Associated Papers
Understanding pain perception through genetic painlessness diseases: The role of NGF and proNGF.
Testa G et al.
Pharmacological Research, 2021
NOTCH and DNA repair pathways are more frequently targeted by genomic alterations in inflammatory than in non-inflammatory breast cancers.
Bertucci F et al.
Molecular Oncology, 2020
31854063 (PubMed )
Supplement: MOL2-14-504-s010.xlsx › TableS3
Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.
Al-Mubarak B et al.
Scientific Reports, 2017
Missense mutations in the NDP gene in patients with a less severe course of Norrie disease.
Meindl A et al.
Human Molecular Genetics, 1995
A third HSAN5 mutation disrupts the nerve growth factor furin cleavage site.
Shaikh SS et al.
Molecular Pain, 0
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