Search
for
Sort by
Research 151–180 of 1000+
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Contents
- Tissue Expansion and Serial Excision in Scar Revision
- Primary Hypothyroidism and Thyroid Goiter in an Adult Cat
- The Role of Histone Demethylases in Disease
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- Breast Embryology, Anatomy, and Physiology
- Ear pinna growth and differentiation is conserved in murids and requires BMP signaling for chondrocyte proliferation
- Update on hidradenitis suppurativa: connecting the tracts
- Stem Cells Applications in Regenerative Medicine and Disease Therapeutics
- Research Relevant Conditions and Pathology in Nonhuman Primates
- EFFECTS of SOME CHEMICALS in COSMETIC PRODUCTS on PREGNANT, FETUS and NEWBORN HEALTH
- 864 Catalytic-dependent and -independent activities of Polycomb repressive complex 1 differentially regulate skin stem cell specification
- Congenital hair loss disorders: Rare, but not too rare
- The effect of experimental hypothyroidism on the skin of adult male albino rats and the therapeutic role of topical triiodothyronine
- Skin Manifestations in Primary Immunodeficient Children
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Congenital adrenal hyperplasia
- Congenital atrichia and hypotrichosis
- A Case of Basal Cell Carcinoma Arising in Congenital Triangular Alopecia
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Melanocyte stem cells: a melanocyte reservoir in hair follicles for hair and skin pigmentation
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital hypotrichosis due to short anagen
- Congenital Atrichia: A Case Report