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- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Congenital Atrichia: A Case Report
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- A Newborn With Hair Loss
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Alopecia: Association with Resistance to Thyroid Hormones
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Two females with hair loss
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Testing Chemotherapeutic Agents in the Feather Follicle Identifies a Selective Blockade of Cell Proliferation and a Key Role for Sonic Hedgehog Signaling in Chemotherapy-Induced Tissue Damage
- Induction of hair follicle dermal papilla cell properties in human induced pluripotent stem cell-derived multipotent LNGFR(+)THY-1(+) mesenchymal cells
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Visualising Androgen Receptor Activity in Male and Female Mice
- Botryococcus terribilis Ethanol Extract Exerts Anti-inflammatory Effects on Murine RAW264 Cells
- Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments.
- Biomedical applications of organoids in genetic diseases
- E-Poster
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation