Search
for
Sort by
Research 301–330 of 1000+
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- Clonal expansion from standing genetic variation underpins the evolution of an emerging plant pathogen in Australia
- Erythema Nodosum Associated with Kerion: A Case Series and Narrative Review of the Literature
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Isolation and molecular characterization of Malassezia pachydermatis from a cutaneous lesion in a California sea lion (Zalophus californianus)
- Genetic effects of vascular endothelial growth factor and its receptor 2 on feather maturity in three chicken breeds
- Genetic Dissection of Leg and Back Feather Follicle Density in Yellow-feathered Broiler: Integrative GWAS and Transcriptome Analysis Reveal the Regulatory Role of SERPINF1
- The Telomerase Reverse Transcriptase (TERT) Gene Molecular Characterization in Sheep and the Association of Its Variation with Wool Traits
- Case Report: A case of Rothmund–Thomson syndrome-like phenotype with an ANAPC1 variant of uncertain significance and observed hair improvement
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- The Role of Vitamin D in Autoimmune Thyroid Diseases: From Immunomodulation to Clinical Implications
- The Rho GTPase regulator ARHGEF3 orchestrates hair placode budding by coordinating cell fate and P-cadherin patterning in mice
- Application of big data analytics in minoxidil drug development: a data-driven model for predicting efficacy and side effect risks
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Identification of Familial Infections Using Multilocus Microsatellite Typing in Tinea Corporis due to <i>Microsporum canis</i>
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq