Search
for
Sort by
Research 841–870 of 1000+
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Keratinocyte growth factor is an important endogenous mediator of hair follicle growth, development, and differentiation. Normalization of the nu/nu follicular differentiation defect and amelioration of chemotherapy-induced alopecia.
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Frizzled Receptors in Development and Disease
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Therapeutic anti-inflammatory potential of formyl-peptide receptor agonists
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Regulation of Keratin Gene Expression in Hair Follicle Differentiation<sup>a</sup>
- Male pseudohermaphroditism due to 17β-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Keratinization and its Disorders
- Human hair keratins
- THE PATHOGENESIS OF ALOPECIA AREATA
- Molecular Regulation of Melanocyte Senescence
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Androgenetic alopecia in children: report of 20 cases
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13