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Research 181–210 of 1000+
- Stem Cell Competition for Niche Occupancy: Emerging Themes and Mechanisms
- Root hair specification and its growth in response to nutrients
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Autophagy protects murine preputial glands against premature aging, and controls their sebum phospholipid and pheromone profile
- Effects and Mechanism of Nutrients on Root Hair Growth
- Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation
- Integration of Ethylene and Auxin Signaling and the Developmental Consequences of Their Crosstalk
- 693 Dermal papilla-derived Wnt ligands are required for adult hair follicle growth
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- Differential metabolic adaptations define responses of winner and loser oncogenic mutant stem cells in skin epidermis<i>in vivo</i>
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Expression of lipid-protein gene PLP2 in Liaoning cashmere goat
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Vestibular Hair Cell Regeneration and Restoration of Balance Function Induced by Math1 Gene Transfer
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Effect of Adenovirus-Mediated Expression of Sonic Hedgehog Gene on Hair Regrowth in Mice With Chemotherapy-Induced Alopecia
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes