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TRIM32
Educational Paper Ciliopathies
Ciliopathiesneuromuscularciliopathies Disorders Disorders Ciliopathiesciliopathies
Ciliopathies Gene Panel
Detection of TRIM32 Deletions in LGMD Patients Analyzed by a Combined Strategy of CGH Array and Massively Parallel Sequencing
[Frontiers in Bioscience 13, 2633-2652, January 1, 2008] 2633 Intraflagellar Transport: from Molecular Characterisation to Mech
Molecular Diagnostic Requisition
The Limb-Girdle Muscular Dystrophies and the Dystrophinopathies Review Article
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
MKKS Is a Centrosome-Shuttling Protein Degraded by Disease
An EMT-Primary Cilium-GLIS2 Signaling Axis Regulates Mammogenesis and Claudin-Low Breast Tumorigenesis
Loss of the Bbsome Perturbs Endocytic Trafficking and Disrupts Virulence of Trypanosoma Brucei
E3 Ubiquitin Ligase TRIM Proteins, Cell Cycle and Mitosis
Ciliary Genes in Renal Cystic Diseases
MVL - Institutional & Self-Pay Test Price List *All Prices Are for Institutional Clients and Self-Pay ONLY
Download CGT Exome V2.0
The E3 Ligase TRIM32 Is an Effector of the RAS Family Gtpase RAP2
EGL Test Description
Lysine63-Linked Ubiquitin Chains Earmark Gpcrs for Bbsome
Top View
ADX609 3301 Athena Newborndx Gene Panel Update 3-30-20.Indd
Ciliopathies
Bardet–Biedl Syndrome: Beyond the Cilium
Kidneyseq™ V4 – 312 Genes CAKUT Branchiooculofacial Syndrome AD
Novel Compound Heterozygous BBS2 and Homozygous MKKS Variants Detected in Chinese Families with Bardet–Biedl Syndrome
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Functional Characterization of TRIM24 and TRIM32 Proteins in the Heart Through Their Interaction with Dysbindin
TRIM32: a Multifunctional Protein Involved in Muscle Homeostasis, Glucose Metabolism, and Tumorigenesis
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Nuclear Roles for Cilia-Associated Proteins
Tripartite-Motif Family Genes Associated with Cancer Stem Cells
Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families
Target Capture Sequencing for Inherited Retinal Degenerations
Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease
NGS Oncology)
Ciliopathies Gene Panel
EGL Test Description
DIAGNOSTIC GENETIC TESTING REQUISITION SPECIMENS: 1428 Madison Ave., Rm AB2-25, New York, NY 10029 MAIL: One Gustave L