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Research 571–600 of 1000+
- Edar Signaling in the Control of Hair Follicle Development
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle
- Assessment of vitamin D receptors in alopecia areata and androgenetic alopecia
- Molecular pathways involved in hair follicle tumor formation: all about mammalian target of rapamycin?
- Inducible expression of gasdermin A3 in the epidermis causes epidermal hyperplasia and skin inflammation
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Animal models and culture methods in the study of hair growth
- A new type of pachyonychia congenita.
- Comparison of hair manifestations in cardio‐facio‐cutaneous and Costello syndromes highlights the influence of the RAS pathway on hair growth
- <i>Hoxc13</i> and the development of hair follicle
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Pleiotropic effects of the nude mutation.
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- Developmental Genetics of Color Pattern Establishment in Cats
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Region-specific reversal of epidermal planar polarity in the <i>rosette</i> fancy mouse
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog
- The color of human hair
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Sparse Brittle Hair and Bilateral Temporal Alopecia in a Child