Search

everythinglearnresearchcommunity

for

Search:↓

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

The hair loss in Belgian Blue crossbred calves was caused by a diet issue, not by disease or infection.

The rash on the infant indicated a serious underlying condition.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Keratin mutations cause skin diseases and could lead to new treatments.

New therapies are being developed that target integrin pathways to treat various diseases.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Notch signaling disruptions can cause various skin diseases.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

Colchicine might help treat different skin diseases, but more research is needed to confirm its effectiveness and safe dosage.

The AVET system effectively delivers genes to human keratinocytes and may help treat skin diseases.

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

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

When skin blisters, healing the wound is more important than growing hair, and certain stem cells mainly fix the blisters without helping hair growth.

Women with PCOS have more Bifidobacterium in their gut compared to those without PCOS.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Retinoids are effective for various skin conditions and hair loss but have serious side effects, so low doses are recommended.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

People with hair loss conditions may also have thyroid disorders, but more research is needed to understand the connection.

Some women with PCOS have rare genetic variants linked to the condition.

The research found specific genes and pathways that control fur development and color in young American minks.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Different types of PCOS need specific diagnosis methods and treatments.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

5-alpha reductase deficiency leads to male sexual development issues and treatments like finasteride help with prostate enlargement and hair loss.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

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