Search

everythinglearnresearchcommunity

for

Search:↓

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Some women with PCOS have rare genetic variants linked to the condition.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Tofacitinib citrate improved nail dystrophy and pain in patients with alopecia universalis without causing side effects.

Psoriasis skin changes are complex and might need several biopsies for a clear diagnosis.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

AR polyglycine repeat doesn't cause baldness.

AGA in children needs careful diagnosis due to low androgen levels and possible other causes.

Androstenedione is better than testosterone for diagnosing PCOS in Indian women.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Higher levels of β-carotene and vitamin E may help prevent certain types of hair loss.

Melanogenesis-related proteins may trigger immune responses in alopecia areata patients.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Common hair loss can be diagnosed with a physical exam and sometimes a hair test or skin biopsy, and treated with medication or surgery, with ongoing treatment needed to keep results.

The most common form of PCOS in the group was anovulatory PCOS, with no cases of obese PCOS, highlighting the importance of assessing lean women with menstrual issues.

Some early COVID-19 mutations in patients predicted future common virus mutations.

Most women with polycystic ovary syndrome (PCOS) have menstrual issues, infertility, acne, and excessive body hair, with the most common type being the non-androgenic phenotype.

COVID-19 may cause hair loss, often after recovery, with androgenetic alopecia being the most common type.

A 14-year-old boy is the youngest person reported with a rare, benign tumor related to hair follicles, usually found in older people.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Tofacitinib is effective and safe for severe hair loss, but full regrowth is less likely after 10 years of hair loss.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

PCOS is a common hormonal disorder in women that can affect skin, fertility, and metabolism, and treatment is tailored to individual needs.