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Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Plucked hair follicles can help diagnose scalp lupus.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

ILC1-like cells can cause alopecia areata by disrupting hair follicle immunity, suggesting a new treatment approach.

Hairless protein can block vitamin D activation in skin cells.

Scientists discovered two versions of a new human hair keratin gene.

PD‐L1 and PD‐L2 may not effectively control immune activation in alopecia areata.

Black hairy tongue can be an early sign of graft-versus-host disease after stem cell transplants.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

Belatacept may be a promising treatment for alopecia areata.

There is a significant need for better-validated quality of life tools in dermatology.

New genetic mutations causing hair loss were found in a Chinese family.

Hairless gene not strongly linked to baldness.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

SLHA can be hard to diagnose and needs teamwork between specialists.

CD44 variant changes start alopecia areata, but don't maintain it.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

MCHR2 gene duplications may be linked to alopecia areata.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.