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All-trans retinoic acid causes hair loss by increasing TGF-β2 in hair follicle cells.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

Adrenal disorders can cause lasting brain and behavior issues in children.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Genetic marker rs12558842 strongly linked to male hair loss.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

Gene linked to common hair loss found, may lead to new treatments.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Stem cells help remove dead cells to keep tissues healthy by balancing cell replacement and clearance.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

The girl's condition improved with treatment, showing no new autoimmune diseases and hair regrowth.