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Research 91–120 of 1000+
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Murine skin as a target for melatonin bioregulation
- A Modeling Conundrum: Murine Models for Cutaneous Wound Healing
- Sequence and Expression of Murine Type I Hair Keratins mHa2 and mHa3
- Morphogenesis of chimeric hair follicles in engineered skin substitutes with human keratinocytes and murine dermal papilla cells
- Marie Antoinette Syndrome
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Bisbenzylisoquinoline Alkaloids from<i>Stephania cepharantha</i>and their Effects on Proliferation of Cultured Cells from the Murine Hair Apparatus
- Murine Cytomegalovirus is Not Associated With Alopecia Areata in C3H/HeJ Mice
- Effects of cepharanthine and minoxidil on proliferation, differentiation and keratinization of cultured cells from the murine hair apparatus
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Murine Vibrissae Cultured in Serum-Free Medium Reinitiate Anagen
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Alopecia areata and subsequent Marie Antoinette syndrome following COVID-19 infection and vaccination: A case report
- Clinically relevant aberrant Filip1l DNA methylation detected in a murine model of cutaneous squamous cell carcinoma
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Scanning electron microscopy of murine skin ultrathin sections and cultured keratinocytes
- Murine skin-derived multipotent papillary dermal fibroblast progenitors show germline potential in vitro
- Marie-unna hereditary hypotrichosis
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Murine Hair Follicle Derived Stem Cell Transplantation onto the Cornea Using a Fibrin Carrier
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Post‐Traumatic Tress Disorder: Obama, Palin and Marie‐Antoinette
- Marie Krogh's contributions to the study of thyroid physiology and pathophysiology