DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» TGM6
TGM6
Genomic Variants Reveal Differential Evolutionary Constraints on Human Transglutaminases and Point Towards Unrecognized Significance of Transglutaminase 2
TGM6 L517W Is Not a Pathogenic Variant for Spinocerebellar Ataxia Type 35
Neurologic Outcomes in Friedreich Ataxia: Study of a Single-Site Cohort E415
Gene Ontology Functional Annotations and Pleiotropy
Comprehensive Comparison of Three Commercial Human Whole-Exome
Genetic Background of Ataxia in Children Younger Than 5 Years in Finland E444
W O 2019/200163 Al 17 October 2019 (17.10.2019) W IPO I PCT
Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma
Network Analysis of Potential Risk Genes for Psoriasis Huilin Wang, Wenjun Chen, Jin He, Wenjuan Xu and Jiangwei Liu*
Transglutaminase 3: the Involvement in Epithelial Differentiation and Cancer
Molecular Genetic Studies of Recessively Inherited Eye Diseases
TGM5 Gene Transglutaminase 5
Diverse Noncoding Mutations Contribute to Deregulation of Cis-Regulatory Landscape in Pediatric Cancers
This Thesis Has Been Submitted in Fulfilment of the Requirements for a Postgraduate Degree (E.G
TGM6 Antibody
1 Imipramine Treatment and Resiliency Exhibit Similar
Cancer Classes of Tumors Beyond Tissue of Origin Agustín González-Reymúndez1,2 & Ana I
Efficient Mapping of Transgene Integration Sites and Local Structural
Top View
Lentivirus-Mediated RNA Interference Targeting FAMLF-1 Inhibits Cell
Characterization of Ataxin-2 and Its Interaction Partners
Anti-TGM5 Antibody (ARG41106)
Unmasking Adrenoleukodystrophy in a Cohort of Cerebellar Ataxia
PDF) S2 Table
In Trans Variant Calling Reveals Enrichment for Compound Heterozygous Variants in Genes Involved in Neuronal Development and Growth
The Long Tail and Rare Disease Research: the Impact of Next-Generation Sequencing for Rare Mendelian Disorders
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force
A Brief Review on Spinocerebellar Ataxia and Its Treatment Journal of Neurology Research Reviews & Reports
Targeted Next-Generation Resequencing Panel in Inherited Ataxias
A Significant Inflation in TGM6 Genetic Risk Casts Doubt in Its Causation In
Dissertation
Targeted Next-Generation Sequencing Identifies Novel Variants in Candidate Genes for Parkinson’S Disease in Black South African and Nigerian Patients Oluwafemi G
Ataxic Disorders
Impact of Exome Sequencing in Characterizing Mendelian Disorders
Molecular Genetic Testing in Clinical Diagnostic Assessments That Demonstrate Correlations in Patients with Autosomal Recessive Inherited Retinal Dystrophy
The Ratio of Exhausted to Resident Infiltrating Lymphocytes Is Prognostic for Colorectal Cancer Patient Outcome
Autoimmune Encephalitis History & Current Knowledge