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Research 271–300 of 1000+
- Inhibitory effect of 7DHC and BM15766 in HF organoid culture.
- A multi-omic single-cell landscape of perinatal mouse skin maps lineage specification and reveals shared dynamics in human fetal skin
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Trichothiodystrophy hair shafts display distinct ultrastructural features
- Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle
- Sustainability of functional hair follicle activity: Impact of spatially anchored multifunctional tetrahedral framework nucleic acids
- Influence of Scalp Problems on Physical Properties of Hair and Their Prevention by Plant Extracts
- Characterization of Growth Secondary Hair in Min Pig Activated by Follicle Stem Cell Stimulated by Wnt and BMP Signaling Pathway
- Establishment of a culture model for the prolonged maintenance of chicken feather follicles structure in vitro
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Hypomyelinating leukodystrophy-10 presenting with an additional atypical feature of increased body hair and Mongolian spots
- 600 Differential Molecular Signature of Dermal Papilla Cells (DPCs) from Balding and Non balding Scalp in 2D, 3D culture and Co-culture with Adipose-derived stem cells (ASCs)
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Runx3 is involved in hair shape determination
- Epigen Transgenic Mice Develop Enlarged Sebaceous Glands
- Isolation and Characterization of Mouse High-glycine/Tyrosine Proteins
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- μ-Crystallin, Thyroid Hormone-binding Protein, is Expressed Abundantly in the Murine Inner Root Sheath Cells
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- 14-3-3σ Is Required for Club Hair Retention
- Wnt-10b promotes differentiation of skin epithelial cells in vitro
- Copy number variation regions in Nellore cattle: Evidences of environment adaptation
- 186 Dissecting the role of the common neurotrophin receptor CD271 in the skin: generation and characterization of a novel mouse model with keratinocyte-specific conditional deletion
- Anatomy and Physiology of Hair
- The biology and genetics of curly hair
- Advances in Hair Diseases