DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» NSD1
NSD1
Epigenetic Modifications Precede Molecular Alterations and Drive Human Hepatocarcinogenesis
Novel Pharmacological Maps of Protein Lysine Methyltransferases: Key for Target Deorphanization Obdulia Rabal* , Andrea Castellar and Julen Oyarzabal*
Treatments for Ankyloglossia and Ankyloglossia with Concomitant Lip-Tie Comparative Effectiveness Review Number 149
Sequence Specificity Analysis of the SETD2 Protein Lysine Methyltransferase and Discovery of a SETD2 Super-Substrate
NSD1) Methyltransferase in Coordinating Lysine 36 Methylation at Histone 3 with RNA Polymerase II Function
Genetics of Lipedema: New Perspectives on Genetic Research and Molecular Diagnoses S
Prioritization of Candidate Disease Genes by Topological Similarity
Cerebrovascular Diseases in Two Patients with Entire NSD1 Deletion
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
Epigenome Dysregulation Resulting from NSD1 Mutation in Head and Neck Squamous Cell
Lmx1b-Targeted Cis-Regulatory Modules Involved in Limb Dorsalization Endika Haro1, Billy A
NSD1 Sirna (H): Sc-45612
Epigenetic Inactivation of the Sotos Overgrowth Syndrome Gene Histone Methyltransferase NSD1 in Human Neuroblastoma and Glioma
Role for the Nuclear Receptor-Binding SET Domain Protein 1 (NSD1) Methyltransferase in Coordinating Lysine 36 Methylation at Histone 3 with RNA Polymerase II Function
Sotos Syndrome
Abstracts from the 50Th European Society of Human Genetics Conference: Oral Presentations
Epigenome Dysregulation Resulting from NSD1 Mutation in Head and Neck Squamous Cell Carcinoma
Sotos Syndrome (Nsd1) Deletion/Duplication
Top View
Autism Genepheno: Text Mining of Gene-Phenotype Associations Reveals New Phenotypic Profiles of Autism-Associated Genes
Using the Zebrafish to Investigate the Role of the Nup98-Nsd1 Oncogene and Loss of Nup98 in High-Risk Pediatric Acute Myeloid Leukemia
NSD1 (NM 022455) Human Tagged ORF Clone Product Data
Mouse Nsd1 Conditional Knockout Project (CRISPR/Cas9)
Download Product Insert (PDF)
Familial Sotos Syndrome Caused by a Novel Missense Mutation, C2175S
Mutations in NSD1 Are Responsible for Sotos Syndrome, but Are Not a Frequent Finding in Other Overgrowth Phenotypes
NSD1 Inactivation Defines an Immune Cold, DNA Hypomethylated Subtype
Spectrum of NSD1 Mutations in Sotos and Weaver Syndromes
NSD1 Inactivation Defines an Immune Cold, DNA Hypomethylated Subtype in Squamous Cell
Atlas Journal
BMC Medical Genomics Biomed Central
A Genome-Wide DNA Methylation Signature for SETD1B-Related Syndrome I
NSD1: a Lysine Methyltransferase Between Developmental Disorders and Cancer
5Q35 Duplications FTNW.Pdf
Histone H3 Tail Binds a Unique Sensing Pocket in EZH2 to Activate the PRC2 Methyltransferase
Disruption of NSD1 in Head and Neck Cancer Promotes Favorable Chemotherapeutic Responses Linked to Hypomethylation
Product Description SALSA® MLPA® Probemix P026-E2 Sotos to Be Used with the MLPA General Protocol