Reactome: A Curated Pathway Database
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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person Refetoff, Samuel

Class:IdPerson:5658168
_displayNameRefetoff, Samuel
_timestamp2014-12-18 12:08:30
created[InstanceEdit:5658180] Jassal, Bijay, 2014-12-18
firstnameSamuel
initialS
surnameRefetoff
(author)[LiteratureReference:5658190] Genetic causes of congenital hypothyroidism due to dyshormonogenesis
[LiteratureReference:9961641] Identification of the maturation factor for dual oxidase. Evolution of an eukaryotic operon equivalent
[LiteratureReference:9961668] Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism
[LiteratureReference:9962025] Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone Metabolism
[LiteratureReference:9962409] GLIS3 is indispensable for TSH/TSHR-dependent thyroid hormone biosynthesis and follicular cell proliferation
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No pathways have been reviewed or authored by Refetoff, Samuel (5658168)