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MKRN3
Protein Interaction Network of Alternatively Spliced Isoforms from Brain Links Genetic Risk Factors for Autism
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Egfr Activates a Taz-Driven Oncogenic Program in Glioblastoma
Genetic Testing in Inherited Endocrine Disorders
Enrichment Analyses of Diseases and Pathways Associated With
Mutations in the Maternally Imprinted Gene MKRN3 Are Common in Familial Central Precocious Puberty
Mutations in the Maternally Imprinted Gene MKRN3 Are Common in Familial Central Precocious Puberty
PWS Publications Apr to Jun 2020 PWS PAPERS of INTEREST
Conservation of Imprinting and Methylation of MKRN3, MAGEL2 and NDN Genes in Cattle
The Neurobiology of Mouse Models Syntenic to Human Chromosome 15Q
Genetic Dissection Identifies Necdin As a Driver Gene in a Mouse Model
MKRN3 Interacts with Several Proteins Implicated in Puberty Timing but Does Not Influence GNRH1 Expression
Dynamic Expression of Imprinted Genes in the Developing and Postnatal Pituitary Gland
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Genomic Analyses for Age at Menarche Identify 389 Independent Signals and Indicate BMI-Independent Effects of Puberty Timing on Cancer Susceptibility
MKRN3 Regulates the Epigenetic Switch of Mammalian Puberty Via
The MKRN3 Gene
De Novo Mutations Involved in Post-Transcriptional Dysregulation
Top View
MKRN3 Gene Makorin Ring Finger Protein 3
MKRN3 and KISS1R Mutations in Precocious and Early Puberty
Methylome Profiling of Healthy and Central Precocious Puberty Girls Danielle S
Flexible Model-Based Joint Probabilistic Clustering of Binary and Continuous Inputs and Its Application to Genetic Regulation and Cancer
A Case of Familial Central Precocious Puberty Caused by a Novel Mutation
Characterization of Global Loss of Imprinting in Fetal Overgrowth Syndrome Induced by Assisted Reproduction
Elevated Expression of MKRN3 in Squamous Cell Carcinoma of the Head and Neck and Its Clinical Signi Cance
Ventriculomegaly Precision Panel Overview Indications Clinical Utility
Developmental Gene Expression Differences Between Humans and Mammalian Models
Genetic Etiologies of Central Precocious Puberty and the Role of Imprinted Genes
Patients with PWS and Related Syndromes Display Differentially
Personalized Food Intervention and Therapy for Autism Spectrum Disorder Management Advances in Neurobiology
Elucidation and Validation of the Burden of DNA Variations in Autism Spectrum Disorders to Assess the Impact on the Genetic Pathways