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YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Mice with CBS deficiency are healthier on a low-methionine diet.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Topical immunotherapy with DPCP is most effective for certain alopecia areata types, with success linked to age and disease duration, and influenced by a gene polymorphism.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Genetic variants affect minoxidil hair loss treatment success.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Researchers found two new genetic variants linked to Alzheimer's disease.

Genetic markers can help predict ear shapes for forensic use.

Certain VDR gene changes can affect melanoma risk.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Selenium imbalance can cause hair loss and skin issues.

Genetics, epigenetics, and lifestyle all influence facial skin aging.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

Polycystic ovary syndrome is a complex condition that affects women's mental, reproductive, and metabolic health throughout their lives.

Diet changes can protect against harmful environmental effects on fetal development.

Fat tissue stem cells may help increase hair growth.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Hormonal imbalances may play a role in frontal fibrosing alopecia, and antiandrogenic drugs combined with steroids are currently the most effective treatment.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Chemical exposure may contribute to the rise in atopic diseases and needs more research.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A man lost all his hair after stopping hepatitis C treatment and it didn't grow back.

4-O-methylhonokiol from Magnolia officinalis significantly promotes hair growth.

Melatonin may help with nerve pain, a hepatitis C drug is effective but has side effects, a treatment for mouth sores works but can cause blood issues, ear reconstruction with an implant is safe, HIV transmission from mother to child in Taiwan is now 0% with treatment, certain blood problems are more common in people with a tongue condition, a gene and being overweight are linked to hair loss in some women, a new technique could reduce radiation for lung nodule patients, a hepatitis treatment may lower cancer recurrence after a procedure, and adding extra screening improves tuberculosis detection in patients with lung infections.

Androgens may increase arrhythmias in Brugada Syndrome, while Finasteride could reduce them.

Higher EULAR/ACR scores in SLE patients predict more organ damage.