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Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Black women's unique hair characteristics and styling practices can lead to specific scalp conditions, which require early diagnosis and appropriate treatment.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

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

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

Androgenetic alopecia in teens is linked to obesity and other metabolic risks, needing early diagnosis and management.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Girls conceived via assisted reproductive technologies show early puberty signs and larger ovaries.

Low HDL-C, uric acid, and 25-hydroxyvitamin D are risk factors for early-onset male hair loss.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Androgenetic alopecia in Nepalese men often starts around age 29, with a possible link to COVID-19 worsening the condition.

LGR5 helps maintain corneal cell characteristics and prevents unwanted changes by controlling specific cell signaling pathways.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

AGA is a genetic, hormonal hair loss treated with finasteride, minoxidil, and supplements, but new compounds are being developed.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

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

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Androgenetic alopecia is common in South-West Nigeria, affecting more men than women, with stress worsening the condition.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Wild African goats have genetic adaptations for surviving harsh desert conditions.