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Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

Many COVID-19 patients have long-term symptoms, especially women, but certain medications may help reduce these symptoms.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Early skin biopsy helps diagnose and manage severe skin conditions in babies.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Fetal skin cells from a cell bank heal wounds faster and with less scarring than adult cells.

SHBG may be a useful early indicator and treatment target for PCOS.

Female pattern hair loss is common, linked to polycystic ovarian syndrome, and treated with topical Minoxidil.

New cells are added to the hair's dermal papilla during the active growth phase.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Measuring reproductive hormones in brown bear hair could help identify their sex and reproductive state, but better collection methods or lab techniques are needed.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Adult stem cells with Tp63 can form hair and skin cells when placed in new skin, showing they have hidden abilities for skin repair.

Androgenic Alopecia, a common hair loss condition, can be effectively treated with finasteride and other treatments.

The proteins transthyretin and megalin are more present in the growth phase of hair, suggesting they might affect hair health and growth.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Aleglitazar and its major metabolite are safe enough to proceed to Phase 3 clinical trials.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

No single biomarker is reliable enough for diagnosing and assessing SLE.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The document concludes that understanding health requires considering evolutionary perspectives on reproductive fitness, and recognizing the complexity of factors like diet, testosterone, and sexual orientation.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

Skin issues can indicate immune system problems.