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Research 211–240 of 1000+
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Biology and Genetics of Hair
- What causes hidradenitis suppurativa ?—15 years after
- Congenital hair loss disorders: Rare, but not too rare
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- Dihydrotestosterone inhibits hair growth in mice by inhibiting insulin-like growth factor-I production in dermal papillae
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Accelerated Endothelial to Mesenchymal Transition Increased Fibrosis via Deleting Notch Signaling in Wound Vasculature
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Construction of regulatory network for alopecia areata progression and identification of immune monitoring genes based on multiple machine-learning algorithms
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Acne
- A computationally inferred regulatory heart aging model including post-transcriptional regulations
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Tissue engineering of human hair follicles using a biomimetic developmental approach
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Treatment of MSCs with Wnt1a-conditioned medium activates DP cells and promotes hair follicle regrowth
- Genetically separable determinants of hair keratin gene expression