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Research 121–150 of 1000+
- Two females with hair loss
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Biochemistry of epidermal stem cells
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Optimizing clinical monitoring and management guidelines for capivasertib in HR-positive/HER2-negative advanced breast cancer: expert opinion
- Skin abnormalities generated by temporally controlled RXRα mutations in mouse epidermis
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Alopezien und Hypotrichosen im Kindesalter
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Chapter 23. Therapeutic Control of Androgen Action
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Alopecia: possible causes and treatments, particularly in captive nonhuman primates.
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Influence of NUDT15 Genotyping on Dose Intensity of Thiopurine Administration and Long-Term Clinical Outcomes (Hospitalization and Surgery)
- Spreading of Isolated Ptch Mutant Basal Cell Carcinoma Precursors Is Physiologically Suppressed and Counteracts Tumor Formation in Mice
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Hair for brain trade-off, a metabolic bypass for encephalization