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Research 571–600 of 1000+
- Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
- Prostate volume and its relationship with anthropometric variables among different ethnic groups of South-Kivu, DR Congo
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Regional Variation in Androgen Receptor Expression and Biomechanical Properties May Contribute to Cryptorchidism Susceptibility in the LE/orl Rat
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- 66-Year-Old Woman With Painless Vesicular Lesions
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
- Trailing the Path to Preventive Oncology
- Differentiating pulmonary lymphangioleiomyomatosis from pulmonary langerhans cell histiocytosis and Birt-Hogg-Dube syndrome
- Prevalence, Symptomatology and Herbal Management of Polycystic Ovarian Syndrome
- Immunogenetic and metabolic risk factors in male androgenetic alopecia: the role of HLA-DRB1 alleles and vitamin D3 deficiency
- Comparative Analysis of Chloroplast Genomes in Sansevieria Reveals Phylogenetic Relationships and High Variability Molecular Markers
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Understanding Polycystic Ovary Syndrome: A Comprehensive Guide
- E-Poster
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- An Infant with Worsening Rash
- Trichothiodystrophy in a child with occult learning disorder
- Role of Phenylalanine and Its Metabolites in Health and Neurological Disorders
- Prevalence of metabolic syndrome in the family members of women with polycystic ovary syndrome from North India
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage