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Research 181–210 of 1000+
- Dermatological complications due to post‑COVID‑19 syndrome: A systematic review
- Eyes open on stem cells
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Oral Presentations
- Bioengineered skin organoids: from development to applications
- Subject Index
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Cell death as an architect of adult skin stem cell niches
- SOX9 in organogenesis: shared and unique transcriptional functions
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Ectodermal Dysplasia: Variable Expressions
- Research Snippets
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- A new type of pachyonychia congenita.
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Connexin mutations in human disease
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Tissue expansion for correction of alopecia in a child with hypohidrotic ectodermal dysplasia