Search

everythinglearnresearchcommunity

for

Search:↓

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Certain genes are linked to the risk of developing Alopecia Areata.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

A new gene mutation causes a rare type of hair loss.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

A specific gene mutation causes congenital hair loss.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

A specific genetic variation affects wool quality in sheep.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Robertsonian translocation can cause recurrent miscarriages.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

The HCR gene contributes to psoriasis risk.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Variants on chromosome 10 affect hair thickness in Dazu black goats.