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Research 331–360 of 660
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Effect of thyroid hormone and epidermal growth factor on tactile hair development and craniofacial morphogenesis in the postnatal rat.
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- The Fusion of Craniofacial Reconstruction and Microsurgery
- Factors affecting aesthetic results in patients undergoing craniofacial reconstruction following maxillofacial trauma
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- Lineage‐specific requirements of Alx4 function in craniofacial and hair development
- Advances and challenges in intravital imaging of craniofacial and dental progenitor cells
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Characterization of a mouse Scube3 reporter line
- Developmental Plasticity of Patterned and Regenerating Oral Organs
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- Botulinum Toxin for Scalp Conditions: A Systematic Review
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Possible Role of Osteopathic Manipulation Treatment in Alleviation of Finasteride-Induced Dementia through Modulation of HOMER-3 Gene Methylation
- The use of a retinoid receptor antagonist in a new model to study vitamin A-dependent developmental events.
- Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Assessing the Efficacy of Follicular Unit Extraction (FUE) in Beard and Moustache Transplants: A Comprehensive Analysis of 300 Cases
- Editorial highlights
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Forehead Anthropometrics of Jazan Population, Saudi Arabia: A Prospective Analytical Study
- Cooperation of TGF‐β and FGF signalling pathways in skin development
- Facial preservation following extreme mummification: Shrunken heads
- Multipotent Neural Crest Stem Cell-Like Cells from Rat Vibrissa Dermal Papilla Induce Neuronal Differentiation of PC12 Cells