Search
for
Sort by
Research 31–60 of 1000+
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Ectodermal Organ Stem Cells: Morphogenesis, Population Regenerative Behavior, and Evo-Devo
- Hair Follicle Organoids Using Human iPSC-Derived Ectodermal Precursor Cells for Hair Regenerative Medicine
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Ectodermal Dysplasia: Variable Expressions
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Genetic characterization of congenital defects in dogs : caudal dysplasia, ectodermal dysplasia and mucopolysaccharidosis VII
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Scarring Folliculitis in the Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Functional ectodermal organ regeneration as the next generation of organ replacement therapy
- 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
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Tissue expansion for correction of alopecia in a child with hypohidrotic ectodermal dysplasia