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Research 151–180 of 1000+
- Molecular characterization of GhPLDα1 and its relationship with secondary cell wall thickening in cotton fibers
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Increased lactate dehydrogenase activity is dispensable in squamous carcinoma cells of origin
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Tissue Retinol‐Binding Protein 4 Expression and Its Genetic Variants (rs3758539) in Patients With Severe and Treatment‐Refractory Alopecia Areata: Association With Response to Baricitinib
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- New developments in the molecular treatment of ichthyosis: review of the literature
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Abstracts
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Cell Proteomic Footprinting: Advances in the Quality of Cellular and Cell-Derived Cancer Vaccines
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- “Structural imprinting” of the cutaneous immune effector function
- Genetics of Inherited Ichthyoses and Related Diseases
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament