Search
for
Sort by
Research 811–840 of 1000+
- Spreading of Isolated Ptch Mutant Basal Cell Carcinoma Precursors Is Physiologically Suppressed and Counteracts Tumor Formation in Mice
- Long-read RNA sequencing reveals extensive transcript isoform changes in a patient with IFAP syndrome with a recurrent intronic MBTPS2 variant
- Hypomyelinating leukodystrophy-10 presenting with an additional atypical feature of increased body hair and Mongolian spots
- Cutaneous epitheliotropic T‐cell lymphoma in a sugar glider (<i>Petaurus breviceps</i>)
- SUBSTYTUCJA EGZOGENNYCH CHOLINESTERAZ W LECZENIU CIĘŻKICH ZATRUĆ ZWIĄZKAMI FOSFOROORGANICZNYMI
- In vitro strategies for mimicking dynamic cell–ECM reciprocity in 3D culture models
- Melatonin Modulates Tomato Root Morphology by Regulating Key Genes and Endogenous Hormones
- 851 The role of astrotactin2 in regulating mammalian skin polarity
- Chemically Induced Hair Loss/Alopecia
- Effects of Biomaterials Derived from Germinated Hemp Seeds on Stressed Hair Stem Cells and Immune Cells
- The effects of androgens on drug metabolism and transport: clinical pharmacologic considerations for people assigned female at birth
- Reproductive performance of hair ewes and rams implanted with Melatonin previous to the anestrus season in Northwest Mexico
- From signal to form: aspects of the cytoskeleton-plasma membrane—cell wall continuuum in root hair tips
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Iatrogenic androgenetic alopecia in a male phenotype 46XX true hermaphrodite
- Mason gastric bypass
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Repigmentation of Gray Hair After Thyroid Hormone Treatment
- LB1053 Dysregulation of antioxidant enzyme PRDX5 in alopecia areata
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Structure of human type II 5 alpha-reductase gene.
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma
- Heparan Sulfate Regulates Hair Follicle and Sebaceous Gland Morphogenesis and Homeostasis
- Ethanol intake patterns in female mice: Influence of allopregnanolone and the inhibition of its synthesis
- Nephronectin is Correlated with Poor Prognosis in Breast Cancer and Promotes Metastasis via its Integrin-Binding Motifs
- Comparative Transcriptome Analysis Reveals that a Ubiquitin-Mediated Proteolysis Pathway Is Important for Primary and Secondary Hair Follicle Development in Cashmere Goats