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Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Mitochondrial therapy and platelet-rich plasma therapy both stimulated hair regrowth in aging mice, with mitochondrial therapy showing similar effectiveness to plasma therapy.

Researchers found a gene mutation responsible for a rare hair loss condition.

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 human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Sex steroids affect the MafB gene differently in male and female hamsters.

Researchers found four genes that could help diagnose severe alopecia areata early.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Lactate production is important for activating hair growth stem cells.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Lack of cystatin M/E causes thin hair and dry skin.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Minoxidil can reduce functions related to androgen receptors.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

The SOSTDC1 gene is crucial for determining sheep wool type.