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Research 391–420 of 1000+
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- The Case | Bilateral kidney tumors and lung cysts
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Southern African HIV Clinicians Society gender-affirming healthcare guideline for South Africa
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- PROTACs: A novel strategy for cancer drug discovery and development
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Developing stratified epithelia: lessons from the epidermis and thymus
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- The Molecular Biology of the Vitamin D Receptor
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- The Role of Probiotics and Synbiotics on Hirsutism
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Genetic Variants and Protective Immunity against SARS-CoV-2
- The emerging roles of N6-methyladenosine (m6A) deregulation in polycystic ovary syndrome
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Hair Pores Caused by Surfactants via the Cell Membrane Complex and a Prevention Strategy through the Use of Cuticle Sealing
- Regulatory mechanisms of LGR4 on cancer and cancer stem cell properties
- Testosterone: The Male Sex Hormone
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Molecular Genetics of Human Hair Diseases
- LB923 A matched cohort study evaluating the risk of keloid development in alopecia areata patients
- Molecular landscape of lung cancer: insights into therapeutic targets and clinical outcomes
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Role of Stearoyl-CoA Desaturase-1 in Skin Integrity and Whole Body Energy Balance