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tcf4 protein, human
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Genetic Markers
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Curated Studies
Most Correlated Studies
Colon adenocarcinoma LS174 cells expressing dominant-negative TCF4
Embryonic kidney HEK293 cell transcriptional regulation via Wnt3a with or without SET8 knockdown
Primary acute myeloid leukemia cells treated with IL-3
Mechanism for bone colonization in metastatic lung cancer
Embryonic stem H1 cells with CPRISPR/Cas9-mediated E2A knockout
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Literature
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A typical variant in TCF4 exon 18 is not associated with Pitt-Hopkins syndrome but with a familial c…
Pitt-Hopkins syndrome caused by TCF4 gene novel mutation in a child].
The recurrent TCF4 missense variant p.(Arg389Cys) causes a neurodevelopmental disorder overlapping w…
Learning from osteoporosis: TCF4 as a promising companion biomarker for breast cancer.
Two types of early epileptic encephalopathy in a Pitt-Hopkins syndrome patient with a novel TCF4 mut…
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Safety & Efficacy of AlloRx SCĀ® in PTHS Patients
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