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Research 721–750 of 1000+
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Clinical and molecular genetic studies in hereditary hair loss
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families
- Transdifferentiation of corneal epithelium: evidence for a linkage between the segregation of epidermal stem cells and the induction of hair follicles during embryogenesis.
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?
- EDA2R Is Associated with Androgenetic Alopecia
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of β-catenin in mice
- [Androgenetic alopecia].
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Induction of cardiomyocyte‑like cells from hair follicle cells in mice
- Ubiquity and Diversity of Human-Associated Demodex Mites
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Hair curvature: a natural dialectic and review
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- 176 Myeloid cell-specific deletion of mTOR suppresses psoriasis-like skin inflammation in C57BL/6 mice
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene