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Research 211–240 of 1000+
- Alopezien und Hypotrichosen im Kindesalter
- Analogs of human genetic skin disease in domesticated animals
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- O05 Distinct epidermal cell populations and single-cell gene expression signatures are associated with <i>Staphylococcus aureus</i> in atopic dermatitis
- Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds
- Functional analysis of the PIP5K1A gene in Liaoning Cashmere goats: an investigation based on bioinformatics, tissue localization, and biological functions
- Investigating RNA-Seq-based differential gene expression during hair follicle development in Angora goat skin
- Photobiomodulation and its influence on the regulation of gene expression in human cells: a narrative literature review
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- TLR3 Activation Stimulates Autophagy Gene Expression in Keratinocytes
- Identification of Biomarkers in Affected Hair Follicles from Chronic Discoid LupusErythematosus by Weighted Gene Co-Expression Network Analysis
- Short Peptides Induce Development of Root Hair Nicotiana tabacum
- Mechanisms that regulate androgen receptor transcriptional activity
- Gene expression patterns during palatal shelf fusion
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- DEFINING THE ROLE OF ABI1 GENE IN PROSTATE CANCER PROGRESSION AND TREATMENT RESISTANCE
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Expression of the guinea-pig alpha-lactalbumin gene in transgenic mice
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Wound Healing and Skin Regeneration
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- THE PATHOGENESIS OF ALOPECIA AREATA
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Calcitonin gene‐related peptide (CGRP) may award relative protection from interferon‐γ‐induced collapse of human hair follicle immune privilege
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Osteopontin Gene is Expressed in the Dermal Papilla of Pelage Follicles in a Hair-Cycle-Dependent Manner
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes