Search
for
Sort by
Research 31–60 of 1000+
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Multi-omics and AI-driven advances in miRNA-mediated hair follicle regulation in cashmere goats
- Polycystic ovarian syndrome: Prevalence and its correlates among adolescent girls
- Prevalence of signs and symptoms among iron deficient college-age individuals and its use as a predictor of iron deficiency
- Connexin mutations in human disease
- Non-Hormonal Treatment Options for Regulation of Menstrual Cycle in Adolescents with PCOS
- PCOS – The Importance of Diet, Physical Activity, and Other Non-Pharmacological Methods in Treatment
- Metabolomic biomarkers in women with polycystic ovary syndrome: a pilot study
- Telogen hair loss and androgenetic‐like alopecia in GAPO syndrome
- Comparison of prevalence of periodontal disease in women with polycystic ovary syndrome and healthy controls
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- The Effects of FemmeBalance Supplement on Symptoms of Premenstrual Syndrome: A Four-Cycle Single-Arm Observational Study of a Novel Nutritional Supplement
- Somatization in the dermatology patient: Some sociocultural perspectives
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- [Regression analysis of serum bone metabolic markers and traditional Chinese medicine syndromes in patients with CKD-MBD].
- Hair Evaluation in Orthodontic Patients with Oligodontia
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Hair shaft disorders in children – An update
- Can UK undergraduate dental programmes provide training in non-surgical facial aesthetics?
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- How to diagnose a lipodystrophy syndrome
- Non-apoptotic role for caspase-7 in hair follicles and the surrounding tissue
- Syndromes of Severe Insulin Resistance (SSIRs)
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome