Search

everythinglearnresearchcommunity

for

Search:↓

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

S-1 treatment led to a complete response in pancreatic cancer with manageable side effects.

TSPO might help treat anxiety and depression.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Blocking 11β-HSD1 can lessen the harmful effects of glucocorticoids on hair growth cells.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Genomic prediction can improve breeding strategies for Korean Sapsaree dogs.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

The Gsdma3 gene is essential for normal hair development in mice.

UC.145 may be a new biomarker for predicting gastric cancer.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

The vitamin D receptor is involved in multiple body functions beyond calcium regulation, including immune response and rapid reactions not related to gene activity.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

Aging in one type of stem cell can cause aging-like changes in various organs.

SCD1 is crucial for skin health and overall energy balance.

HLD10 can include increased body hair and Mongolian spots.