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Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

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.

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.

Experts met to improve care for ichthyosis patients in Spain.

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

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

A 5-year-old Akita with a rare skin condition improved significantly after treatment.

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

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

sPLA2-X is crucial for normal hair growth and follicle health.

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

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

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

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.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

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.

Hairless gene not strongly linked to baldness.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Early onset hair loss linked to genetics and androgen levels.