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Research 841–870 of 1000+
- Clinical Management in Psychodermatology
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Malicious Mites—Sarcoptes scabiei in Raccoon Dogs (Nyctereutes procyonoides) in Schleswig-Holstein, Germany
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerism
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Modeling animal genomics in mice: An authentic approach for the functional interrogation of evolutionarily and agriculturally critical variants
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Development of a Predictive Model for Iron Levels in Bovine Muscle Tissue Using Hair as a Predictor
- Endocrine intervention for transsexuals
- Spatiotemporal dynamics of sensory neuron and Merkel-cell remodeling are decoupled during epidermal homeostasis
- Polycystic Ovary Syndrome: Etiology, Current Management, and Future Therapeutics
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Exploring the Complexities of Atopic Dermatitis: Pathophysiological Mechanisms and Therapeutic Approaches
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene