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Renin Cell Development: Insights From Chromatin Accessibility and Single-Cell Transcriptomics.

Stromal Transcription Factor 21 Regulates Development of the Renal Stroma via Interaction with Wnt/β-Catenin Signaling.

Does History of Prematurity Prompt Blood Pressure Evaluations at Primary Care Visits

Benjamin D Kornfeld, Gal Finer, Laura E Banks, Liliana Bolanos, Adolfo J Ariza

Transcription Factor 21 Is Required for Branching Morphogenesis and Regulates the Gdnf-Axis in Kidney Development.

Shintaro Ide, Gal Finer, Yoshiro Maezawa, Tuncer Onay, Tomokazu Souma, Rizaldy Scott, Kana Ide, Yoshihiro Akimoto, Chengjin Li, Minghao Ye, Xiangmin Zhao, Yusuke Baba, Takuya Minamizuka, Jing Jin, Minoru Takemoto, Koutaro Yokote, Susan E Quaggin

Clinical Approach to Proximal Renal Tubular Acidosis in Children

Gal Finer, Daniel Landau

Race, obesity, and the renin-angiotensin-aldosterone system: treatment response in children with primary hypertension

Andrew M South, Lester Arguelles, Gal Finer, Craig B Langman

Fluid Management: Pharmacologic and Renal Replacement Therapies.

Eric L Wald, Gal Finer, Mary E McBride, Nguyenvu Nguyen, John M Costello, Conrad L Epting

Applicability of estimating glomerular filtration rate equations in pediatric patients: comparison with a measured glomerular filtration rate by iohexol clearance.

Fang Deng, Gal Finer, Shannon Haymond, Ellen Brooks, Craig B Langman

Hyperphosphatemic familial tumoral calcinosis: Response to acetazolamide and postulated mechanisms

Gal Finer, Heather E Price, Richard M Shore, Kenneth E White, Craig B Langman

Divergent roles of Smad3 and PI3-kinase in murine adriamycin nephropathy indicate distinct mechanisms of proteinuria and fibrogenesis

Gal Finer, H William Schnaper, Yashpal S Kanwar, Xiaoyan Liang, Herbert Y Lin, Tomoko Hayashida

A conceptual framework for the molecular pathogenesis of progressive kidney disease.

H William Schnaper, Susan C Hubchak, Constance E Runyan, James A Browne, Gal Finer, Xiaoying Liu, Tomoko Hayashida

Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9.

Ortal Barel, Stavit A Shalev, Rivka Ofir, Asi Cohen, Joel Zlotogora, Zamir Shorer, Galia Mazor, Gal Finer, Shareef Khateeb, Noam Zilberberg, Ohad S Birk