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Research 901–930 of 1000+
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Uterus Hyperplasia and Increased Carcinogen-Induced Tumorigenesis in Mice Carrying a Targeted Mutation of the Chk2 Phosphorylation Site in Brca1
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Cicatricial (Scarring) Alopecias
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Connexin mutations in human disease
- Detection of five substitution TPO mutations in Polycystic Ovary Syndrome (PCOS) and thyroid hormones disturbance patients
- The Shaven (Sha) Mutation, Chromosome 15
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Novel mutation in PTCH1 gene in a patient with basal cell nevus syndrome and uterus bicornis
- Molecular Genetics of Human Hair Diseases
- Androgenetic Alopecia in Men: An Update On Genetics
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Stem cells and aberrant signaling of molecular systems in skin aging
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa