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TTC7A
Exome Sequencing Identifies Mutations in the Gene TTC7A In
Primepcr™Assay Validation Report
The Capacity of Long-Term in Vitro Proliferation of Acute Myeloid
TTC7A Mutations Disrupt Intestinal Epithelial Apicobasal Polarity
CD98 [19] Among Others [5][23]
Tetratricopeptide Repeat Domain 7A Is a Nuclear Factor That Modulates
De Novo and Rare Mutations in the HSPA1L Heat
Novel Mutations of the Tetratricopeptide Repeat Domain 7A Gene and Phenotype/Genotype Comparison
Protein Tyrosine Phosphorylation in Haematopoietic Cancers and the Functional Significance of Phospho- Lyn SH2 Domain
A CASE of TTC7A DEFICIENCY Presented by Dr Bella Shadur Case
Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome
Book Halim.Indb
WO 2014/177699 Al 6 November 2014 (06.11.2014) P O P C T
TTC7A Mouse Monoclonal Antibody [Clone ID: OTI6D2] – TA812308
A Novel TTC7A Deficiency Presenting with Combined Immunodeficiency
Rescuing TTC7A Mutant Phenotypes Associated with Very Early Onset Inflammatory Bowel Disease Via High Throughput Drug Screening
Heterogeneity in Combined Immunodeficiencies with Associated Or Syndromic Features (Review)
Novel Exonic Deletions in TTC7A in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency
Top View
Supplementary Table 2. 503-‐Gene List Differentially Expressed
Primary T Cell Immunodeficiencies Associated with Disturbed Proximal
WO 2014/068408 A2 8 May 2014 (08.05.2014) P O P C T
Plasma Membrane Protein Identifications from Human Bone Marrow Mesenchymal Stem Cells
Stem Cell Transplantation for Tetratricopeptide Repeat Domain 7A Deficiency: Long-Term Follow Up
The E3 Ubiquitin Ligase UBR5 Interacts with TTC7A and May Be Associated with Very Early Onset Inflammatory Bowel Disease
(TTC7A) Mutations for Combined Immunodeficiency with Intestinal Atresias
Supplementary File 1B Revised-Förslag
A Novel Homozygous TTC7A Missense Mutation Results in Familial Multiple Intestinal Atresia and Combined Immunodefciency
Combining Genome Wide Association Studies and Differential Gene
Exome Sequencing of Fetal Anomaly Syndromes: Novel Phenotype–Genotype Discoveries
(TTC7A) Mutations for Combined Immunodeficiency with Intest
TTC7A Mouse Monoclonal Antibody [Clone ID: OTI1D4] Product Data
WO 2014/100434 Al 26 June 2014 (26.06.2014) W P O P C T
„Identification and Characterization of Interferon Induced Ubiquitinated
A Case of Severe Malnutrition Infant with Neonatal Onset Intractable Diarrhea Youhong Fang, Youyou Luo, Jindan Yu and Jie Chen*