Mice With a Conditional Deletion of Talpid3 ( KIAA0586 ) – A Model for Joubert Syndrome

Journal of Pathology - United States
doi 10.1002/path.5271
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

Joubert Syndrome: A Model for Untangling Recessive Disorders With Extreme Genetic Heterogeneity

Journal of Medical Genetics
Genetics
2015English

NPHP1 Gene Deletion Is a Rare Cause of Joubert Syndrome Related Disorders

Journal of Medical Genetics
Genetics
2005English

A New Mouse Model for the Neurodevelopmental Ciliopathy Joubert Syndrome

Journal of Pathology
Forensic MedicinePathology
2019English

Generation of Mice With Hepatocyte-Specific Conditional Deletion of Notum

PLoS ONE
Multidisciplinary
2016English

Joubert Syndrome With Ocular Defect

2020English

Joubert Syndrome: A Rare Cause for Developmental Delay

Journal of Medical Science And clinical Research
2017English

Modeling Sjögren's Syndrome With Id3 Conditional Knockout Mice

Immunology Letters
AllergyImmunology
2011English

Joubert Syndrome: A Rare Radiological Case

Cureus
2019English

Hippocampal and Visuospatial Learning Defects in Mice With a Deletion of Frizzled 9, a Gene in the Williams Syndrome Deletion Interval

Development (Cambridge)
Developmental BiologyMolecular Biology
2005English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy