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Research 30 of 220
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- What does acne genetics teach us about disease pathogenesis?
- Genetic Defects of Female Sexual Differentiation
- Food and medicine homology: a potential nutritional intervention strategy for post-acute COVID-19 syndrome
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Biology and Genetics of Hair
- Ptosis in childhood
- Tissue-Specific Multi-Omics Integration Demonstrates Molecular Signatures Connecting Obesity to Immune Vulnerability
- Discovery of genes and proteins possibly regulating mean wool fibre diameter using cDNA microarray and proteomic approaches
- Regulation of masculinization: androgen signalling for external genitalia development
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- Aligning Stem Cell Models and Postmortem Studies to Query Striatal Neurodevelopment in Schizophrenia
- Wounds and the Microbiota: The Healing Interplay Between Host and Microbial Communities
- Green Nanodrugs: Research Progress and Challenges of Plant-Derived Nanovesicles in Tumor Treatment
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- FOXN1 deficient nude severe combined immunodeficiency
- The Potential of Hair Matrix for Biomarker Analysis in Schizophrenia
- Mendelian randomization analysis of the causal relationship between low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and androgenic alopecia
- Male infertility and genitourinary birth defects: there is more than meets the eye