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- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Hair root studies in patients suffering from primary and secondary syphilis
- HAIR-ROOT ADAPTATION TO MARASMUS IN ANDEAN INDIAN CHILDREN
- EFFECT OF POTASSIUM ON BLOOD-SUGAR AND PLASMA-INSULIN LEVELS IN PATIENTS UNDERGOING PERITONEAL DIALYSIS AND HÆMODIALYSIS
- [Changes in telogen rate, hair density, hair diameter and rate of growth in androgenetic alopecia of the male. Simultaneously a contribution to the significance of dysplastic hair].
- Histological and dermatoscopic description of sphynx cat skin
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- 571 Role of observation for excisionally biopsied moderately dysplastic nevi with positive histologic margins and risk of development of future melanoma
- Morphological Changes in Human Scalp Hair Roots during Deprivation of Protein
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A second <i>KRT</i>71 allele in curly coated dogs
- The role of hair follicles and Edar signalling in cutaneous wound healing
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia
- Electrolysis and thermolysis for permanent hair removal
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- A Contemporary View on Felix Pinkus’ Concept of the Vitreous Membrane
- Tritiated Thymidine: Effect of Decomposition by Self-Radiolysis on Specificity as a Tracer for DNA Synthesis
- The hair shaft: normality, abnormality, and genetics
- Study on the expression patterns of inner root sheath-specific genes in Tan sheep hair follicle during different developmental stages
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Loose anagen hair syndrome
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Inherited Disorders of the Hair
- Facial Follicular Spicules: A Rare Cutaneous Presentation of Trichodysplasia Spinulosa
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Biology and Genetics of Hair
- Ectodermal Dysplasia: Variable Expressions