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

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

The document concludes that gender-affirming treatments are essential for transgender individuals and outlines safe hormone therapy practices.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Dihydrotestosterone (DHT) is crucial for conditions like male-pattern baldness and acne, and measuring a byproduct, androstanediol glucuronide, is a better way to assess DHT's effects than DHT blood levels.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

New drug shows promise for better hair growth in baldness treatment.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

A three-year-old girl has hair loss despite treatment with selenium sulfide shampoo and anti-fungal medication.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

More research is needed to understand sex and racial differences in long COVID.