial chordomas: their cytological and ultrastructural characteristics]

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[Modern approaches to the diagnosis and treatment of Dravet syndrome in the Russian Federation. (Literature review and resolution of the Expert Council)].

Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12.

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[Cranial chordomas: their cytological and ultrastructural characteristics]

Abstract:

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