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Research 601–630 of 1000+
- Comparison between topical cetirizine with minoxidil versus topical placebo with minoxidil in female androgenetic alopecia: a randomized, double-blind, placebo-controlled study
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Recent progress in the manipulation of biochemical and biophysical cues for engineering functional tissues
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- FOXN1 deficient nude severe combined immunodeficiency
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Oil body bound oleosin-rhFGF9 fusion protein expressed in safflower (Carthamus tinctorius L.) stimulates hair growth and wound healing in mice
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- Making the head: Caspases in life and death
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Oral Presentations
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Unraveling Translational Insights into Systemic Multi-Organ Toxicity of Cytosine Arabinoside (Ara-C): A Systematic Review of Preclinical Animal Evidence
- Cronkhite–Canada Syndrome With Multiple Mesenteric Lymphadenopathy: A Case Report
- Bioengineered skin organoids: from development to applications
- Editor's evaluation: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis
- Temporal Triangular Alopecia – A Diagnostic Dilemma: Case Series of Six Patients
- Converging physiological roles of the anthrax toxin receptors
- A 4kb Fragment of the Desmocollin 3 Promoter Directs Reporter Gene Expression to Parakeratotic Epidermis and Primary Hair Follicles
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Transgenic mice provide new insights into the role of TGF-alpha during epidermal development and differentiation.
- Low‐level laser (light) therapy (LLLT) for treatment of hair loss
- Cell fate decisions: emerging roles for metabolic signals and cell morphology
- Hox genes in development and beyond
- p63: a crucial player in epithelial stemness regulation
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development