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Research 91–120 of 1000+
- Regulation of a hair follicle keratin intermediate filament gene promoter
- Hypotrichosis and Hair Loss on the Occipital Scalp
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population
- The ITGB6 gene: its role in experimental and clinical biology
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- [Peptidergic innervation in the sinus hair follicles of several mammalian species].
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- A Comparative study of Regulations of Cell and Gene therapy in US, EU and India
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Basonuclin is associated with the ribosomal RNA genes on human keratinocyte mitotic chromosomes
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Expression of the Intermediate Filament Keratin Gene,K15,in the Basal Cell Layers of Epithelia and the Hair Follicle
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Atrichia with papular lesions resulting from a novel homozygous missense mutation in the hairless gene
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Pilomatricoma in the infraorbital region
- Regulation of Involucrin Gene Expression
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Cloning and sequence analysis of KAP 6.1 gene in Xinjiang fine-wool sheep
- The Agouti Gene in Obesity: Central and Peripheral Mechanisms, and Therapeutic Implications
- HOXC13 Is Involved in the Regulation of Human Hair Keratin Gene Expression