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A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Wnt-10b is important for keeping mouse skin cells healthy for hair growth.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

The document tests knowledge and decision-making in hematology through multiple-choice questions.

The document provides 70 multiple choice questions to improve haematology skills.

PRP is a safe natural treatment that improves skin by reducing wrinkles and enhancing texture for up to 4 months.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Patched1 helps prevent tumors by controlling cell growth.

Recent progress has been made in understanding inherited hair and nail disorders.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

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

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

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

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Genomic research can help improve the quality and production of natural fibers in animals.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Polycystic ovary syndrome and iron overload share similar symptoms and can be potentially treated with blood removal, diet changes, and probiotics.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.