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POLR1D
POLR1D Gene RNA Polymerase I and III Subunit D
Aneuploidy: Using Genetic Instability to Preserve a Haploid Genome?
The Roles of RNA Polymerase I and III Subunits Polr1a, Polr1c, and Polr1d in Craniofacial Development BY
POLR1B and Neural Crest Cell Anomalies in Treacher Collins Syndrome Type 4
A Novel Familial Mutation Associated with Treacher Collins Syndrome: a Case Report
Identification of Shared and Unique Gene Families Associated with Oral
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
Dissecting the Genetics of Human Communication
Supplementary Table 1 Double Treatment Vs Single Treatment
Genetic Amplification of the NOTCH Modulator LNX2 Upregulates The
Ribosomal Proteins and Human Diseases: Molecular Mechanisms and Targeted Therapy ✉ Jian Kang1,2, Natalie Brajanovski1, Keefe T
POLR1D (NM 001206559) Human Tagged ORF Clone Product Data
A Network Inference Approach to Understanding Musculoskeletal
High-Density Array Comparative Genomic Hybridization Detects Novel Copy Number Alterations in Gastric Adenocarcinoma
INFIMA Leverages Multi-Omics Model Organism Data to Identify Effector Genes of Human GWAS Variants
Assessing Mitochondrial Theory of Aging on the Transcriptome Level
Autosomal Recessive POLR1D Mutation with Decrease of TCOF1 Mrna Is Responsible for Treacher Collins Syndrome
RNA-Seq Analysis of Tgfβ3 Mice Ozturk Et Al
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Supplementary Material Peptide-Conjugated Oligonucleotides Evoke Long-Lasting Myotonic Dystrophy Correction in Patient-Derived C
Product Description SALSA® MLPA® Probemix P310-B4 TCOF1 to Be Used with the MLPA General Protocol
Mapping the Transcriptomics Landscape of Post-Traumatic Stress
Screening Key Genes and Signaling Pathways in Colorectal Cancer by Integrated Bioinformatics Analysis
Genetic Amplification of the NOTCH Modulator LNX2 Upregulates The
Beyond Treacher Collins Syndrome
Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
POLR1D (NM 015972) Human Tagged ORF Clone Product Data
Recessive Mutations in POLR1C Cause a Leukodystrophy by Impairing Biogenesis of RNA Polymerase III
Download Validation Data
POLR1D (NM 015972) Human Recombinant Protein – TP301466 | Origene
Cell-Free DNA Analysis Reveals POLR1D-Mediated Resistance To
Identification of Hub Genes in Different Stages of Colorectal Cancer
Clinical Spectrum of POLR3-Related Leukodystrophy Caused by Biallelic POLR1C Pathogenic Variants
Extreme Manifestation of a Familial Case of Treacher Collins Syndrome in an Infant with Arhinia, Eyelid Colobomas and Single Kidney
Genetic Investigation and Clinical Aspects in a Romanian Treacher
POLR1D (NM 152705) Human Recombinant Protein Product Data
Identification of Candidate Biomarkers and Pathways Associated with Type 1 Diabetes Mellitus Using Bioinformatics Analysis