Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty

Evaluation of Immortalized AVPV- and Arcuate-Specific Neuronal Kisspeptin Cell Lines to Elucidate Potential Mechanisms of Estrogen Responsiveness and Temporal Gene Expression in Females

(2016) Dakota C. Jacobs et al.   ENDOCRINOLOGY

Causes, diagnosis, and treatment of central precocious puberty

(2016) Ana Claudia Latronico et al.   Lancet Diabetes & Endocrinology

Pubertal development and regulation

(2016) Ana Paula Abreu et al.   Lancet Diabetes & Endocrinology

Rbpj-κ mediated Notch signaling plays a critical role in development of hypothalamic Kisspeptin neurons

(2015) Matthew J. Biehl et al.   DEVELOPMENTAL BIOLOGY

Origin and dynamics of admixture in Brazilians and its effect on the pattern of deleterious mutations

(2015) Fernanda S. G. Kehdy et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Serum DLK1 is a potential prognostic biomarker in patients with hepatocellular carcinoma

(2015) Hong Li et al.   TUMOR BIOLOGY

MKRN3 Mutations in Familial Central Precocious Puberty

(2014) Felix Schreiner et al.   Hormone Research in Paediatrics

A novel MKRN3 missense mutation causing familial precocious puberty

(2014) L. de Vries et al.   HUMAN REPRODUCTION

Central Precocious Puberty in a Girl and Early Puberty in Her Brother Caused by a Novel Mutation in theMKRN3Gene

(2014) Nikolaos Settas et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Central Precocious Puberty That Appears to Be Sporadic Caused by Paternally Inherited Mutations in the Imprinted Gene Makorin Ring Finger 3

(2014) Delanie B. Macedo et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Detection of Delta-like 1 ligand for the diagnosis of tuberculous meningitis: An effective and rapid diagnostic method

(2014) Tao Peng et al.   JOURNAL OF INTERNATIONAL MEDICAL RESEARCH

Temple syndrome: improving the recognition of an underdiagnosed chromosome 14 imprinting disorder: an analysis of 51 published cases

(2014) Yiannis Ioannides et al.   JOURNAL OF MEDICAL GENETICS

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

(2014) John R. B. Perry et al.   NATURE

The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome

(2014) Yonatan Stelzer et al.   NATURE GENETICS

Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3

(2013) Ana Paula Abreu et al.   NEW ENGLAND JOURNAL OF MEDICINE

Pituitary Phenotypes of Mice Lacking the Notch Signalling Ligand Delta-Like 1 Homologue

(2012) L. Y. M. Cheung et al.   JOURNAL OF NEUROENDOCRINOLOGY

DLK1 Is a Somato-Dendritic Protein Expressed in Hypothalamic Arginine-Vasopressin and Oxytocin Neurons

(2012) Carine Villanueva et al.   PLoS One

Regulation of Notch1 signaling by delta-like ligand 1 intracellular domain through physical interaction

(2011) Jane Jung et al.   MOLECULES AND CELLS

The evolutionary biology of child health

(2011) B. Crespi   PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES

Mutations of theKISS1Gene in Disorders of Puberty

(2010) L. G. Silveira et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Transfers and transitions: Parent-offspring conflict, genomic imprinting, and the evolution of human life history

(2009) D. Haig   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes

(2008) Masayo Kagami et al.   NATURE GENETICS

AGPR54-Activating Mutation in a Patient with Central Precocious Puberty

(2008) Milena Gurgel Teles et al.   NEW ENGLAND JOURNAL OF MEDICINE