Cdkn1c Boosts the Development of Brown Adipose Tissue in a Murine Model of Silver Russell Syndrome

Paternally Inherited IGF2 Mutation and Growth Restriction

(2015) Matthias Begemann et al.   NEW ENGLAND JOURNAL OF MEDICINE

Paternal allelic mutation at theKcnq1locus reduces pancreatic β-cell mass by epigenetic modification ofCdkn1c

(2015) Shun-ichiro Asahara et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A Novel Variant inCDKN1CIs Associated With Intrauterine Growth Restriction, Short Stature, and Early-Adulthood-Onset Diabetes

(2014) Sarah L. Kerns et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Silver–Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C

(2014) Shinichi Nakashima et al.   JOURNAL OF HUMAN GENETICS

CDKN1C mutations: two sides of the same coin

(2014) Thomas Eggermann et al.   TRENDS IN MOLECULAR MEDICINE

Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth

(2013) KJ Jacob et al.   CLINICAL GENETICS

CDKN1Cmutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome

(2013) F Brioude et al.   JOURNAL OF MEDICAL GENETICS

Brown and beige fat: development, function and therapeutic potential

(2013) Matthew Harms et al.   NATURE MEDICINE

Increased Protein Stability of CDKN1C Causes a Gain-of-Function Phenotype in Patients with IMAGe Syndrome

(2013) Naoki Hamajima et al.   PLoS One

Beige Adipocytes Are a Distinct Type of Thermogenic Fat Cell in Mouse and Human

(2012) Jun Wu et al.   CELL

p57kip2 regulates glial fate decision in adult neural stem cells

(2012) J. J. Jadasz et al.   DEVELOPMENT

DNA Methylation Patterns in Cord Blood DNA and Body Size in Childhood

(2012) Caroline L. Relton et al.   PLoS One

Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver-Russell syndrome

(2011) Adriano Bonaldi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Silver-Russell syndrome

(2011) E. L. Wakeling   ARCHIVES OF DISEASE IN CHILDHOOD

Prdm16 is a physiologic regulator of hematopoietic stem cells

(2011) F. Aguilo et al.   BLOOD

Lung Stem Cell Self-Renewal Relies on BMI1-Dependent Control of Expression at Imprinted Loci

(2011) Sima J. Zacharek et al.   Cell Stem Cell

p57 Is Required for Quiescence and Maintenance of Adult Hematopoietic Stem Cells

(2011) Akinobu Matsumoto et al.   Cell Stem Cell

The Cyclin-Dependent Kinase Inhibitor p57Kip2 Regulates Cell Cycle Exit, Differentiation, and Migration of Embryonic Cerebral Cortical Precursors

(2011) Anna Tury et al.   CEREBRAL CORTEX

Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome

(2011) S. J. Tunster et al.   Disease Models & Mechanisms

The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases

(2011) Nicoletta Chiesa et al.   HUMAN MOLECULAR GENETICS

Ferreting out stem cells from their niches

(2011) Elaine Fuchs et al.   NATURE CELL BIOLOGY

Prdm16 determines the thermogenic program of subcutaneous white adipose tissue in mice

(2010) Patrick Seale et al.   JOURNAL OF CLINICAL INVESTIGATION

Epigenotype-phenotype correlations in Silver-Russell syndrome

(2010) E. L. Wakeling et al.   JOURNAL OF MEDICAL GENETICS

Prdm16 promotes stem cell maintenance in multiple tissues, partly by regulating oxidative stress

(2010) Sergei Chuikov et al.   NATURE CELL BIOLOGY

Beige Can Be Slimming

(2010) J. Ishibashi et al.   SCIENCE

Cold stimulates the behavioral response to hypoxia in newborn mice

(2009) Bieke Bollen et al.   AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY

Identification of novel regulators of hematopoietic stem cell development through refinement of stem cell localization and expression profiling

(2009) M. I. Mascarenhas et al.   BLOOD

p57Kip2 is a repressor of Mash1 activity and neuronal differentiation in neural stem cells

(2009) B Joseph et al.   CELL DEATH AND DIFFERENTIATION

Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regions

(2009) J. Bliek et al.   European Journal of Medical Genetics

Chronic Peroxisome Proliferator-activated Receptor γ (PPARγ) Activation of Epididymally Derived White Adipocyte Cultures Reveals a Population of Thermogenically Competent, UCP1-containing Adipocytes Molecularly Distinct from Classic Brown Adipocytes

(2009) Natasa Petrovic et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The Imprinted Phlda2 Gene Regulates Extraembryonic Energy Stores

(2009) S. J. Tunster et al.   MOLECULAR AND CELLULAR BIOLOGY

Distinct Developmental Roles of Cell Cycle Inhibitors p57Kip2 and p27Kip1 Distinguish Pituitary Progenitor Cell Cycle Exit from Cell Cycle Reentry of Differentiated Cells

(2009) S. Bilodeau et al.   MOLECULAR AND CELLULAR BIOLOGY

The Origins of Brown Adipose Tissue

(2009) Sven Enerbäck   NEW ENGLAND JOURNAL OF MEDICINE

Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family

(2009) Laura Cardarelli et al.   PEDIATRIC AND DEVELOPMENTAL PATHOLOGY

Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype

(2008) Sarah T. South et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Huddling: Brown Fat, Genomic Imprinting and the Warm Inner Glow

(2008) David Haig   CURRENT BIOLOGY

PRDM16 controls a brown fat/skeletal muscle switch

(2008) Patrick Seale et al.   NATURE