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Finasteride improves heart function and repairs damage after heart attack in mice.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Key genes linked to hair growth and cancer were identified in hairless mice.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Mice genetically modified to produce more CD109 in their skin had less inflammation and better healing with less scarring.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Hormone therapy for trans individuals is effective and generally safe in the short term.

NcoA4 may have roles beyond helping control gene activity, possibly affecting cell behavior and stability.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

A 3-month stay in space causes skin thinning, disrupts hair growth, and changes muscle-related genes in mice.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

Hair loss drugs may cause sexual issues and infertility in men.

Allopregnanolone changes gene expression in glioblastoma cells.

Older patients sticking to their prostate medication saw lasting health benefits.