Search
for
Sort by
Research 451–480 of 1000+
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Poster Presentations
- Symptomatic zinc deficiency in a full-term breast-fed infant
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- A rare cutis verticis gyrata secondary to cerebriform intradermal nevus: case report and literature review
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Ptosis in childhood
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Bifidobacterium Is Enriched in Gut Microbiome of Kashmiri Women with Polycystic Ovary Syndrome
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Cannabinoid Compounds as a Pharmacotherapeutic Option for the Treatment of Non-Cancer Skin Diseases
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- The Pharmacology of Regenerative Medicine
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Madarosis: A marker of many Maladies