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Research 121–150 of 1000+
- Diseases of the Hair
- Hair Shaft Disorders
- Structure and expression of genes for a class of cysteine-rich proteins of the cuticle layers of differentiating wool and hair follicles.
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- THE PEDIATRICIAN AND THE SEXUALLY ACTIVE ADOLESCENT
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- 175 Reinventing the Selfie: Telemedicine in a Tertiary Referral Sexual Medicine Practice
- 繰返し水平荷重を受ける筋違付鉄骨ラーメンの弾塑性性状に関する研究 : (その5)-歪硬化モデルを用いた理論解析-I- : 構造
- The keratins and their disorders
- Message of nexin 1, a serine protease inhibitor, is accumulated in the follicular papilla during anagen of the hair cycle
- Structure and site of expression of a murine type II hair keratin
- Methodology and Challenges to Recruitment to a Randomized, Double-Blind, Placebo-Controlled Trial of Oral DHEA in Postmenopausal Women
- Comparison between dutasteride and finasteride in hair regrowth and reversal of miniaturization in male and female androgenetic alopecia: a systematic review
- 056 IKZF1 and IKAROS overexpression contributes to the pathogenesis of alopecia areata
- Contents
- Genes for intermediate filament proteins and the draft sequence of the human genome
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Itpr3 Is Responsible for the Mouse Tufted (tf) Locus
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- ダブルストロボレンジファインダの開発(特別講演)(画像センシングおよび一般)
- A kindred with mutant IKAROS and autoimmunity
- Formation and Structure: An Introduction to Hair
- OXI1 kinase is necessary for oxidative burst-mediated signalling in Arabidopsis
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- JAK inhibitors for alopecia areata: a systematic review and meta‐analysis
- The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- IDIOPATHIC HYPOPARATHYROIDISM; A REPORT OF 2 CASES