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research Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies

4 citations , May 2023 in “Cells”

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

research Monilethrix in three generations

6 citations , January 2008 in “Indian Journal of Dermatology”

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

research Editor's evaluation: Crosstalk with keratinocytes causes GNAQ oncogene specificity in melanoma

August 2021

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

research Topical minoxidil improves congenital hypotrichosis caused by LIPH mutations

7 citations , March 2015 in “British Journal of Dermatology”

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

research Expression analysis of proteasome maturation protein (POMP) gene in Liaoning Cashmere goat

7 citations , April 2019 in “Animal biotechnology”

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

research Lgr6+ stem cells and their progeny in mouse epidermis under regimens of exogenous skin carcinogenesis, and their absence in ensuing skin tumors

7 citations , November 2016 in “Oncotarget”

UV exposure reduces Lgr6+ stem cells in mouse skin and they don't significantly contribute to skin cancer development.

research Genetic Ablation of the CDP/Cux Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility

97 citations , March 2002 in “Molecular and cellular biology”

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

research Discreet monilethrix: De novo mutation on the example of polish families

1 citations , January 2017 in “International Journal of Trichology”

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

research Monilethrix – Case report of a rare disease

January 2015 in “Nasza Dermatologia Online”

Monilethrix causes fragile, patchy hair loss.

research Piecing together the pigment-type switching puzzle

10 citations , November 2009 in “Pigment cell & melanoma research”

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

research Monilethrix

6 citations , August 2012 in “The Journal of Pediatrics”

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

research Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by LIPH Pathogenic Variants

5 citations , July 2020 in “JAMA Dermatology”

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.

The Feasibility and Utility of Hair Follicle Sampling to Measure FMRP and FMR1 mRNA in Children With or Without Fragile X Syndrome: A Pilot Study

research The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study

December 2022 in “Journal of neurodevelopmental disorders”

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

research Association Between Retinoid X Receptor Gene Variants and Dyslipidemia Risk in an Iranian Population

1 citations , September 2021 in “Cureus”

The rs1128977 gene variant may affect cholesterol and body measurements.

research State-dependent signaling by Ca_v1.2 regulates hair follicle stem cell function

27 citations , June 2013 in “Genes & development”

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

research 602 Sox13 is a novel marker for hair follicle development and differentiation

September 2019 in “Journal of Investigative Dermatology”

Sox13 is a new marker for early hair follicle development and differentiation.

Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature

research Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature

December 2024 in “Livers”

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

CRABP1 Enhances Proliferation of Dermal Papilla Cells in Hu Sheep via Wnt/β-Catenin Pathway

research CRABP1 Enhances the Proliferation of the Dermal Papilla Cells of Hu Sheep through the Wnt/β-catenin Pathway

September 2024 in “Genes”

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

research Nε-(carboxymethyl) lysine represses hair follicle formation by inhibiting Sonic hedgehog expression in a NF-κB-independent manner

January 2019 in “Proceedings for Annual Meeting of The Japanese Pharmacological Society”

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

research Synchronous profiling and analysis of mRNAs and ncRNAs in the dermal papilla cells from cashmere goats

17 citations , June 2019 in “BMC genomics”

Non-coding RNAs help control hair growth in cashmere goats.

Differential Expression of Keratin and Keratin-Associated Proteins Linked with Hair Loss in Spontaneously Mutated Inbred Mice

research Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice

July 2024 in “bioRxiv (Cold Spring Harbor Laboratory)”

Hair loss in certain mice is linked to changes in keratin-related genes.

research Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes

35 citations , August 2010 in “The American journal of pathology”

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.