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Research 751–780 of 1000+
- Decreased Serum Ferritin is Associated With Alopecia in Women
- Epidemiology and burden of alopecia areata: a systematic review
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Animal Models and the Developmental Origins of Polycystic Ovary Syndrome: Increasing Evidence for the Role of Androgens in Programming Reproductive and Metabolic Dysfunction
- Central centrifugal cicatricial alopecia: challenges and solutions
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Identification of SNPs and expression patterns of FZD3 gene and its effect on wool traits in Chinese Merino sheep (Xinjiang Type)
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Azathioprine-induced Agranulocytosis and Severe Alopecia After Kidney Transplantation Associated With a NUDT15 Polymorphism: A Case Report
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Coexistence of psoriasis, and alopecia areata with trachyonychia in a pediatric patient with Turner Syndrome
- A Case of Steatocystoma Multiplex in a Psoriatic Patient during Treatment with Anti-IL-12/23
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Mechanisms of aluminium toxicity, tolerance and amelioration in wheat
- Zebrafish Model of Hereditary Pigmentary Disorders
- Framing the Problem: The Mystery of Post-Finasteride Syndrome and Reasons to Suspect a Microbial Factor
- Unraveling the Molecular Mechanism of Bider Marking Formation in Dun Mongolian Horses Through Transcriptome Sequencing
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Gray Hair: From Preventive to Treatment
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Faculty Opinions recommendation of Hidradenitis suppurativa as a potential subtype of autoinflammatory keratinization disease.
- KRT16 wt Allele
- 線維芽細胞凝集塊形成による幹細胞形成機構の解明
- Hair loss in children.
- Melasma and Endocrine Disorders