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Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

A new method was developed to accurately detect and measure 47 different drug ingredients in various products.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

A new method accurately measures long-term hormone levels in hair.

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

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

TRASER effectively targets blood vessels and hair follicles for potential use in vascular and hair removal treatments.

Two new gene mutations cause a rare hair disorder.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Method can accurately measure five BPH drugs at once.

Higher CSF 5-HIAA levels may predict better response to serotonin re-uptake inhibitors in trichotillomania.

SAHA syndrome links oily skin, acne, excess hair, and hair loss in women, similar to PCOS.

Laser therapy on human skin affects the HERC6 gene and related genes, influencing many cell processes and requiring careful safety measures.

The UHS promoter is specific to mouse hair follicles.

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

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Loose anagen hair syndrome in children often resolves on its own.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Lower 2D:4D finger ratios in HS patients suggest prenatal hormone influence on the disease.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

A new method creates valuable compounds for drug discovery by breaking traditional chemical rules.

A new method accurately measures nine neuroactive steroids in small blood samples, helping to study brain diseases.