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Research 811–840 of 1000+
- Detection of five substitution TPO mutations in Polycystic Ovary Syndrome (PCOS) and thyroid hormones disturbance patients
- What is new in therapeutics?
- The condition of hair follicles produced by different punching methods during FUE surgery
- A Randomized Controlled Clinical Trial Protocol of Umbilical Cord Mesenchymal Stem Cell‐Derived Small Extracellular Vesicles for the Treatment of Androgenetic Alopecia in Young Males
- Dichotomy
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Differential expression of retinoic acid-synthesizing (RALDH) enzymes during fetal development and organ differentiation in the mouse
- Essential Oils and Their Single Compounds in Cosmetics—A Critical Review
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- From regenerative dentistry to regenerative medicine: progress, challenges, and potential applications of oral stem cells
- Potential Use of Human Periapical Cyst-Mesenchymal Stem Cells (hPCy-MSCs) as a Novel Stem Cell Source for Regenerative Medicine Applications
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Commitment of Oral-Derived Stem Cells in Dental and Maxillofacial Applications
- KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Hair organ regeneration via the bioengineered hair follicular unit transplantation
- Hair toxic and essential trace elements in children with autism spectrum disorder
- Receptor activator of NF-κB (RANK) stimulates the proliferation of epithelial cells of the epidermo-pilosebaceous unit
- The Role of Exosomes Derived From Mesenchymal Stromal Cells in Dermatology
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Induction of hair follicle dermal papilla cell properties in human induced pluripotent stem cell-derived multipotent LNGFR(+)THY-1(+) mesenchymal cells
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- The Role of Thymosin Beta 4 on Odontogenic Differentiation in Human Dental Pulp Cells
- Pain in Multiple Sclerosis: Understanding Pathophysiology, Diagnosis, and Management Through Clinical Vignettes
- Salivary gland function in persons with ectodermal dysplasias