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Research 241–270 of 1000+
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Depletion of S100A4+ stromal cells results in abnormal nipple development and nursing failure
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study
- Disease causing homozygous variants in the human hairless gene
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Androgen receptor gene CAG and GGN polymorphisms in infertile Nigerian men
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- Keratin disorders: from gene to therapy
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- The promoter of an androgen dependent gene in the hamster flank organ
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Performance exploration of multi-gene panels of alopecia areata susceptibility and drug-binding targets
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Structure of human type II 5 alpha-reductase gene.
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Cloning, computational analysis and expression profiling of steroid 5 alpha-reductase 1 (SRD5A1) gene during reproductive phases and ovatide stimulation in endangered catfish, Clarias magur
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Combined Deletion of the Vitamin D Receptor and Calcium-Sensing Receptor Delays Wound Re-epithelialization
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Hair, Cutaneous Homeostasis and Stem Cell Functions
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Molecular basis of hypohidrotic ectodermal dysplasia: an update