Search
for
Sort by
Research 31–60 of 1000+
- Beyond Expectations
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Historical and Current Adenosine Receptor Agonists in Preclinical and Clinical Development
- The Role of Histone Demethylases in Disease
- Cell wall-associated ROOT HAIR SPECIFIC 10, a proline-rich receptor-like kinase, is a negative modulator of Arabidopsis root hair growth
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- The Harmonies Played by TGF-β in Stem Cell Biology
- Hair loss after covid 19 - case series
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Trichoscopy in Hair Shaft Disorders
- Monilethrix Treated with Minoxidil
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Inherited Disorders of the Hair
- Dendrobium officinale polysaccharide improves hair regrowth in androgenetic alopecia mice and is associated with coordinated changes in local steroid metabolism, ESR1 activation, and keratin-related follicular responses
- Transcriptome Dynamics Reveal Stage-Specific and Melatonin-Triggered Gene Expression Patterns During The Cashmere Growth Cycle in Capra Hircus
- The human keratins: biology and pathology
- Keratin disorders: from gene to therapy
- Disorders of hair in children
- The PDGF/PDGFR pathway as a drug target
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Androgen receptors and their biology
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Applications and Risks of Nanomaterials Used in Regenerative Medicine, Delivery Systems, Theranostics, and Therapy
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Molecular Genetics of Alopecias
- A Case Report of Werner’s Syndrome With a Novel Mutation From India