Search
for
Sort by
Research 271–300 of 1000+
- 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達
- HAIR LOSS: CAUSES AND PATHOLOGY
- Covid-19 in Lupus Nephritis
- Hair Loss in Men and Women
- Hair and Scalp Variation Related to Gender
- Alopecia
- Subject Index
- Cutaneous Manifestations of Lupus Erythematosus
- Cutaneous signals of immune system disease
- Dermal white adipose tissue development and metabolism: The role of transcription factor Foxn1
- CXXC5: A novel regulator and coordinator of TGF-β, BMP and Wnt signaling
- Molecular mechanism for transcriptional regulation of the parathyroid hormone gene by Epiprofin
- Targeting of CXXC5 by a Competing Peptide Stimulates Hair Regrowth and Wound-Induced Hair Neogenesis
- Hair follicle epithelial stem cells contribute to interfollicular epidermis during homeostasis
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- GLI2 Is Expressed in Normal Human Epidermis and BCC and Induces GLI1 Expression by Binding to its Promoter
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- 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
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Cellular Senescence and Aging in Myotonic Dystrophy
- Dermal white adipose tissue: Development and impact on hair follicles, skin defense, and fibrosis
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome