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MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The B2C promoter works in sheep cells but not in mouse embryos.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

KY19382 speeds up wound healing by activating a specific cell signaling pathway.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Double-stranded RNA helps regenerate hair follicles by increasing retinoic acid production and signaling.

Monilethrix is linked to a gene cluster on chromosome 12.

CD99 is highly present in certain skin cells and could help treat skin conditions.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

TLR2 helps control hair growth and regeneration, and its reduction with age or obesity can impair hair growth.

Overexpression of HDGF in melanocytes does not cause cancer.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

Vitamin D receptor helps control hair growth genes in skin cells.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Apple extract called procyanidin B-2 was found to greatly increase hair growth.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The Blood Glucose Management Service improved patient safety and outcomes in managing blood sugar in hospitalized patients.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.