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Research 241–270 of 1000+
- Metabolic Engineering of Microorganisms to Produce L-Aspartate and Its Derivatives
- Alopecia in women submitted to childhood X-ray epilation for tinea capitis treatment
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Mucocutaneous Manifestations of Endocrine Disorders
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Melanocytes and Vitiligo (and Hair Graying)
- Replicative stress, stem cells and aging
- Oncogenic senescence: a multi-functional perspective
- Molecular pathology of skin adnexal tumours
- Nonclassic Congenital Adrenal Hyperplasia
- Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- Epidermal growth factor, innovation and safety
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- The crosstalk of monocyte-neutrophil in hair follicles regulates neutrophil transepidermal migration in contact dermatitis
- Dermatoscopy of hair shaft disorders
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Helpful diagnostic markers of steroidogenesis for defining hyperandrogenemia in hirsute women
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Stem Cells and their Niches
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- 公表学術論文等リスト 2018
- Genetic Fate Mapping Using Site-Specific Recombinases
- Male fertility and skin diseases
- Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities