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Research 61–90 of 1000+
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Biology and Genetics of Hair
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Ectoderm-Targeted Overexpression of the Glucocorticoid Receptor Induces Hypohidrotic Ectodermal Dysplasia
- Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin
- Scarring Folliculitis in the Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
- ALX4-related frontonasal dysplasia sequence presenting with alopecia in a 12 year old girl
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- FC‐10 Adult‐onset hair loss in Chesapeake Bay retrievers: a clinical and histological study
- Inherited Disorders of the Hair
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome with Concomitant Lymphopenia: A Novel TP63 Mutation
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- EFFECT OF POTASSIUM ON BLOOD-SUGAR AND PLASMA-INSULIN LEVELS IN PATIENTS UNDERGOING PERITONEAL DIALYSIS AND HÆMODIALYSIS
- [Low dosage retinol and L-cystine combination improve alopecia of the diffuse type following long-term oral administration].
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Abnormal differentiation of epidermis in transgenic mice constitutively expressing cyclooxygenase-2 in skin
- Epidermal hyperplasia and oral carcinoma in mice overexpressing the transcription factor ATF3 in basal epithelial cells
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Congenital Atrichia: A Case Report
- [Trichothiodystrophy: a morphological and biochemical study].
- Age-associated inflammation connects RAS-induced senescence to stem cell dysfunction and epidermal malignancy
- Atrichia With Papular Lesions
- Noninflammatory, Nonpruritic Alopecia of Horses
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Coat Problems
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- A clinician's approach to canine alopecia
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor