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Research 91–120 of 1000+
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Case Study: Hereditary Cancer Genetic Testing in Unaffected Patients May Allow for Early Intervention and Aggressive Management
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Clinical and molecular genetic studies in hereditary hair loss
- IMMUNOLOGICAL AND GENETIC ASPECTS OF HEREDITARY ANTIBODY DEFICIENCIES
- Testosterone stimulates proliferation and inhibits interleukin‐6 production of normal and hereditary gingival fibromatosis fibroblasts
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Multiple, hereditary dome-shaped papules and acrochordons. Birt-Hogg-Dube syndrome
- Editorial: Vitamin D 1α-Hydroxylase Knockout Mice as a Hereditary Rickets Animal Model
- Real-World Outcomes and Healthcare Utilization of Lanadelumab in Spain: Insights from First Cohort of Difficult-to-Treat Hereditary Angioedema Cases
- Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Hair Loss, Insulin Resistance, and Heredity in Middle-aged Women. a Population-based Study
- The human keratins: biology and pathology
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Keratins of the Human Hair Follicle
- Genetic Basis of Male Pattern Baldness
- Genetic Disorders and Defects in Vitamin D Action
- Hair follicle group and skin follicle population of Australian Merino sheep
- The role of vitamin D receptor mutations in the development of alopecia
- ANALYSIS OF THE RELATION BETWEEN ALOPECIA AND RESISTANCE TO 1,25‐DIHYDROXYVITAMIN D
- Reversal of Baldness in Patient Receiving Minoxidil for Hypertension
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Central hair loss in African American women: Incidence and potential risk factors