Qin W, Liu Z, Huang M, Liang L, Gan Y, Huang Z
Int J Mol Sci. 2025; 26(4).
PMID: 40003893
PMC: 11855556.
DOI: 10.3390/ijms26041425.
Xu L, Jang H, Nussinov R
Protein Sci. 2025; 34(2):e70042.
PMID: 39840811
PMC: 11751910.
DOI: 10.1002/pro.70042.
Nussinov R, Jang H, Cheng F
Neurochem Int. 2024; 181:105883.
PMID: 39427854
PMC: 11614691.
DOI: 10.1016/j.neuint.2024.105883.
Healy F, Turner A, Marensi V, MacEwan D
Front Pharmacol. 2024; 15:1441938.
PMID: 39372214
PMC: 11450236.
DOI: 10.3389/fphar.2024.1441938.
Ferrito N, Baez-Flores J, Rodriguez-Martin M, Sastre-Rodriguez J, Coppola A, Isidoro-Garcia M
Int J Mol Sci. 2024; 25(16).
PMID: 39201250
PMC: 11354534.
DOI: 10.3390/ijms25168563.
RASopathies - what they reveal about RAS/MAPK signaling in skeletal muscle development.
Rauen K, Tidyman W
Dis Model Mech. 2024; 17(6).
PMID: 38847227
PMC: 11179721.
DOI: 10.1242/dmm.050609.
RASopathies: Evolving Concepts in Pathogenetics, Clinical Features, and Management.
Padhiyar J, Mahajan R, Panda M
Indian Dermatol Online J. 2024; 15(3):392-404.
PMID: 38845651
PMC: 11152490.
DOI: 10.4103/idoj.idoj_594_23.
Hyperactivation of MEK1 in cortical glutamatergic neurons results in projection axon deficits and aberrant motor learning.
Bjorklund G, Rees K, Balasubramanian K, Hewitt L, Nishimura K, Newbern J
Dis Model Mech. 2024; 17(6).
PMID: 38826084
PMC: 11247507.
DOI: 10.1242/dmm.050570.
Paternally Inherited Noonan Syndrome Caused by a Variant May Exhibit Mild Symptoms: A Case Report and Literature Review.
Han J, Park J
Genes (Basel). 2024; 15(4).
PMID: 38674380
PMC: 11050143.
DOI: 10.3390/genes15040445.
Autism spectrum disorder profiles in RASopathies: A systematic review.
Debbaut E, Steyaert J, El Bakkali M
Mol Genet Genomic Med. 2024; 12(4):e2428.
PMID: 38581124
PMC: 10997847.
DOI: 10.1002/mgg3.2428.
Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart.
Waheed-Ullah Q, Wilsdon A, Abbad A, Rochette S, BuLock F, Hitz M
J Anat. 2024; 245(1):70-83.
PMID: 38419169
PMC: 11161829.
DOI: 10.1111/joa.14033.
Reporter cell lines to screen for inhibitors or regulators of the KRAS-RAF-MEK1/2-ERK1/2 pathway.
Weatherdon L, Stuart K, Cassidy M, de la Gandara A, Okkenhaug H, Muellener M
Biochem J. 2024; 481(6):405-422.
PMID: 38381045
PMC: 11088904.
DOI: 10.1042/BCJ20240015.
Expanding the Genetic Code of Embryos.
Brown W, Davidson L, Deiters A
ACS Chem Biol. 2024; 19(2):516-525.
PMID: 38277773
PMC: 10877573.
DOI: 10.1021/acschembio.3c00686.
Time-dependent effects of BRAF-V600E on cell cycling, metabolism, and function in engineered myocardium.
Strash N, DeLuca S, Janer Carattini G, Chen Y, Wu T, Helfer A
Sci Adv. 2024; 10(4):eadh2598.
PMID: 38266090
PMC: 10807800.
DOI: 10.1126/sciadv.adh2598.
Epilepsy in cardiofaciocutaneous syndrome: Clinical burden and response to anti-seizure medication.
Kenney-Jung D, Collazo-Lopez J, Rogers D, Shanley R, Zatkalik A, Whitmarsh A
Am J Med Genet A. 2023; 194(2):301-310.
PMID: 37827855
PMC: 10843452.
DOI: 10.1002/ajmg.a.63428.
Genetically Encoded Aminocoumarin Lysine for Optical Control of Protein-Nucleotide Interactions in Zebrafish Embryos.
Brown W, Wesalo J, Samanta S, Luo J, Caldwell S, Tsang M
ACS Chem Biol. 2023; 18(6):1305-1314.
PMID: 37272594
PMC: 10278064.
DOI: 10.1021/acschembio.3c00028.
Prenatal Diagnosis of Euploid Increased Nuchal Translucency on Fetal Ultrasound (II): RASopathy Disorders - Prenatal Ultrasound Findings and Genotype-phenotype Correlations.
Chen C
J Med Ultrasound. 2023; 31(1):13-16.
PMID: 37180632
PMC: 10173828.
DOI: 10.4103/jmu.jmu_79_22.
A dimensional approach to neurodevelopmental differences in genetically well-defined populations: What's next?.
Pierpont E
Dev Med Child Neurol. 2023; 65(11):1420-1421.
PMID: 37130209
PMC: 11044890.
DOI: 10.1111/dmcn.15634.
The therapeutic potential of neurofibromin signaling pathways and binding partners.
Baez-Flores J, Rodriguez-Martin M, Lacal J
Commun Biol. 2023; 6(1):436.
PMID: 37081086
PMC: 10119308.
DOI: 10.1038/s42003-023-04815-0.
Prenatal Clinical Findings in -Related Capillary Malformation-Arteriovenous Malformation Syndrome.
Coccia E, Valeri L, Zuntini R, Caraffi S, Peluso F, Pagliai L
Genes (Basel). 2023; 14(3).
PMID: 36980822
PMC: 10048332.
DOI: 10.3390/genes14030549.