Associated Papers
Rare Homozygous Variants in INSR and NFXL1 Are Associated with Severe Treatment-Resistant Psychosis.
Kanwal A et al.
International Journal of Molecular Sciences, 2025
40430072 (PubMed )
Supplement: ijms-26-04925-s001.zip › ijms-3618587-supplementary.pdf
Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan.
Hassan SS et al.
Pediatric Diabetes, 2024
INS-gene mutations: from genetics and beta cell biology to clinical disease.
Liu M et al.
Molecular Aspects of Medicine, 2015
Binding specificity and mutational analysis of the phosphotyrosine binding domain of the brain-specific adaptor protein ShcC.
O'Bryan JP et al.
The Journal of Biological Chemistry, 1996
[Recombinant DNA in the study of diabetes mellitus].
Pankov IuA
Molekuliarnaia Biologiia, 0
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