| human | Q5 |
| P6178 | Dimensions author ID | 0726656367.17 |
| P496 | ORCID iD | 0000-0002-0978-5401 |
| P734 | family name | Peskett | Q96478400 |
| P735 | given name | Emma | Q541194 |
| Emma | Q541194 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q37644520 | Analysis of the Fgfr2C342Y mouse model shows condensation defects due to misregulation of Sox9 expression in prechondrocytic mesenchyme |
| Q64928872 | Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages. |
| Q28594707 | Critical role for the p110alpha phosphoinositide-3-OH kinase in growth and metabolic regulation |
| Q98463838 | Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations |
| Q28288981 | Essential role for the p110delta phosphoinositide 3-kinase in the allergic response |
| Q50000808 | Genetic Analyses in Small for Gestational Age Newborns. |
| Q39650635 | Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants |
| Q28215433 | Impaired B and T cell antigen receptor signaling in p110delta PI 3-kinase mutant mice |
| Q24321833 | Impaired neutrophil migration and phagocytosis in IRAK-4 deficiency |
| Q50983672 | Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortion |
| Q35628225 | Mechanical properties of calvarial bones in a mouse model for craniosynostosis |
| Q24306468 | Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations |
| Q54989348 | Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. |
| Q59793278 | Overexpression of causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouse |
| Q52690998 | SNX14 mutations affect endoplasmic reticulum associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20. |
| Q47396418 | X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations. |
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