Differentiation of human pluripotent stem cells into nephron progenitor cells in a serum and feeder free system

M Kang, YM Han - PloS one, 2014 - journals.plos.org
Objectives Kidney disease is emerging as a critical medical problem worldwide. Because of
limited treatment options for the damaged kidney, stem cell treatment is becoming an …

The role of PAX2 in neurodevelopment and disease

N Lv, Y Wang, M Zhao, L Dong… - … Disease and Treatment, 2021 - Taylor & Francis
In developmental biology, transcription factors are involved in regulating the process of
neural development, controlling the differentiation of nerve cells, and affecting the normal …

Signaling during kidney development

M Krause, A Rak-Raszewska, I Pietilä, SE Quaggin… - Cells, 2015 - mdpi.com
The kidney plays an essential role during excretion of metabolic waste products,
maintenance of key homeostasis components such as ion concentrations and hormone …

Nephron number, hypertension, and CKD: physiological and genetic insight from humans and animal models

X Wang, MR Garrett - Physiological Genomics, 2017 - journals.physiology.org
The kidneys play a vital role in the excretion of waste products and the regulation of
electrolytes, maintenance of acid–base balance, regulation of blood pressure, and …

Ouabain protects against adverse developmental programming of the kidney

J Li, GR Khodus, M Kruusmägi, P Kamali-Zare… - Nature …, 2010 - nature.com
The kidney is extraordinarily sensitive to adverse fetal programming. Malnutrition, the most
common form of developmental challenge, retards the formation of functional units, the …

Anatomy and histology of the lower urinary tract

W Pradidarcheep, C Wallner, NF Dabhoiwala… - Urinary Tract, 2011 - Springer
The function of the lower urinary tract is basically storage of urine in the bladder and the at-
will periodic evacuation of the stored urine. Urinary incontinence is one of the most common …

Developmental genetics and congenital anomalies of the kidney and urinary tract

N Uy, K Reidy - Journal of pediatric genetics, 2016 - thieme-connect.com
Congenital anomalies of the kidney and urinary tract (CAKUT) are common birth defects and
the leading cause of end-stage renal disease in children. There is a wide spectrum of renal …

Association of PAX2 and other gene mutations with the clinical manifestations of renal coloboma syndrome

T Okumura, K Furuichi, T Higashide, M Sakurai… - PLoS …, 2015 - journals.plos.org
Background Renal coloboma syndrome (RCS) is characterized by renal anomalies and
optic nerve colobomas. PAX2 mutations contribute to RCS. However, approximately half of …

HDAC inhibitors in kidney development and disease

LL Brilli, LM Swanhart, MP de Caestecker… - Pediatric …, 2013 - Springer
The discovery that histone deacetylase inhibitors (HDACis) can attenuate acute kidney
injury (AKI)-mediated damage and reduce fibrosis in kidney disease models has opened the …

Primary cultures of glomerular parietal epithelial cells or podocytes with proven origin

N Kabgani, T Grigoleit, K Schulte, A Sechi… - PloS one, 2012 - journals.plos.org
Parietal epithelial cells (PECs) are crucially involved in the pathogenesis of rapidly
progressive glomerulonephritis (RPGN) as well as in focal and segmental …