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Adalimumab Improves Health-Related Quality of Life in Patients with Moderate to Severe Hidradenitis Suppurativa: Results from the First 12 Weeks of PIONEER II

research Adalimumab improves health-related quality of life (HRQoL) in patients with moderate to severe hidradenitis suppurativa (HS): Results from the first 12 weeks of PIONEER II

3 citations , May 2015 in “Journal of The American Academy of Dermatology”

Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

research Hepatocyte growth factor-modified hair follicle stem cells ameliorate cerebral ischemia/reperfusion injury in rats

12 citations , February 2023 in “Stem Cell Research & Therapy”

HGF-modified hair follicle stem cells help brain recovery after injury in rats.

research The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein

1 citations , July 2007 in “Journal of Investigative Dermatology”

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Direct Implantation of Hair-Follicle-Associated Pluripotent Stem Cells Repairs Intracerebral Hemorrhage and Reduces Neuroinflammation in Mouse Model

research Direct implantation of hair-follicle-associated pluripotent (HAP) stem cells repairs intracerebral hemorrhage and reduces neuroinflammation in mouse model

3 citations , January 2023 in “PloS one”

Implanting hair-follicle stem cells in mice brains helped repair brain bleeding and reduced brain inflammation.

research Hypertrichosis lanuginosa acquisita associated with autoimmune hepatitis

4 citations , August 2006 in “The Journal of Dermatology”

HLA can be linked to autoimmune hepatitis.

research The ultrastructure of the interfollicular epidermis of the hairless (hr/hr) mouse

23 citations , December 1977 in “Virchows Archiv B Cell Pathology”

research Skin equivalent containing collagen-human hair keratin matrice for formation of neodermis

January 2003 in “Jiepouxue zazhi”

HHK can help restore skin structure.

research CD8-positive Lymphocytes in Graft-Versus-Host Disease of Humanized NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ Mice

7 citations , February 2015 in “Journal of comparative pathology”

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

research Severe Variant of X‐linked Dyskeratosis Congenita (Hoyeraal‐Hreidarsson Syndrome) Causes Significant Enterocolitis in Early Infancy

26 citations , August 2009 in “Journal of Pediatric Gastroenterology and Nutrition”

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

research S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis

October 2020 in “The American Journal of Gastroenterology”

Early diagnosis and treatment of hereditary hemochromatosis can prevent serious complications.

research An endocrinopathy characterized by dysfunction of the pituitary-adrenal axis and alopecia universalis: supporting the entity of a triple H syndrome

1 citations , September 2002 in “European Journal of Endocrinology”

Triple H syndrome exists and can vary in symptoms.

research The accelerated aging skin in rhino‐like SHJH^hr mice

1 citations , June 2022 in “Experimental dermatology”

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

research 51223 A novel human disease model of alopecia areata to evaluate benefit of the DHODH inhibitor farudodstat

1 citations , September 2024 in “Journal of the American Academy of Dermatology”

Farudodstat may effectively treat alopecia areata without harmful side effects.

research Design and initial characterization of fabricated composite scaffold dHPCTM-HPE (decellularized human placental connective tissue matrix - human placental extract)

October 2023 in “Research Square (Research Square)”

The new composite scaffold may effectively treat chronic and deep wounds.

research Hairless Modulates Ligand-Dependent Activation of the Vitamin D Receptor-Retinoid X Receptor Heterodimer

28 citations , January 2012 in “Biological & pharmaceutical bulletin”

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

research Defective control of growth rate and cell diameter in tip-growing root hairs of therhd4mutant ofArabidopsis thaliana

26 citations , September 1999 in “Canadian Journal of Botany”

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

research The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes

35 citations , April 2008 in “Journal of Biological Chemistry”

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

research Preoperative Ultrasound for Evaluation of Hidradenitis Suppurativa

2 citations , January 2019 in “Dermatologic Surgery”

research O potencial de cicatrização do hidrogel Qui/HPMC/Ins

November 2024

research Seventy‐MHz Ultrasound Detection of Early Signs Linked to the Severity, Patterns of Keratin Fragmentation, and Mechanisms of Generation of Collections and Tunnels in Hidradenitis Suppurativa

41 citations , November 2019 in “Journal of Ultrasound in Medicine”

Ultrasound can help detect early signs and severity of hidradenitis suppurativa.

research A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia

37 citations , October 2006 in “Archives of Biochemistry and Biophysics”

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

research Platelet-Rich Plasma Hybridized Adipose Transplant (PHAT) for the Treatment of Hair Loss

January 2022 in “Aesthetic Plastic Surgery”

research Hair Follicle Pluripotent Stem (hfPS) Cells

2 citations , January 2009 in “Human cell culture”

Risk Factors, Prevalence, and Diagnosis of Hutchinson-Gilford Syndrome with Special Reference to Case Reports

research RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS

2 citations , May 2017 in “International journal of pharmacy and pharmaceutical sciences/International Journal of Pharmacy and Pharmaceutical Sciences”

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

research Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».

January 2008 in “HAL (Le Centre pour la Communication Scientifique Directe)”

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

research Expression of 11β-hydroxysteroid dehydrogenase type 1 in visceral and subcutaneous adipose tissues of patients with polycystic ovary syndrome is associated with adiposity

18 citations , December 2010 in “The Journal of Steroid Biochemistry and Molecular Biology”

Increased HSD11B1 enzyme expression is linked to higher body fat and insulin resistance.

Hereditary Vitamin D Resistant Rickets (HVDRR) Case Series: Phenotype, Genotype, Conventional Treatment, and Adjunctive Cinacalcet Therapy

research Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy

1 citations , January 2024 in “Pediatric Endocrinology Diabetes and Metabolism”

Cinacalcet may help treat hereditary vitamin D resistant rickets safely.

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