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Research 151–180 of 159
- Alopecia in Epidermolysis Bullosa
- Type 1 interferon signature and cytotoxic T lymphocyte activation targeted against sweat ducts in inflammatory acquired idiopathic generalized anhidrosis
- KID Syndrome: Report of a Case and Support for Its Reclassification as an Ectodermal Dysplasia
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Sweat under surveillance: Loss of immune–metabolic loop during aging
- The Role of Vitamin D and Testosterone Levels with Hair Loss among Females with Coronavirus Disease
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Edar Signaling in the Control of Hair Follicle Development
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- The Roles of EDA2R in Ageing and Disease
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Biology and Genetics of Hair
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- Ectodysplasin research—Where to next?
- Inherited Disorders of the Hair
- Current Genetics in Hair Diseases