Further delineation of the SATB2 phenotype

Expression of Transcription Factor Satb2 in Adult Mouse Brain

(2014) Ying Huang et al.   Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology

SATB2 is a novel marker of osteoblastic differentiation in bone and soft tissue tumours

(2013) James R Conner et al.   HISTOPATHOLOGY

Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene

(2013) Petcharat Leoyklang et al.   HUMAN GENETICS

From neural development to cognition: unexpected roles for chromatin

(2013) Jehnna L. Ronan et al.   NATURE REVIEWS GENETICS

Bmp and Shh Signaling Mediate the Expression of satb2 in the Pharyngeal Arches

(2013) Kelly Sheehan-Rooney et al.   PLoS One

Effects of a miR-31, Runx2, and Satb2 Regulatory Loop on the Osteogenic Differentiation of Bone Mesenchymal Stem Cells

(2013) Yuan Deng et al.   STEM CELLS AND DEVELOPMENT

A cohort study of the prognostic and treatment predictive value of SATB2 expression in colorectal cancer

(2012) J Eberhard et al.   BRITISH JOURNAL OF CANCER

Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

(2012) Michael E. Talkowski et al.   CELL

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

(2012) Anita Rauch et al.   LANCET

Decreased Expression of SATB2: A Novel Independent Prognostic Marker of Worse Outcome in Laryngeal Carcinoma Patients

(2012) Tian-Run Liu et al.   PLoS One

Protooncogene Ski cooperates with the chromatin-remodeling factor Satb2 in specifying callosal neurons

(2012) C. Baranek et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A network of genetic repression and derepression specifies projection fates in the developing neocortex

(2012) K. Srinivasan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome region

(2012) Susana Ferreira et al.   Molecular Cytogenetics

In-depth annotation of SNPs arising from resequencing projects using NGS-SNP

(2011) J. R. Grant et al.   BIOINFORMATICS

Satb2, modularity, and the evolvability of the vertebrate jaw

(2011) Jennifer L. Fish et al.   EVOLUTION & DEVELOPMENT

Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype

(2011) M. Balasubramanian et al.   JOURNAL OF MEDICAL GENETICS

Ensembl 2012

(2011) P. Flicek et al.   NUCLEIC ACIDS RESEARCH

Common Variants in a Novel Gene, FONG on Chromosome 2q33.1 Confer Risk of Osteoporosis in Japanese

(2011) Ikuyo Kou et al.   PLoS One

The refinement of the critical region for the 2q31.2q32.3 deletion syndrome indicates candidate genes for mental retardation and speech impairment

(2010) Alessandro Cocchella et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

A cross-species analysis of Satb2 expression suggests deep conservation across vertebrate lineages

(2010) Kelly Sheehan-Rooney et al.   DEVELOPMENTAL DYNAMICS

A network connecting Runx2, SATB2, and the miR-23a 27a 24-2 cluster regulates the osteoblast differentiation program

(2010) M. Q. Hassan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The Sequence Alignment/Map format and SAMtools

(2009) H. Li et al.   BIOINFORMATICS

The mRNA expression of SATB1 and SATB2 in human breast cancer

(2009) Neill Patani et al.   Cancer Cell International

Toriello-Carey syndrome in a patient with ade novobalanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2

(2009) DH Tegay et al.   CLINICAL GENETICS

Another patient with a de novo deletion further delineates the 2q33.1 microdeletion syndrome

(2009) Thomy J. de Ravel et al.   European Journal of Medical Genetics

4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate

(2009) Jill Urquhart et al.   European Journal of Medical Genetics

Down-regulated expression of SATB2 is associated with metastasis and poor prognosis in colorectal cancer

(2009) Shuang Wang et al.   JOURNAL OF PATHOLOGY

Small Deletions of SATB2 Cause Some of the Clinical Features of the 2q33.1 Microdeletion Syndrome

(2009) Jill A. Rosenfeld et al.   PLoS One

SATB2 interacts with chromatin-remodeling molecules in differentiating cortical neurons

(2008) Andrea B. Gyorgy et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Satb2 Is a Postmitotic Determinant for Upper-Layer Neuron Specification in the Neocortex

(2008) Olga Britanova et al.   NEURON

Satb2 Regulates Callosal Projection Neuron Identity in the Developing Cerebral Cortex

(2008) Elizabeth A. Alcamo et al.   NEURON