Related references
Note: Only part of the references are listed.Prevalence of clinical, pathological and molecular features of glomerular basement membrane nephropathy caused by COL4A3 or COL4A4 mutations: a systematic review
Andreas Matthaiou et al.
CLINICAL KIDNEY JOURNAL (2020)
Clinical and genetic variability of PAX2-related disorder in the Japanese population
Rini Rossanti et al.
JOURNAL OF HUMAN GENETICS (2020)
dbNSFP v4: a comprehensive database of transcript-specific functional predictions and annotations for human nonsynonymous and splice-site SNVs
Xiaoming Liu et al.
GENOME MEDICINE (2020)
Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children
Asaf Vivante et al.
PEDIATRIC NEPHROLOGY (2019)
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system
Jia Rao et al.
CLINICAL GENETICS (2019)
From Otic Induction to Hair Cell Production: Pax2EGFP Cell Line Illuminates Key Stages of Development in Mouse Inner Ear Organoid Model
Stacy A. Schaefer et al.
STEM CELLS AND DEVELOPMENT (2018)
Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females
Zuying Xu et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2017)
Pax2 keeps nephron progenitors on track
Andrea Aguilar
NATURE REVIEWS NEPHROLOGY (2017)
Repression of Interstitial Identity in Nephron Progenitor Cells by Pax2 Establishes the Nephron-Interstitium Boundary during Kidney Development
Natalie Naiman et al.
DEVELOPMENTAL CELL (2017)
Association of PAX2 and Other Gene Mutations with the Clinical Manifestations of Renal Coloboma Syndrome
Toshiya Okumura et al.
PLOS ONE (2015)
Pax genes: regulators of lineage specification and progenitor cell maintenance
Judith A. Blake et al.
DEVELOPMENT (2014)
Mutations in PAX2 Associate with Adult-Onset FSGS
Moumita Barua et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2014)
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database
Matthew Bower et al.
HUMAN MUTATION (2012)
Using protein design algorithms to understand the molecular basis of disease caused by protein-DNA interactions: the Pax6 example
Andreu Alibes et al.
NUCLEIC ACIDS RESEARCH (2010)
Prevalence of mutations in renal developmental genes in children with renal hypodysplasia:: Results of the ESCAPE study
Stefanie Weber et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2006)
The FoldX web server: an online force field
J Schymkowitz et al.
NUCLEIC ACIDS RESEARCH (2005)
UCSF chimera - A visualization system for exploratory research and analysis
EF Pettersen et al.
JOURNAL OF COMPUTATIONAL CHEMISTRY (2004)
Phosphorylation of Pax2 by the c-jun N-terminal kinase and enhanced Pax2-dependent transcription activation
Y Cai et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Share Paper
