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research Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis

47 citations , September 2012 in “Human molecular genetics online/Human molecular genetics”

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

research Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients

31 citations , May 2021 in “Journal of endocrinological investigation”

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

research Central Centrifugal Cicatricial Alopecia Associated With PDL1 Loss and Increased Expression of Caspase 3: A Case Series

2 citations , April 2023 in “American Journal of Dermatopathology”

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

research A solitary triangular alopecia

April 2023 in “The Medical Journal of Australia”

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

research A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia

January 2014 in “生命科学（ISSN1934-7391）”

A certain gene variation can affect protein production and is linked to male pattern baldness.

research Caffeic acid N-[3,5-bis(trifluoromethyl)phenyl] amide as a non-steroidal inhibitor for steroid 5α-reductase type 1 using a human keratinocyte cell-based assay and molecular dynamics

December 2022 in “Scientific Reports”

Compound 4 is a promising treatment for hair loss with low toxicity.

$Synthesis and Structural Characterization of a New Dinuclear Platinum(III) Complex, [Pt2Cl4(NH3)2{μ-HN=C(O)Bu^t}2]$

research Synthesis and structural characterization of a new dinuclear platinum(III) complex, [Pt₂Cl₄(NH₃)₂{μ-HN=C(O)Bu^t}₂]

2 citations , November 2022 in “Acta crystallographica. Section B, Structural science, crystal engineering and materials./Acta crystallographica. Section B, Structural science, crystal engineering and materials”

A new platinum complex was made and studied, which might help fight cancer better.

research Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene.

78 citations , August 1996 in “The Journal of Clinical Endocrinology & Metabolism”

The same gene mutation can cause different symptoms in family members.

Unusual Systemic Lupus Erythematosus/Sjogren's Syndrome Phenotype in a Patient with a TNFAIP3 Gene Mutation

research SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION

June 2019

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

research Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5

29 citations , January 2003 in “Genomics”

A new mouse mutation causes skin and hair issues, influenced by another gene.

research Immunohistochemical expression of cytokeratin 15, cytokeratin 19, follistatin, and Bmi-1 in basal cell carcinoma

10 citations , December 2015 in “International Journal of Dermatology”

CK 15, follistatin, and Bmi-1 can help differentiate basal cell carcinoma from squamous cell carcinoma.

research Wavelength-encoded laser particles for massively-multiplexed cell tagging

10 citations , November 2018 in “bioRxiv (Cold Spring Harbor Laboratory)”

New laser particles can track thousands of cells in 3D models, improving single-cell analysis.

research AB-MTEDeep Classifier Trained with AAGAN for the Identification and Classification of Alopecia Areata

5 citations , June 2023 in “Engineering Technology & Applied Science Research”

The AI model accurately classifies Alopecia Areata with 96.94% accuracy.

Baricitinib Provides Significant Hair Regrowth in Adolescents with Severe Alopecia Areata: 52-Week Efficacy and Safety Results from a Phase 3 Randomized, Controlled Trial

research Baricitinib Provides Significant Hair Regrowth In Adolescents With Severe Alopecia Areata: 52-Week Efficacy and Safety Results From A Phase 3 Randomized, Controlled Trial

November 2025 in “SKIN The Journal of Cutaneous Medicine”

Baricitinib significantly regrows hair in teens with severe alopecia areata.

research Dermatology for the Non-Dermatologist: Triangular Alopecia

2 citations , November 1999 in “Hair transplant forum international”

The document's conclusion cannot be provided because the document is not accessible.

research Two siblings with uncombable hair syndrome: A new pathogenic variant

2 citations , March 2024 in “Pediatric Dermatology”

Two siblings have a rare hair condition caused by a new genetic variant.

research Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa

5 citations , February 2005 in “Journal of the American Academy of Dermatology”

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

research STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity

65 citations , September 2014 in “Orphanet Journal of Rare Diseases”

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

research Subjects with mild alopecia benefit from aminexil clinical 5: results of a large international observational study

1 citations , January 2020 in “IRIS UNIMORE (University of Modena and Reggio Emilia)”

Aminexil clinical 5 effectively reduces hair loss and is well-tolerated.

research Genome Report: chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus)

5 citations , August 2023 in “G3 Genes Genomes Genetics”

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

research Charting the Bromodomain BRD4: Towards the Identification of Novel Inhibitors with Molecular Similarity and Receptor Mapping

10 citations , November 2017 in “Letters in drug design & discovery”

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

Increased Retinol-Binding Protein 4 and Anti-RBP4 Antibody in Alopecia Areata

research Increased retinol‐binding protein (RBP) 4 and anti‐RBP4 antibody in alopecia areata

6 citations , June 2011 in “British Journal of Dermatology”

People with alopecia areata have higher levels of RBP4 protein and antibodies against it.

research Bioinformatics analysis and verification of m6A related genes based on the construction of keloid diagnostic model

8 citations , March 2023 in “International Wound Journal”

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

Diagnostic Value of Chromosomal Microarray Analysis in Patients With Congenital Anomalies and Dysmorphic Features; Details of Two New Patients With 2q33 Deletions

research DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS

December 2024 in “Kırıkkale Üniversitesi Tıp Fakültesi Dergisi”

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

research The Role of Box A ofHMGB1in Enhancing Stem Cell Properties of Human Mesenchymal Cells: A Novel Approach for the Pursuit of Anti-aging Therapy

1 citations , January 2023 in “In vivo/In Vivo”

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

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