Concepedia

Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

Nelly Pitteloud, Astrid U. Meysing, Richard Quinton, James S. Acierno, Andrew Dwyer, Lacey Plummer, Eric Fliers, Paul A. Boepple, Frances J. Hayes, Stephanie B. Seminara,

Molecular and Cellular Endocrinology · 2006 · 198 citations · 33 references

Concepts

Life SciencesGeneticsMolecular GeneticsCell SignalingHuman GeneticsInfertilityCongenital Endocrine DisordersCongenital MalformationsCongenital Reproductive AnomaliesGenetic DisordersGrowth Factor SignalingFibroblast AbnormalitiesFibroblast Growth Factor Receptor AlterationsFibroblast Growth Factor Receptor SignalingMutations In Fibroblast Growth Factor Signaling Pathway

References

33

Molecular and Cellular Endocrinology

William E. Rainey, Raymond J. Rodgers · Molecular and Cellular Endocrinology · 2004 · 1.3K citations

Life Sciences, Cell Biology, Endocrinology +12

Crystal Structure of a Ternary FGF-FGFR-Heparin Complex Reveals a Dual Role for Heparin in FGFR Binding and Dimerization

Joseph Schlessinger, A.N. Plotnikov, Omar A. Ibrahimi et al. · Molecular Cell · 2000 · 1.2K citations · Full text

Life Sciences, Biochemistry, Molecular Biology +15

Origin of luteinizing hormone-releasing hormone neurons

Marlene Schwanzel‐Fukuda, Donald W. Pfaff · Nature · 1989 · 1.1K citations

Life Sciences, Neurobiology, Neuroscience +10

Recommendations for a nomenclature system for human gene mutations

Stylianos E. Antonarakis · Human Mutation · 1998 · 939 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Brunella Franco, Silvana Guioli, Antonella Pragliola et al. · Nature · 1991 · 851 citations

Life Sciences, Genetics, Molecular Genetics +13