Search
for
Sort by
Research 571–600 of 1000+
- Indian Hedgehog Controls Proliferation and Differentiation in Skin Tumorigenesis and Protects against Malignant Progression
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- LB1053 Dysregulation of antioxidant enzyme PRDX5 in alopecia areata
- Prolactin: A Mammalian Stress Hormone and Its Role in Cutaneous Pathophysiology
- 320 An open label clinical trial of Abatacept (CTLA4-Ig) for alopecia areata
- G.P.2.16 Valproate, acetylcarnitine, folic acid and vitamin B12 in spinal muscular atrophy: Preliminary data of an open-label study in children
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- Technical note: A comparison of DNA collection methods in cattle and yaks1
- Increased PHGDH expression uncouples hair follicle cycle progression and promotes inappropriate melanin accumulation
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Gab1 and Mapk Signaling Are Essential in the Hair Cycle and Hair Follicle Stem Cell Quiescence
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- ACE2 and TMPRSS2 Potential Involvement in Genetic Susceptibility to SARS-COV-2 in Cancer Patients
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- The Association of Gene Expression and Single Nucleotide Polymorphism (rs 6152 SNP) in Androgen Receptor Gene with Recurrent Spontaneous Abortion (RSA) in Iraqi Women
- 307 Computer-assisted epitope prediction revealed potential autoantigens associated with human alopecia areata
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- 1270 Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia