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Blood|June 26, 2008
Dll4 activation of Notch signaling reduces tumor vascularity and inhibits tumor growthMarta Segarra, Cassin Kimmel Williams, Maria de la Luz Sierra, et al.
The Journal of Clinical Endocrinology and Metabolism|November 20, 2013
Differences in adiposity in Cushing syndrome caused by PRKAR1A mutations: clues for the role of cyclic AMP signaling in obesity and diagnostic implicationsEdra London, Anya Rothenbuhler, Maya Lodish, et al.
Blood|August 9, 2003
Selective expression of stromal-derived factor-1 in the capillary vascular endothelium plays a role in Kaposi sarcoma pathogenesisLei Yao, Ombretta Salvucci, Adela R Cardones, et al.
Pediatric Research|May 22, 2019
Lipoprotein particles in patients with pediatric Cushing disease and possible cardiovascular risksAngeliki Makri, Anita Cheung, Ninet Sinaii, et al.
Clinical and Translational Medicine|October 23, 2024
Single-nucleus and spatial transcriptomics of paediatric ovary: Molecular insights into the dysregulated signalling pathways underlying premature ovarian insufficiency in classic galactosemiaRaghuveer Kavarthapu, Hong Lou, Thang Pham, et al.
The Journal of Clinical Endocrinology and Metabolism|June 24, 2016
Bilateral Adrenal Hyperplasia as a Possible Mechanism for Hyperandrogenism in Women With Polycystic Ovary SyndromeEvgenia Gourgari, Maya Lodish, Meg Keil, et al.
Blood|March 6, 2010
The transcription factor Gfi1 regulates G-CSF signaling and neutrophil development through the Ras activator RasGRP1Maria de la Luz Sierra, Shuhei Sakakibara, Paola Gasperini, et al.
Biology of Reproduction|November 9, 2025
The Utility of Artificial Intelligence and Deep Learning to Automate and Accelerate Follicle Counts in Human Ovarian TissueAlena Arlova, Jacqueline C Yano Maher, Hannah Anvari, et al.
Endocrine-Related Cancer|February 11, 2012
KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndromeParaskevi Xekouki, Michael M Hatch, Lin Lin, et al.
Clinical Endocrinology|June 14, 2016
Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without primary aldosteronism but with ACTH-dependent aldosterone hypersecretionAmalia Sertedaki, Athina Markou, Dimitrios Vlachakis, et al.
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