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Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Neoplasms hide in hair follicles to avoid the immune system.

A woman with severe hair loss was successfully treated with the drug adalimumab.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

Root hairs in cereal crops can grow beyond the usual zone, and using Turface® clay helps study this.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Certain fats in the blood are linked to an increased risk of male pattern baldness.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

FGF5 gene mutations cause long hair in domestic cats.

Myositis in lupus patients is linked to skin rash, hair loss, blood issues, and high disease activity.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Heat treatment increases hair loss in certain mice.

GDNF helps grow hair and heal skin wounds by acting on hair stem cells.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

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

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

Certain hairstyles, diabetes, scalp infections, and vitamin D deficiency may increase the risk of hair loss in Black women; more research is needed for better treatment.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The conclusions are: fecal short-chain fatty acids may help prevent cancer, fiber intake can reduce obesity, weight loss is hard for obese people, low BMI cancer patients are more prone to chemotherapy side effects, intermittent fasting benefits gut health, cherry laurel has health benefits in rats, certain gene variations can increase stress in hair loss patients, fecal acids can affect blood sugar levels, cold agglutinin can affect blood test results in autoimmune patients, and people with Crohn's disease have higher levels of a certain chemical in their blood.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

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

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

New genetic locations explain much of hair color variation in Europeans.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.