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Research 61–90 of 1000+
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- 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
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Generation of Genetically Modified Rats Using CRISPR/Cas9 Genome-Editing System to Reveal Novel Vitamin D Actions
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- Prevalence and Etiology of Central Centrifugal Cicatricial Alopecia
- Protective cardiovascular and renal actions of vitamin D and estrogen
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Recomendations on non-pharmacological interventions in women with PCOS to reduce body weight and improve metabolic disorders [Zalecenia dotyczące postępowania niefarmakologicznego u kobiet z PCOS celem zmniejszenia masy ciała i poprawy zaburzeń metabolicznych]
- Role of the vitamin D receptor in hair follicle biology
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Extraskeletal actions of vitamin D
- 1,25-dihydroxyvitamin D resistance, rickets, and alopecia
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- Effect of a transcriptional inactive or absent vitamin D receptor on beta-cell function and glucose homeostasis in mice
- Functional analysis of vitamin D receptor (VDR) using adenovirus vector
- Vitamin D and skin diseases: A review
- The role of vitamin D receptor mutations in the development of alopecia
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- VDR is an essential regulator of hair follicle regression through the progression of cell death
- Lymphoid Enhancer-binding Factor-1 (LEF1) Interacts with the DNA-binding Domain of the Vitamin D Receptor
- Study of vitamin D deficiency in patients with alopecia areata attending a dermatology center in Iran
- Studying the relationship betweenSerum Copper levels and Vitamin D in Alopecia Areata patients with Controls in India
- Prevalence of Cobalt in the Environment and Its Role in Biological Processes
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Vitamin D: A Bridging Element for Wellness; A Case Study on Vitamin D Deficiency and its Association with Alopecia Areata and Other Conditions
- Association of vitamin D level with alopecia areata