Laron Syndrome Research Paves the Way for New Insights in Oncological Investigation.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
09 11 2020
Historique:
received: 18 10 2020
revised: 04 11 2020
accepted: 05 11 2020
entrez: 13 11 2020
pubmed: 14 11 2020
medline: 17 6 2021
Statut: epublish

Résumé

Laron syndrome (LS) is a rare genetic endocrinopathy that results from mutation of the growth hormone receptor (

Identifiants

pubmed: 33182502
pii: cells9112446
doi: 10.3390/cells9112446
pmc: PMC7696416
pii:
doi:

Substances chimiques

Intercellular Signaling Peptides and Proteins 0
Insulin-Like Growth Factor I 67763-96-6

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Haim Werner (H)

Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.
Shalom and Varda Yoran Institute for Human Genome Research, Tel Aviv University, Tel Aviv 69978, Israel.

Rive Sarfstein (R)

Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.

Karthik Nagaraj (K)

Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.

Zvi Laron (Z)

Endocrine and Diabetes Research Unit, Schneider Children's Medical Center, Petah Tikva 49292, Israel.

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Classifications MeSH