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Research 511–540 of 1000+
- Phosphorus-induced change in root hair growth is associated with IAA accumulation in walnut
- Structural Abnormalities in the Hair of a Patient with a Novel Ribosomopathy
- Circadian rhythm sleep-wake disorders (CRSWDs): Linking circadian misalignment to adverse health outcomes.
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Skin regional specification and higher-order <i>HoxC</i> regulation
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
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- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Attenuated PER3 amplitude in hair follicles is associated with sleep irregularity in schizophrenia
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Investigating the role of obesity, circadian disturbances and lifestyle factors in people with schizophrenia and bipolar disorder: Study protocol for the SOMBER trial
- The role of hsa‐miR‐193a‐5p as an important factor for control of inositol in alopecia areata
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Hair follicle associated pluripotent (HAP) stem cells jump from transplanted whiskers to pelage follicles and stimulate hair growth
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Distinct transcriptomic landscapes of cutaneous basal cell carcinomas and squamous cell carcinomas
- Defining the identity of mouse embryonic dermal fibroblasts
- Symptomatic zinc deficiency in a full-term breast-fed infant