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Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

Iron deficiency may contribute to hair loss.

New treatments for vitiligo may focus on protecting melanocyte stem cells from stress and targeting specific pathways involved in the condition.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Your genes, especially IL-1a, can predict how well a hair growth treatment with platelet rich plasma will work for you.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Androgenic alopecia in men is mainly linked to family history, hormonal imbalances, and metabolic issues, but can also be influenced by lifestyle habits, environmental factors, and deficiencies in certain vitamins and microelements like copper.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

Women with hirsutism have different levels of omentin-1, which may be linked to the condition and its genetic aspects.

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

Men with thinner hair from genetic hair loss may be more likely to have an enlarged prostate.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.