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Research 691–720 of 1000+
- Exploiting molecular genetic diagnoses of polycystic ovary syndrome to achieve better patient outcome
- Clinical Snippets
- 918 Tissue engineered human hair follicles from genetically, environmentally and extrinsically reprogrammed dermal papilla cells
- 성장기 모낭에서 큐티클층의 각질화 과정
- The role of functional variants in the aetiology of polycystic ovary syndrome
- Few Simple Sequence Repeats in Human Hair
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- Ultrastructural Characteristics of Neonate Scalp Hair
- Abstract 4385: Live-imaging the interface between homeostasis and cancer initiation
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Healthy Hair: Form and Function
- The acne hormones
- Alopecias
- Phenobarbital
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- A mouse with bad hair and poor taste
- اثر تستوسترون اگزوژن و داروی Finasteride بر بی دردی ناشی از مورفین در موش های سوری نر با استفاده از تست فرمالین
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Cloning and Activity of Mouse Ultra-High Sulfur Keratin Gene Promoter
- Hair Sciences: The hair cycle discussed with Dr. Gilliam Westgate
- Morphologic comparison of cultured human epidermis melanocytes,amelanotic melanocytes from hair follicles and mouse melanoma cells observed by atomic force microscope
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- A Case of pretibial myxedema with hyperthyroidism
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Geographical Differences in Male Infertility between the United States and Canada: Insights from the Andrology Research Consortium
- Cells and Structures Involved in Hair Follicle Regeneration: An Introduction
- Characteristics of finasteride users in comparison with nonusers: A Nordic nationwide study based on individual‐level data from Denmark, Finland, and Sweden
- Early-onset androgenetic alopecia and endocrine disruptors
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex