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Research 61–90 of 1000+
- Feather arrays are patterned by interacting signalling and cell density waves
- What does acne genetics teach us about disease pathogenesis?
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- ARHGEF3 Regulates Hair Follicle Morphogenesis
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Molecular Regulatory Mechanisms in Chicken Feather Follicle Morphogenesis
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Tissue Regeneration, Stem Cells, and Wound Healing
- Study of seed hair growth in Populus tomentosa, an important character of female floral bud development
- Causal links between 13 autoimmune diseases and graft dysfunction: A Mendelian randomization study
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Evaluation of the Hair Growth-Promoting Effects of Combined Treatment with Hair Growth Stimulants
- FGF5 is a crucial regulator of hair length in humans
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Identification of functional circRNAs regulating ovarian follicle development in goats
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- TRPV3 Ion Channel: From Gene to Pharmacology
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#