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Research 91–120 of 1000+
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Alopecia: possible causes and treatments, particularly in captive nonhuman primates.
- Hox genes in development and beyond
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Frontiers in Topical Photoprotection
- What does the research say about androgen use and cerebrovascular events?
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Hair follicle-derived epithelial sheet has potential in vitiligo treatment
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- MICRO-URZĄDZENIA, BEZPRZEWODOWE KAPSUŁKI, MAPY, STYMULATORY I ROZRUSZNIKI STOSOWANE DO DIAGNOSTYKI I LECZENIA ZABURZEŃ MOTORYKI PRZEWODU POKARMOWEGO
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- The Causes of Hair Loss in Women 20-30 Years Old
- Pharmacology of anabolic steroids
- Skin wound healing in humans and mice: Challenges in translational research
- The PDGF/PDGFR pathway as a drug target
- Bioengineering a 3D integumentary organ system from iPS cells using an in vivo transplantation model
- Follicular dermal papilla structures by organization of epithelial and mesenchymal cells in interfacial polyelectrolyte complex fibers
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- The mRNA for Protease Nexin-1 is Expressed in Human Dermal Papilla Cells and its Level is Affected by Androgen
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Targeting host cell proteases as a potential treatment strategy to limit the spread of SARS‐CoV‐2 in the respiratory tract
- Congenital atrichia and hypotrichosis
- Biotinidase deficiency characterized by skin and hair findings
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases