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Research 151–180 of 1000+
- Developmental genetics of color pattern establishment in cats
- Stem cell rejuvenation and the role of autophagy in age retardation by caloric restriction: An update
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Mucosal TLR5 activation controls healthspan and longevity
- Efficient Editing of CSLD2 Orthologue by CRISPR/Cas9 Affects Cell Morphogenesis of Root Hair in Spinach
- Functional Characterization of<i>fer-ts</i>, a Temperature-Sensitive FERONIA Mutant Allele That Alters Root Hair Growth
- Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
- Gene Variant in Amish a Clue to Better Aging
- 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Pilot study: genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia.
- 131 Mutational landscape of extramammary Paget disease
- Hairless: A nuclear receptor corepressor essential for skin function
- Tracing the cellular origin of cancer
- Ultraviolet Radiation in Wound Care: Sterilization and Stimulation
- The Transcriptional Co-Activator cAMP Response Element-Binding Protein-Binding Protein Is Expressed in Prostate Cancer and Enhances Androgen- and Anti-Androgen-Induced Androgen Receptor Function
- Genetics of Structural Hair Disorders
- Targeting receptor–regulator interactions
- Chaperones as thermodynamic sensors
- ATP-competitive mTOR kinase inhibitors delay plant growth by triggering early differentiation of meristematic cells but no developmental patterning change
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Molecular Regulation of Melanocyte Senescence
- Influence of TRPV3 mutation on hair growth cycle in mice
- 46,XY DSD due to impaired androgen production
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS