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Research 541–570 of 802
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- The Wound Reporting in Animal and Human Preclinical Studies (WRAHPS) Guidelines
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Hair follicles modulate skin barrier function
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Application and Progress of Cultured Models of Gallbladder Carcinoma
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- t-Flavanone Improves the Male Pattern of Hair Loss by Enhancing Hair-Anchoring Strength: A Randomized, Double-Blind, Placebo-Controlled Study
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Testicular Steroidogenesis
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Expression and localization of Artemis serine 516 phosphorylation in human scalp skin
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- The exploration of mitochondrial‐related features helps to reveal the prognosis and immunotherapy methods of colorectal cancer
- TRPV3 Ion Channel: From Gene to Pharmacology
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Immunostaining study of cytokeratins in human hair follicle development
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Identification and single-cell analysis of prognostic genes related to mitochondrial and neutrophil extracellular traps in bladder cancer
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits