Cell Signaling Technology

Acetyl-alpha-Tubulin (Lys40) (D20G3) Rabbit Monoclonal Antibody (Alexa Fluor® 488 Conjugate)

#35652 · $187

19
Citing papers
603
Combined citations
Supplier page Find this product

Research areas

Tuberous Sclerosis Complex Research12PI3K/AKT/mTOR signaling in cancer6Polyomavirus and related diseases3Histiocytic Disorders and Treatments3Renal cell carcinoma treatment3Neurofibromatosis and Schwannoma Cases2Heat shock proteins research2Eosinophilic Disorders and Syndromes1

Papers citing this product

1
Functional assessment of variants in the <i>TSC1</i> and <i>TSC2</i> genes identified in individuals with Tuberous Sclerosis Complex
Human Mutation·2011·94 cit.·DOI
2
Tuberous Sclerosis Complex-1 Deficiency Attenuates Diet-Induced Hepatic Lipid Accumulation
PLoS ONE·2011·70 cit.·DOI
3
Inhibition of HSP90 overcomes resistance to chemotherapy and radiotherapy in pancreatic cancer
International Journal of Cancer·2019·64 cit.·DOI
4
Bladder tumour-derived somatic TSC1 missense mutations cause loss of function via distinct mechanisms
Human Molecular Genetics·2008·55 cit.·DOI
5
Cathepsin Protease Controls Copper and Cisplatin Accumulation via Cleavage of the Ctr1 Metal-binding Ectodomain
Journal of Biological Chemistry·2016·54 cit.·DOI
6
Identification of Regions Critical for the Integrity of the TSC1-TSC2-TBC1D7 Complex
PLoS ONE·2014·42 cit.·DOI
7
Identification of a region required for TSC1 stability by functional analysis of TSC1missense mutations found in individuals with tuberous sclerosis complex
BMC Medical Genetics·2009·36 cit.·DOI
8
Missense mutations to the TSC1 gene cause tuberous sclerosis complex
European Journal of Human Genetics·2008·33 cit.·DOI
9
Comparison of the functional and structural characteristics of rare <i>TSC2</i> variants with clinical and genetic findings
Human Mutation·2019·33 cit.·DOI
10
The HSP90 inhibitor onalespib potentiates 177Lu‑DOTATATE therapy in neuroendocrine tumor cells
International Journal of Oncology·2019·30 cit.·DOI

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