Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Six1 and Six4 are essential for Gdnf expression in the metanephric mesenchyme and ureteric bud formation, while Six1 deficiency alone causes mesonephric-tubule defects

13 Jan 2007

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetic and Kidney Cyst Diseases
Share to Renal and related cancers
Share to Renal cell carcinoma treatment

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17300925
DOI: 10.1016/j.mod.2007.01.002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Six1 and Six4 are essential for Gdnf expression in the metanephric mesenchyme and ureteric bud formation, while Six1 deficiency alone causes mesonephric-tubule defectsPMID 17300925Read ↗

Six2 Defines and Regulates a Multipotent Self-Renewing Nephron Progenitor Population throughout Mammalian Kidney DevelopmentSemantic proximity Read ↗

Gen1 mutation caused kidney hypoplasia and defective ureter-bladder connections in mice.Semantic proximity Read ↗

Disruption of Gen1 Causes Congenital Anomalies of the Kidney and Urinary Tract in Mice.Semantic proximity Read ↗

Six1 is required for the early organogenesis of mammalian kidney.Semantic proximity Read ↗

Genetic determination of nephrogenesis: the Pax/Eya/Six gene networkSemantic proximity Read ↗

Six2 and Wnt Regulate Self-Renewal and Commitment of Nephron Progenitors through Shared Gene Regulatory NetworksSemantic proximity Read ↗

SIX1 acts synergistically with TBX18 in mediating ureteral smooth muscle formationSemantic proximity Read ↗

Crucial and Overlapping Roles of Six1 and Six2 in Craniofacial DevelopmentSemantic proximity Read ↗

Differential regulation of mouse and human nephron progenitors by the Six family of transcriptional regulatorsSemantic proximity Read ↗

SIX2 and BMP4 mutations associate with anomalous kidney development.Semantic proximity Read ↗

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.Semantic proximity Read ↗

Six family genes--structure and function as transcription factors and their roles in development.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.