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Research 481–510 of 1000+
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Role of skin enzymes in metabolism of topical drugs
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Androgen receptor gene polymorphism and biological age markers in men
- Prevalence Of Male Balding Pattern In Patient From Saveetha Dental College- Retrospective Comparative Evaluation Study
- Hashimoto Thyroiditis - A Comprehensive Review
- Fertility and Sterility Vol 101 No 4, April 2014
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Chronic overlapping pain conditions and nociplastic pain
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Keratin disorders: from gene to therapy
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle