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New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

ACTH may be an effective first-line treatment for acute calcium pyrophosphate crystal arthritis.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

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.

The conditions alopecia areata, primary sclerosing cholangitis, and ulcerative colitis may be linked by shared autoimmune and cell death mechanisms.

New protein changes may be involved in the immune attack on hair follicles in alopecia areata.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Fat tissue and a specific protein are crucial for healthy hair growth and maintenance.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

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

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

A man with multiple autoimmune diseases developed liver injury from azathioprine, but his liver improved after stopping the drug.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.

Redheaded people may have evolved to efficiently make vitamin D in areas with less sunlight.

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.