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research Inhibition of the development of metastatic squamous cell carcinoma in protein kinase C epsilon transgenic mice by alpha-difluoromethylornithine accompanied by marked hair follicle degeneration and hair loss.

26 citations , June 2003 in “PubMed”

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

research Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion

4 citations , October 2021 in “Journal of Clinical Medicine”

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

research Monilethrix, a rare inherited hair shaft disorder in siblings

4 citations , January 2014 in “Indian dermatology online journal”

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

research 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증

January 2011 in “대한피부과학회지”

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

research Cornification in reptilian epidermis occurs through the deposition of keratin‐associated beta‐proteins (beta‐keratins) onto a scaffold of intermediate filament keratins

33 citations , October 2012 in “Journal of Morphology”

Reptile skin hardens by layering beta-proteins on keratin.

research Novel associations of VPS13C with phenotype and conversion of idiopathic REM sleep behavior disorder

April 2026 in “npj Parkinson s Disease”

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

research L-Ornithine ketoacid-transaminase assay in hair roots of homozygotes and heterozygotes for gyrate atrophy

8 citations , June 1981 in “Clinica Chimica Acta”

research Reversible severe myopathy during treatment with finasteride

15 citations , April 1997 in “Muscle & Nerve”

research Reversible severe myopathy during treatment with finasteride

5 citations , April 1997 in “Muscle & Nerve”

research Trichohyalin: Purification from Porcine Tongue Epithelium and Characterization of the Native Protein

16 citations , June 1992 in “Journal of Investigative Dermatology”

research Connexin mutations in human disease

4 citations , September 2004 in “Experimental Dermatology”

Connexin mutations can cause various diseases like hearing loss and skin disorders.

Poly(γ-Glutamic Acid)/Chitosan Hydrogel Nanoparticles for Effective Preservation and Delivery of Fermented Herbal Extract for Enlarging Hair Bulb and Enhancing Hair Growth

research
Poly(γ-Glutamic Acid)/Chitosan Hydrogel Nanoparticles For Effective Preservation And Delivery Of Fermented Herbal Extract For Enlarging Hair Bulb And Enhancing Hair Growth

22 citations , October 2019 in “International Journal of Nanomedicine”

The nanoparticles improved hair growth and enlarged hair bulbs.

research Atrichia with papular lesions

8 citations , January 2011 in “International journal of trichology”

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

research Characterizing enteric neurons in dopamine transporter (DAT)‐Cre reporter mice reveals dopaminergic subtypes with dual‐transmitter content

March 2024 in “European Journal of Neuroscience”

Dopaminergic neurons in the gut have diverse subtypes with different neurotransmitter contents.

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 Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia

1 citations , May 2011 in “DOAJ (DOAJ: Directory of Open Access Journals)”

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

research Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation

6 citations , January 2022 in “BMC Medical Genomics”

Different gene mutations cause different types of ichthyosis, with some new mutations found.

research The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep

January 2002 in “Agritrop (Cirad)”

The hr gene is linked to hair loss in Valle del Belice sheep.

research Characterization of tiger tail banding and hair shaft abnormalities in trichothiodystrophy

7 citations , March 2004 in “Journal of the American Academy of Dermatology”

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

research Analysis of Cysteine on the Surface of Hair Fibers with Spectrofluorescence

January 2008 in “Chinese Journal of Spectroscopy Laboratory”

Cysteine formation on hair indicates damage, best detected at pH 4.5.

research 1386 Trichodysplasia spinulosa small T antigen drives ectopic hair follicle development in adult transgenic mice

1 citations , April 2018 in “Journal of Investigative Dermatology”

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

research Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles

August 2022 in “Frontiers in genetics”

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

research In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments

91 citations , December 2000 in “The journal of cell biology/The Journal of cell biology”

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.

research Concerted gene duplications in the two keratin gene families

53 citations , May 1988 in “Journal of Molecular Evolution”

research Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations

115 citations , October 2009 in “The Journal of clinical endocrinology and metabolism/Journal of clinical endocrinology & metabolism”

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

research Molecular insights into the formation of drug-polymer inclusion complex

October 2023

The research shows how certain drugs can form stable structures with polymers, which is important for making new pharmaceuticals.

research Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China

3 citations , September 2013 in “Journal of the American Academy of Dermatology”

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

research Polyamine-controlled proliferation and protein biosynthesis are independent determinants of hair follicle stem cell fate

1 citations , April 2020 in “bioRxiv (Cold Spring Harbor Laboratory)”

Polyamines are important in deciding hair follicle stem cell behavior, affecting hair growth and loss.

research Self-Assembled Peptide Hydrogels in Regenerative Medicine

August 2023 in “Gels”

Peptide hydrogels show promise for healing skin, bone, and nerves but need improvement in stability and compatibility.

Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs

research Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs

28 citations , February 2012 in “PLoS ONE”

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

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