Search
for
Sort by
Research 901–930 of 1000+
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Cardiovascular risk markers in premature canities
- Classic versus non‐classic: A survival Kit for life in the skin
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Multimodal Reconstructive Treatment of the Face and Scalp Following Catastrophic Burn Injury: An Eight-Year Experience with Structural Fat Grafting, Follicular Unit Excision Hair Transplantation, and Scalp Micropigmentation
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Lichen Planus Pigmentosus as a Cutaneous Extrahepatic Manifestation of Chronic Hepatitis C Virus Infection: A Case Report
- Prevalence and Predictors of Premature Graying of Hair Before the Age of 30: A Cross‐Sectional Study in Saudi Arabia
- Analysis of Adverse Drug Reactions in Pediatric Patients with Epilepsy: An Intensive Pharmacovigilance Study
- Autologous stromal vascular fraction cells combined with platelet-rich plasma for androgenic alopecia treatment: a case series
- Vitiligo and alopecia areata: apples and oranges?
- The Overexpression of Tβ4 in the Hair Follicle Tissue of Alpas Cashmere Goats Increases Cashmere Yield and Promotes Hair Follicle Development
- Is age at puberty associated with semen quality and reproductive hormones in young adult life?
- Postpartum depression: Prevention and multimodal therapy
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Interrelationships between Skin Structure, Function, and Microbiome of Pregnant Females and Their Newborns: Study Protocol for a Prospective Cohort Study
- BMP2 and BMP7 play antagonistic roles in feather induction
- FGF signaling is required for initiation of feather placode development
- Adhesion Molecules in Skin Development: Morphogenesis of Feather and Hair<sup>a</sup>
- In ovo injection of CHIR-99021 promotes feather follicles development via activating Wnt/β-catenin signaling pathway during chick embryonic period
- Deadly hairs, lethal feathers – convergent evolution of poisonous integument in mammals and birds
- In Ovo Injection of CHIR-99021 Promotes Feather Follicle Development via Modulating the Wnt Signaling Pathway and Transcriptome in Goose Embryos (Anser cygnoides)
- Feather on the Cap of Medicine
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Genetic effects of vascular endothelial growth factor and its receptor 2 on feather maturity in three chicken breeds
- Dermo‐epidermal interactions in reptilian scales: Speculations on the evolution of scales, feathers, and hairs