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Research 31–60 of 1000+
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Filaggrin mutations as an archetype for understanding the pathophysiology of atopic dermatitis
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Selective Expression of Calcium-Binding Proteins S100A8 and S100A9 at Distinct Sites of Hair Follicles
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Importance of Citrullination on Hair Protein Molecular Assembly During Trichocytic Differentiation
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- Identification of Trichohyalin-Like 1, an S100 Fused-Type Protein Selectively Expressed in Hair Follicles
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Ultrastructural Localization of S100A3, a Cysteine-rich, Calcium Binding Protein, in Human Scalp Hair Shafts Revealed by Rapid-freezing Immunocytochemistry
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Microarray analysis of androgenetic and senescent alopecia: Comparison of gene expression shows two distinct profiles
- Palatogenesis and cutaneous repair: A two‐headed coin
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Specific Citrullination Causes Assembly of a Globular S100A3 Homotetramer
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- iε-(γ<sup>-Glutamyl</sup>) lysine cross-linkage in citrulline-containing protein fractions from hair
- Human Trichohyalin Gene Is Clustered with the Genes for Other Epidermal Structural Proteins and Calcium-Binding Proteins at Chromosomal Locus 1q21
- A group of type I keratin genes on human chromosome 17: characterization and expression.
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Do Changes in Chromosomes Cause Aging?
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family