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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Finasteride potentially treats hair loss by reducing DHT production.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

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

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Different types of PCOS in Chinese Han women show varying levels of male hormone and metabolic issues.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Managing PCOS is hard because it varies a lot, treatments are limited, and there's a lot of false information online.

Type XVII collagen may help prevent skin aging.

Type XVII collagen helps control skin cell growth and may have anti-aging effects.

Type XVII collagen helps control skin cell growth and could be a target for anti-aging treatments.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Fibroblasts are crucial for tissue repair and inflammation, and understanding them can help treat fibrotic diseases.

The document concludes that diagnosing PCOS requires a thorough approach, considering various symptoms and risks, and calls for improved methods to identify PCOS types and prevent diabetes.