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- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Exploring Human Skin Aging at the Single-Cell Level
- The Role of Nrf2 in Hearing Loss
- Transcriptional signatures of secondary hair follicles during annual cashmere growth
- Transcriptional Profiling in Rat Hair Follicles following Simulated Blast Insult: A New Diagnostic Tool for Traumatic Brain Injury
- Skin expression of mammalian target of rapamycin and forkhead box transcription factor O1, and serum insulin‐like growth factor‐1 in patients with acne vulgaris and their relationship with diet
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- SARS-CoV-2 infection reduces the number of spermatogonial stem cells and dysregulates the transcriptional landscape of the human testis
- Stem Cell-Based Hair Cell Regeneration and Therapy in the Inner Ear
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- Delayed granulomatous eruption of the nose associated with ruxolitinib
- Deciphering the Mesodermal Potency of Porcine Skin-Derived Progenitors (SKP) by Microarray Analysis
- The Paradox of p53: What, How, and Why?
- Defining the identity of mouse embryonic dermal fibroblasts
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Oestrogen functions in skin and skin appendages
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- Le gène<i>hairless</i>de la souris
- Multi-scale spatial mapping of cell populations across anatomical sites in healthy human skin and basal cell carcinoma
- Molecular genetics of androgen insensitivity
- XIAP Stabilizes DDRGK1 to Promote ER‐Phagy and Protects Against Noise‐Induced Hearing Loss
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Melanocytes and Vitiligo (and Hair Graying)
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis