Search

everythinglearnresearchcommunity

for

Search:↓

SIPHL1 from tomato enhances plants' response to low phosphate levels.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Genetic profiling can improve androgenetic alopecia treatment by predicting drug response and minimizing side effects.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Increased PHGDH expression causes early melanin buildup in hair follicles.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Everyone has an immune response to PPD, but reactions differ, causing tolerance, mild inflammation, or allergy.

Certain genetic markers may increase or decrease prostate cancer risk.

A girl had rickets due to a gene mutation affecting vitamin D response.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Gene differences affect finasteride side effects in men with hair loss.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Two siblings have a rare hair condition caused by a new genetic variant.

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

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

A hereditary condition causes hair loss and twisted hair in some family members.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Gene variations may increase oxidative stress in male pattern baldness.

No significant link was found between the studied genes and female hair loss in the Polish population.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.