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Research 601–630 of 668
- The nude gene and the skin
- NG2 Proteoglycan Expression in Mouse Skin: Altered Postnatal Skin Development in the NG2 Null Mouse
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Evidence for 1,25-Dihydroxyvitamin D3-independent Transactivation by the Vitamin D Receptor
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Aggressive treatment in paediatric or young patients with drug-induced hypersensitivity syndrome (DiHS)/drug reaction with eosinophilia and systemic symptoms (DRESS) is associated with future development of type III polyglandular autoimmune syndrome
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Expression of the Orphan Protein Plet-1 during Trichilemmal Differentiation of Anagen Hair Follicles
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Expression and function of nuclear receptor co-activator 4: evidence of a potential role independent of co-activator activity
- Menopause, skin and common dermatoses. Part 2: skin disorders
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Expression Profiles of Reproduction- and Thyroid Hormone-Related Transcripts in the Brains of Chemically-Induced Intersex Frogs
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- DNA Damage-Inducible Transcript 4 Is an Innate Surveillant of Hair Follicular Stress in Vitamin D Receptor Knockout Mice and a Regulator of Wound Re-Epithelialization
- The Molecular Biology of the Vitamin D Receptor
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- AabHLH112, a bHLH transcription factor, positively regulates sesquiterpenes biosynthesis in Artemisia annua
- Epigenetic age estimation in saliva and in buccal cells
- The circular RNA circNlgnmediates doxorubicin-inducedcardiac remodeling and fibrosis
- Enhanced Sensitivity to Ethanol-Induced Inhibition of LTP in CA1 Pyramidal Neurons of Socially Isolated C57BL/6J Mice: Role of Neurosteroids
- Molecular interactions of progesterone derivatives with 5α-reductase types 1 and 2 and androgen receptors
- Epidermal Deletion of Rac1 Causes Stem Cell Depletion, Irrespective of whether Deletion Occurs during Embryogenesis or Adulthood
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis