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AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Finding functions for unknown GPCRs is hard but key for making new drugs.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Genetic mutations linked to ectodermal dysplasias and hair loss were identified in Pakistani families.

Hair loss in Lichen Planopilaris is caused by immune system issues damaging hair follicles and stem cells.

Kawasaki Disease is rare and often missed in adults, who show different symptoms than children, and may benefit from early treatment.

Some women with PCOS have rare genetic variants linked to the condition.

PAR-1 may play a role in hair growth regulation in human hair follicles.

Potassium channel modulators mostly increase the activity of rat whisker mechanoreceptors.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Cepharanthine can potentially treat gastric cancer by stopping tumor growth.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Hair follicle keratin may have been used in tooth enamel evolution.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

UBC13 and UBC22 enzymes are important for plant growth and development in Arabidopsis thaliana.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Human keratinocytes do not naturally respond to androgens.

Two Australian Poll Hereford calves had severe anaemia, abnormal red blood cells, and skin issues.

ERULUS is crucial for root hair growth by controlling calcium levels.

SPARC likely aids in tissue remodeling during the hair cycle, not in starting new hair growth phases.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

ATP-sensitive potassium channels play a role in chloroquine-induced itch in mice.