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Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Hair length in rabbits is linked to differences in lipid metabolism and cell death.

T cells affect skin cell genes in inflammatory diseases, and therapy can normalize these changes.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

Sex hormones affect brain cells differently in males and females.

ING5 is crucial for stem cell maintenance and preventing certain cancers.

Developing microRNA-based treatments is hard but has potential.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.

Korean long-tailed chickens have unique genes valuable for ornamental breeding.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Certain genes in fat tissue affect weight loss in women with PCOS.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

Marine mammals lost many α-keratin genes, aiding their adaptation to aquatic life by becoming hairless.

Palate formation and skin healing share similar biological processes.

Testosterone treatment may change estrogen receptor methylation in AFAB individuals.

Chronic T. gondii infection may harm male fertility.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

SARS-CoV-2 may worsen IPF due to shared genes and pathways, suggesting potential drug targets.

rPanglaoDB helps study rare cell types by merging RNA data, showing fibrocytes aid in healing.

Researchers converted human embryonic stem cells into trophoblast stem cells using specific transcription factors.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

Thrombophilic conditions may worsen Long COVID symptoms due to increased blood clotting.