The Agonist Activity of Tamoxifen Is Inhibited by the Short Heterodimer Partner Orphan Nuclear Receptor in Human Endometrial Cancer Cells [PDF]
, 2002 Carolyn M. Klinge +2 more
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Prioritising research on endocrine disruption in the marine environment: a global perspective
Biological Reviews, Volume 101, Issue 2, Page 848-868, April 2026.ABSTRACT A healthy ocean is a crucial life support system that regulates the global climate, is a source of oxygen and supports major economic activities. A vast and understudied biodiversity from micro‐ to macro‐organisms is integral to ocean health.
Patricia I. S. Pinto +23 more
wiley +1 more source
The Nuclear Orphan Receptor Nur77 Is a Lipotoxicity Sensor Regulating Glucose-Induced Insulin Secretion in Pancreatic β-Cells [PDF]
, 2012 Olivier Briand +12 more
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How the circadian nuclear orphan receptor REV-ERBα represses transcription: Temporal and spatial phase separation combined [PDF]
, 2023 Ueli Schibler
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Constitutive Activation of Retinoic Acid Receptor β2 Promoter by Orphan Nuclear Receptor TR2 [PDF]
, 2000 Li-Na Wei, Xinli Hu, Chatchai Chinpaisal
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Nuclear orphan receptor ERRα promotes cisplatin resistance in breast cancer cells by targeting CCNE2
, 2022 Jiahui Liu +16 more
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Post‐Translational Modifications in Animal Circadian Clocks
Advanced Science, Volume 13, Issue 16, 18 March 2026.Circadian clocks coordinate physiology with daily environmental cycles through conserved transcriptional–translational feedback loops. This review summarizes how post‐translational modifications fine‐tune clock function, highlights the evolutionary convergence of circadian timekeeping in Drosophila and mammals, and emphasizes the central of these ...
Xianhui Liu, Yong Zhang
wiley +1 more source
Solid Subtype of Papillary Thyroid Carcinoma: A Case Series Highlighting Aggressive Features
Clinical Case Reports, Volume 14, Issue 3, March 2026.Hematoxylin and eosin (H&E) stained section, 40×. Tumor cells with “Orphan Annie eye” nuclei arranged in solid nests. ABSTRACT Papillary thyroid carcinoma (PTC) is the most common malignant thyroid neoplasm. Its solid/trabecular subtype (STPTC) is rare, and its aggressiveness remains controversial.
Rafael Castellanos Bueno +4 more
wiley +1 more source
Developmental Dynamics, Volume 255, Issue 3, Page 228-245, March 2026.Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki +6 more
wiley +1 more source