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A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Found new possible treatments for hair loss.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

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

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

Using special RNA to target a mutant gene fixed hair problems in mice.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

A new mouse mutation causes skin and hair defects due to a gene change.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Both vitiligo and alopecia areata involve an immune response triggered by stress and specific genes, with treatments targeting this pathway showing potential.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

New treatments targeting specific genes show promise for treating keratin disorders.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

A new mouse model for vitiligo helps study immune responses and potential treatments.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Mutant mice help researchers understand hair growth and related genetic factors.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

New treatments targeting T-cell pathways are needed for better alopecia areata management.