Search Results

Escape from X-chromosome inactivation and sex differences in Alzheimer's disease.

• Authors : Song, Qing-Hua; Zhao, Ke-Xuan; Huang, Shuai

Subjects: ALZHEIMER'S disease; X chromosome; PLANT embryology

• Source: Reviews in the Neurosciences; Apr2024, Vol. 35 Issue 3, p341-354, 14p

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Late diagnosis of the X-linked MCT8 deficiency (Allan–Herndon–Dudley syndrome) in a teenage girl with primary ovarian insufficiency.

• Authors : Sriram, Swetha; Shahid, Nabiha; Mysliwiec D, Diana

• Source: Journal of Pediatric Endocrinology & Metabolism; Apr2024, Vol. 37 Issue 4, p371-374, 4p

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X-chromosome linked genes associated with myeloid cell CNS trafficking contributes to female–male differences in the disease outcome for neuroinflammatory diseases.

• Authors : Darchiashvili, Sopiko; Kulkarni, Ratuja; Tandon, Ritesh

Subjects: MYELOID cells; CENTRAL nervous system injuries; AUTOIMMUNE diseases

• Source: NeuroImmune Pharmacology & Therapeutics; Jun2024, Vol. 3 Issue 2, p71-95, 25p

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Factors influencing reduced penetrance and variable expressivity in X-linked dystonia-parkinsonism.

• Authors : Pozojevic, Jelena; von Holt, Björn-Hergen; Westenberger, Ana

• Source: Medizinische Genetik; Jun2022, Vol. 34 Issue 2, p97-102, 6p

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FTX promotes esophageal cancer progression and desensitizes esophageal cancer cells to ionizing radiation by microRNA-99a/b-3p/WEE1/ERCC1 axis.

• Authors : Xu, Yangjie; Huang, Chaoming; Mao, Zijuan

• Source: Oncologie (De Gruyter); Nov2024, Vol. 26 Issue 6, p969-982, 14p

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Exploring evolutionary trajectories in ovarian cancer patients by longitudinal analysis of ctDNA.

• Authors : Kutz, Oliver; Drukewitz, Stephan; Krüger, Alexander

Subjects: CIRCULATING tumor DNA; OVARIAN tumors; OVARIAN cancer

• Source: Clinical Chemistry & Laboratory Medicine; Sep2024, Vol. 62 Issue 10, p2070-2081, 12p

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The role of epigenetics in rare diseases.

• Authors : Horsthemke, Bernhard

Subjects: GENOMIC imprinting; EPIGENOMICS; EPIGENETICS

• Source: Medizinische Genetik; Jun2024, Vol. 36 Issue 2, p111-120, 10p

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Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions.

• Authors : Cai, Meiying; Chen, Xuemei; Li, Ying

Subjects: GENETIC mutation; PRENATAL diagnosis; GENETIC testing

• Source: Journal of Perinatal Medicine; Jan2024, Vol. 52 Issue 1, p96-101, 6p

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Polymorphisms of CYP17A1, CYP19, and androgen in Brazilian women with uterine leiomyomas.

• Authors : Rosa, Fabíola Encinas; Canevari, Renata de Azevedo; Ambrosio, Eliane Papa

Subjects: UTERINE fibroids; SMOOTH muscle tumors; TUMORSBRAZIL

• Source: Clinical Chemistry & Laboratory Medicine; Jun2008, Vol. 46 Issue 6, p814-823, 10p, 4 Charts, 2 Graphs

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The chromatin – triple helix connection.

• Authors : Maldonado, Rodrigo; Längst, Gernot

Subjects: GENE enhancers; RNA-binding proteins; CHROMATIN

• Source: Biological Chemistry; Oct2023, Vol. 404 Issue 11/12, p1037-1049, 13p

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