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Research 631–660 of 1000+
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Moniletherix
- SEXUAL DIMORPHISM IN MAMMALS
- Tissue engineering strategies combining molecular targets against inflammation and fibrosis, and umbilical cord blood stem cells to improve hampered muscle and skin regeneration following cleft repair
- Hair trace elementary profiles in aging rodents and primates: links to altered cell homeodynamics and disease
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Meibomian gland changes in the rhino (hrrhhrrh) mouse.
- Physiological Insights from the Vitamin D Receptor Knockout Mouse
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Clinical Study to Evaluate the Efficacy and Safety of a Hair Serum Product in Healthy Adult Male and Female Volunteers with Hair Fall
- Monilethrix: A rare hereditary condition
- The profile of steroid hormones in human fetal and adult ovaries
- Advances in the treatment of male androgenetic alopecia: a brief review of finasteride studies.
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Giant congenital cerebriform pigmented nevus of scalp: case report
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Zinc-responsive Acral Hyperkeratosis as a Sequele of Acrodermatitis Enteropathica
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Skin and Menopause
- Alopecia Universalis with Frequently Relapsing Nephrotic Syndrome of Infantile Onset: A Rare Presentation
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome