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neurofibromatosis I
Summary
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Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
Plexiform neurofibroma NF1-deficient ipNF05.5 and ipNF9511.bc cells resistant to TAK-733
Dermal fibroblasts from neurofibroma surrounding tissue with SVEP1 siRNA knockdown
Schwannoma and grade I meningioma's gene expression profiles
Malignant peripheral nerve sheath tumor orthoxenograft models
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Literature
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Destabilizing NF1 variants act in a dominant negative manner through neurofibromin dimerization.
The therapeutic potential of neurofibromin signaling pathways and binding partners.
New insights into the molecular basis of spinal neurofibromatosis type 1.
Neurofibromatosis type 1 families with first-degree relatives harbouring distinct NF1 pathogenic var…
Analysis of 200 unrelated individuals with a constitutional NF1 deep intronic pathogenic variant rev…
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A Long-term Study of NPC-12G Gel in Neurofibromatosis Type I
A Clinical Trial to Evaluate the Tolerability and Pharmacokinetics of TQ-B3234 in Patients With Type…
Topical Rapamycin Therapy to Alleviate Cutaneous Manifestations of Tuberous Sclerosis Complex (TSC) …
Trial to Evaluate the Safety of Lovastatin in Individuals With Neurofibromatosis Type I (NF1)
Pirfenidone in Children and Young Adults With Neurofibromatosis Type I and Progressive Plexiform Neu…
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