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Research 511–540 of 1000+
- Cutaneous and Oral Mucosal Lesions in Cri-du-chat Syndrome
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Female Androgenetic (?) Alopecia
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Functional Enhancers As Master Regulators of Tissue-Specific Gene Regulation and Cancer Development.
- Genetic Hair Disorders: A Review
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Pili annulati with fragility: Electron microscopic findings of a case
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Pathophysiology and Nutritional Approaches in Polycystic Ovary Syndrome (PCOS): A Comprehensive Review
- Zebrafish Model of Hereditary Pigmentary Disorders
- Polycystic ovary syndrome and psychological distress: Urban–rural comparison among reproductive-aged women in Bangladesh
- A missense mutation in Lama3 causes androgen alopecia
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Genome Wide Differential Expression Profiles in Nevus Sebaceous Uncovered Low Expression of CDKN2AIP and Construction of a ceRNA Network
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Society for Endocrinology guidelines for testosterone replacement therapy in male hypogonadism
- Sebaceous Gland Atrophy in Psoriasis: An Explanation for Psoriatic Alopecia?
- Immuno-Endocrinology of COVID-19: The Key Role of Sex Hormones
- Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene
- Types of Human Stem Cells and Their Therapeutic Applications
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Conditional telomerase induction causes proliferation of hair follicle stem cells
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria