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Research 91–120 of 1000+
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Genome-wide detection and sequence conservation analysis of long non-coding RNA during hair follicle cycle of yak
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Multiple cyclic nucleotide‐gated channels coordinate calcium oscillations and polar growth of root hairs
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Diagnostic approach to low‐renin hypertension
- The endocrinology of baldness
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia
- Single-Cell Sequencing Technology in Ruminant Livestock: Challenges and Opportunities
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata
- Evolving approaches to profiling the microbiome in skin disease
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- Integration Analysis of Transcriptome Sequencing and Whole-Genome Resequencing Reveal Wool Quality-Associated Key Genes in Zhexi Angora Rabbits
- Single-Cell RNA Sequencing Reveals Cellular and Transcriptional Changes Associated With M1 Macrophage Polarization in Hidradenitis Suppurativa
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Construction of transcriptome atlas of white yak hair follicle during anagen and catagen using single-cell RNA sequencing
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study