October 15, 1998Open Access

FGFR3 Gene Mutations Associated With Human Skeletal Disorders Occur Rarely in Multiple Myeloma

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Abstract

FGFR3 gene mutations associated with human skeletal disorders occur rarely in multiple myeloma. N. S. Fracchiolla; LUMINARI, Stefano ; L. Baldini; L. Lombardi; A. T. Maiolo; A. Neri 1998 Abstract no abstract available

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Fracchiolla et al. (Thu,) studied this question.

synapsesocial.com/papers/6a1fc1bac9d0b876165fcab5 https://doi.org/https://doi.org/10.1182/blood.v92.8.2987

Also Consider

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1Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 31997 · 647 citations
2Constitutive activation of fibroblast growth factor receptor 3 by mutations responsible for the lethal skeletal dysplasia thanatophoric dysplasia type I.1998 · 75 citations
3Basic fibroblast growth factor and hematopoiesis.1995 · 62 citations
4Isolation of an additional member of the fibroblast growth factor receptor family, FGFR-3.1991 · 414 citations
5'Role of bone marrow stromal cells in the growth of human multiple myeloma1991 · 196 citations

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