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Research 811–840 of 1000+
- Alopecia em pacientes anticoagulados
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Molecular Diagnostics and Control of Zoonotic Dermatophytosis: First Detection of Trichophyton indotineae in a Dog in Africa
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- The JAK/STAT signaling pathway: from bench to clinic
- The microbiome in patients with atopic dermatitis
- EMT Factors and Metabolic Pathways in Cancer
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization
- Pioneer factors govern super-enhancer dynamics in stem cell plasticity and lineage choice
- HOXC13 Is Involved in the Regulation of Human Hair Keratin Gene Expression
- Recurrent implantation failure: A comprehensive summary from etiology to treatment
- From regenerative dentistry to regenerative medicine: progress, challenges, and potential applications of oral stem cells
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Microneedles as transdermal drug delivery system for enhancing skin disease treatment
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- Hox genes in development and beyond
- Application of microneedle patches for drug delivery; doorstep to novel therapies
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- The Impact of Angiotensin-Converting Enzyme 2 (ACE2) Expression Levels in Patients with Comorbidities on COVID-19 Severity: A Comprehensive Review
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Functional Enhancers As Master Regulators of Tissue-Specific Gene Regulation and Cancer Development.
- Spatiotemporal Expression, Distribution, and Processing of POMC and POMC-derived Peptides in Murine Skin