Search
for
Sort by
Research 541–570 of 1000+
- A novel eco-friendly Acinetobacter strain A1-4-2 for bioremediation of aquatic pollutants
- Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reason
- De novo assembly and annotation of Asiatic lion (<i>Panthera leo persica</i>) genome
- Comparison of Effects on Gene Expression Activity of Low-Molecular-Weight Lychee Fruit Polyphenol (Oligonol®), Adenosine, and Minoxidil in Human Dermal Papilla Cells
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- Hair follicle gene expression profiling in the SubPopulations and InteRmediate Outcome Measures in COPD Study (SPIROMICS)
- Down-Stream molecular Responses to Volatile Signaling in Roots
- FGF5 is a crucial regulator of hair length in humans
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- Sarcoptic mange outbreak decimates South American wild camelid populations in San Guillermo National Park, Argentina
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- A new type of pachyonychia congenita.
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Alopecia: Association with Resistance to Thyroid Hormones
- A newborn presenting with congenital blistering
- A Case of Tinea Capitis Caused by Trichophyton tonsurans.
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- An adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa
- Forensic skeletal and molecular anthropology face to face: Combining expertise for identification of human remains
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
- Two siblings with uncombable hair syndrome: A new pathogenic variant
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma