Search

everythinglearnresearchcommunity

for

Search:↓

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

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

Certain gene variations are found in people with polycystic ovary syndrome.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Two new gene mutations cause a rare hair disorder.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

The G allele of IFITM3 rs12252 is linked to more severe COVID-19.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

Genetic variations may affect how well finasteride works for BPH patients.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

These gene variations are not linked to alopecia areata in Egyptians.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Male pattern baldness is linked to specific genetic variations in the androgen receptor gene.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Different forms of finasteride dissolve and remain stable differently, affecting capsule quality.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

CT60 polymorphism might increase the risk of Alopecia Areata.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.