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Male hair loss is mainly due to thinner hair, not less hair.

More research is needed to confirm if laser therapy effectively treats hair loss.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

The document provides a method to classify human hair growth stages using a model with human scalp on mice, aiming to standardize hair research.

A woman with Castleman's disease died from respiratory failure due to bronchiolitis obliterans.

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

The conclusion is that proper signaling is crucial for hair growth and development, and errors can lead to cancer or hair loss.

A specific genetic deletion in goats affects cashmere yield and thickness.

Stem cells in the hair follicle are regulated by their surrounding environment, which is important for hair growth.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Patients treated in Respiratory Intensive Care Units for COVID-19 are more likely to get mood disorders than those in other care settings.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Using focused ultrasound on the brain can help epilepsy medicine work better in rats.

New research shows that skin diversity is influenced by different types of dermal fibroblasts and their development, especially involving the Wnt/β-catenin pathway.

Epithelial-mesenchymal interactions control hair growth cycles through specific molecular signals.

The document concludes that skin stem cells are important for hair growth and wound healing, and could be used in regenerative medicine.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

The Wnt/β-catenin pathway is important for tissue development and has potential in regenerative medicine, but requires more research for therapeutic use.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Neuregulin3 affects cell development in the skin and mammary glands.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.