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The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Skin problems can be caused or worsened by physical forces and pressure on the skin.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

Swiss Holstein cattle with curly, short hair carry genes from the Simmental breed.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

A new mutation in the HR gene causes hair loss in a specific family.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Early onset hair loss linked to genetics and androgen levels.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Alopecia areata is an autoimmune disease causing hair loss, treatable with immune-modulating drugs, and linked to genetics.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

A specific gene mutation causes congenital hair loss.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Hair loss linked to prostate enlargement; stress and family history important factors.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Hyperandrogenism increases heart disease risk in premenopausal women, but this risk is linked to obesity in postmenopausal women.

Different hair loss patterns may be linked to varying male hormone levels.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.