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Research 511–540 of 1000+
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- 848 Genes implicated in lipid & metabolic regulation downregulated in CCCA
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- 1392 Activation of Id2 gene regulatory network ruling quiescence of hair follicle stem cells
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Supplementary Material for: Effects of Food-Derived Collagen Peptides on the Expression of Keratin and Keratin-Associated Protein Genes in the Mouse Skin
- Supplementary Material for: Effects of Food-Derived Collagen Peptides on the Expression of Keratin and Keratin-Associated Protein Genes in the Mouse Skin
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Evolution in action: highlighting a role for the Agouti gene in development?
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- 026 Altered Skin Wound Healing in Homeobox Gene Msx-2 Knockout Mice
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Differential Gene Expression Screening Between Black and Gray Hairs Using Subtractive Library and DNA Chip
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- A Study of the androgen receptor gene polymorphism and the level of expression of the androgen receptor in androgenetic alopecia among Egyptians
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention
- Peripheral patterns of calcitonin‐gene‐related peptide general somatic sensory innervation: Cutaneous and deep terminations
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- Ectopic Expression of the nude Gene Induces Hyperproliferation and Defects in Differentiation: Implications for the Self-Renewal of Cutaneous Epithelia
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Decreased Androgen Receptor Gene Methylation in Premature Pubarche: A Novel Pathogenetic Mechanism?
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- Calcitonin gene‐related peptide (CGRP) may award relative protection from interferon‐γ‐induced collapse of human hair follicle immune privilege
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis