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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

FOXN1 gene variants cause low T cells and immune issues from birth.

Dental pulp stem cells are better for tissue repair, while fat tissue stem cells may be more suited for wound healing and hair growth.

Hair follicle stem cells change states with age, affecting hair growth and aging.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Scientists found a new method using 3D cell cultures to grow human hair which may improve hair restoration treatments.

Ruxolitinib effectively regrows hair in most patients with severe hair loss.

Skin-derived precursors in hair follicles come from different origins but function similarly.

M2 macrophages help hair regrowth in wounds by making growth factors.

The trial aims to understand how obesity and lifestyle affect circadian rhythms in people with schizophrenia and bipolar disorder.

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

The study concluded that hair growth in mice is regulated by a stable interaction between skin cell types, and disrupting this can cause hair loss.

Coloring shampoos for gray hair may cause gene mutation, reproductive issues, and skin damage, needing stricter regulation and expert consultation.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

Coenzyme Q10 helps reduce aging in human hair.

Scientists have developed a method to keep chicken feather follicles alive and structurally intact in a lab for up to a week.

Basal cell carcinomas may differentiate similarly to hair follicles and could be influenced by hair cycle-related treatments.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.