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Everything about TBCD
Protein-coding gene in the species Homo sapiens
Tubulin-specific chaperone D is a protein that in humans is encoded by the TBCD gene. Wikipedia →
🧭 Start here: a 6-step reading path
- Read the overview: TBCDA 5-minute orientation
- Skim a recent paper: PEBAT, an Intriguing Neurodegenerative Tubulinopathy Caused by a Novel Homozygous Variant in TBCD: A Case Series and Literature ReviewInfluential work since 2022
- Read the landmark paper: Biallelic Mutations in TBCD , Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset EncephalopathyCited 79 times
- Go sideways: TBCEA closely related topic
- Go sideways: TBCAA closely related topic
📖 Definitions
No dictionary entry for this exact phrase.
🗂️ The subject at a glance
🏆 Landmark papers (most cited)
Biallelic Mutations in TBCD , Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy
Biallelic TBCD Mutations Cause Early-Onset Neurodegenerative Encephalopathy
A Trimer Consisting of the Tubulin-specific Chaperone D (TBCD), Regulatory GTPase ARL2, and β-Tubulin Is Required for Maintaining the Microtubule Network
Effect of TBCD and its regulatory interactor Arl2 on tubulin and microtubule integrity
Crystal electric field excitations in the quasicrystal approximantTbCd6studied by inelastic neutron scattering
Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone‐mediated tubulinopathy
TBCD Links Centriologenesis, Spindle Microtubule Dynamics, and Midbody Abscission in Human Cells
Nucleotide Binding to ARL2 in the TBCD ∙ ARL2 ∙ β-Tubulin Complex Drives Conformational Changes in β-Tubulin
🆕 Influential since 2022
PEBAT, an Intriguing Neurodegenerative Tubulinopathy Caused by a Novel Homozygous Variant in TBCD: A Case Series and Literature Review
CRISPR/Cas9 and piggyBac Transposon-Based Conversion of a Pathogenic Biallelic TBCD Variant in a Patient-Derived iPSC Line Allows Correction of PEBAT-Related Endophenotypes
TUBULİN-SPECİFİC CHAPERONE D (TBCD) GENİNDE YENİ BİR MUTASYON TESPİT EDİLEN PEBAT SENDROMLU OLGU
A Variant in TBCD Associated with Motoneuronopathy and Corpus Callosum Hypoplasia: A Case Report
Combined homozygous HACE1 and TBCD variants in two siblings with severe early-onset neurodevelopmental disorder: Two case reports
📚 Books worth reading
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🔗 Related topics
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- PFDN4 Prefoldin subunit 4 is a protein that in humans is encoded by the PFDN4 gene. This gene encodes a member of the prefoldin beta subunit family. The encoded…
- Tubulin beta-4B chain Tubulin beta-4B chain formerly known as tubulin beta-2C chain is a protein that in humans is encoded by the TUBB4B gene. It is thought that this protein…
- ARL2 ADP-ribosylation factor-like protein 2 is a protein that in humans is encoded by the ARL2 gene. The ADP-ribosylation factor (ARF) genes are small GTP-binding…
- TUBA1B Tubulin alpha-1B chain is a protein that in humans is encoded by the TUBA1B gene. TUBA1B has been shown to interact with PIK3R1. Antibodies against tubulin…
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