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Publications by L Lipton
Germline Mutations in the TGF-beta and WNT Signalling Pathways Are a Rare Cause of the "Multiple" Adenoma Phenotype
Journal of Medical Genetics
Genetics
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Germline PTEN Mutations Are Rare and Highly Penetrant
Hereditary Cancer in Clinical Practice
Oncology
Genetics
The Lophotrochozoan TGF-β Signalling Cassette - Diversification and Conservation in a Key Signalling Pathway
International Journal of Developmental Biology
Embryology
Developmental Biology
HOXA13 Is a Potential GBM Diagnostic Marker and Promotes Glioma Invasion by Activating the WNT and TGF-β Pathways
Oncotarget
Oncology
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
American Journal of Human Genetics
Genetics
SMARCB1 Mutations Are Not a Common Cause of Multiple Meningiomas
Journal of Medical Genetics
Genetics
Multiple Components of PKA and TGF-β Pathways Are Mutated in Pseudomyxoma Peritonei
PLoS ONE
Multidisciplinary
Germline-Activating RRAS2 Mutations Cause Noonan Syndrome
American Journal of Human Genetics
Genetics
MicroRNA-455 Targets Multiple Genes in the WNT Signalling Pathway
Osteoarthritis and Cartilage
Sports Medicine
Rheumatology
Orthopedics
Biomedical Engineering
A Rare Cause of Hypercalcemia in Childhood; Parathyroid Adenoma: Case Report and Review of the Literature
Guncel Pediatri
Child Health
Pediatrics
Perinatology