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Research 121–150 of 1000+
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Australasian Society for Dermatology Research Meeting, May 2006
- ANDROGENETIC ALOPECIA
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- The endocrinology of baldness
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Androgen receptor gene polymorphism and biological age markers in men
- Adrenal causes of endocrine hypertension in childhood or adolescence
- UJI EFEKTIVITAS DAN STABILITAS HAIR TONIC EKSTRAK BAWANG MERAH (Allium cepa L.) SEBAGAI PERANGSANG PERTUMBUHAN RAMBUT
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- The molecular pathogenesis of Trichilemmal carcinoma
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- This Month in the Journal
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Predicting Human Appearance from DNA for Forensic Investigations
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction