VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q83287662 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241120235831.0
008 241120nneanz||abbn n and d
035 ‎‡a (WKP)Q83287662‏
024 ‎‡a 0000-0003-0537-6608‏ ‎‡2 orcid‏
024 ‎‡a 0000-0003-4624-6586‏ ‎‡2 orcid‏
024 ‎‡a 7501675082‏ ‎‡2 scopus‏
035 ‎‡a (OCoLC)Q83287662‏
100 0 ‎‡a Cheng-Rang Li‏ ‎‡c researcher (ORCID 0000-0003-0537-6608)‏ ‎‡9 en‏
400 0 ‎‡a Cheng-Rang Li‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's A case of dermatomyositis presenting with inverse Gottron's papules as the first manifestation.‏
670 ‎‡a Author's A de novo missense mutation of CYLD gene with multiple familial trichoepithelioma‏
670 ‎‡a Author's A modified method for purifying amelanotic melanocytes from human hair follicles.‏
670 ‎‡a Author's A novel missense mutation of the ATP2C1 gene in a Chinese patient with papular acantholytic dermatosis of the anogenital area.‏
670 ‎‡a Author's Acquired latent tuberculosis infection in psoriasis patients treated with etanercept in the People's Republic of China.‏
670 ‎‡a Author's Comorbidities or different entities? Phenotype variability associated with PSENEN mutations‏
670 ‎‡a Author's Hidradenitis suppurativa is treated with low-dose flutamide‏
670 ‎‡a Author's Hypermethylation of HLA-C may be an epigenetic marker in psoriasis‏
670 ‎‡a Author's Identification of a novel mutation in a Chinese patient with mild Darier's disease‏
670 ‎‡a Author's Increased serum interleukin-6 levels in patients with hidradenitis suppurativa‏
670 ‎‡a Author's Köebner Phenomenon Induced by Striae Distensae in a Vitiligo Patient.‏
670 ‎‡a Author's Linear cutaneous lupus erythematosus/discoid lupus erythematosus in an adult‏
670 ‎‡a Author's NCSTN mutations in hidradenitis suppurativa/acne inversa do not influence cytokine production by peripheral blood mononuclear cells.‏
670 ‎‡a Author's Nicastrin mutations in familial acne inversa impact keratinocyte proliferation and differentiation through the Notch and phosphoinositide 3-kinase/AKT signalling pathways‏
670 ‎‡a Author's Novel keratin 16 mutation in a Chinese family with focal palmoplantar keratoderma‏
670 ‎‡a Author's Optimization of the method for the culture of melanocyte precursors from hair follicles and their activation by 1,25-dihydroxyvitamin D3.‏
670 ‎‡a Author's Phenotype of 53 Chinese individuals with nicastrin gene mutations in association with familial hidradenitis suppurativa (acne inversa)‏
670 ‎‡a Author's Severe Darier's disease patient with mutation of ATP2A2.‏
670 ‎‡a Author's Two novel mutations of the nicastrin gene in Chinese patients with acne inversa‏
670 ‎‡a Author's Two novel nicastrin mutations in Chinese families with acne inversa‏
670 ‎‡a Author's Unilateral chromhidrosis versus unilateral pseudochromhidrosis: an interesting phenomenon.‏
909 ‎‡a (orcid) 0000000305376608‏ ‎‡9 1‏
909 ‎‡a (orcid) 0000000346246586‏ ‎‡9 1‏
909 ‎‡a (scopus) 7501675082‏ ‎‡9 1‏
919 ‎‡a caseofdermatomyositispresentingwithinversegottronspapulesasthe1manifestation‏ ‎‡A A case of dermatomyositis presenting with inverse Gottron's papules as the first manifestation.‏ ‎‡9 1‏
919 ‎‡a denovomissensemutationofcyldgenewithmultiplefamilialtrichoepithelioma‏ ‎‡A A de novo missense mutation of CYLD gene with multiple familial trichoepithelioma‏ ‎‡9 1‏
919 ‎‡a modifiedmethodforpurifyingamelanoticmelanocytesfromhumanhairfollicles‏ ‎‡A A modified method for purifying amelanotic melanocytes from human hair follicles.‏ ‎‡9 1‏
919 ‎‡a novelmissensemutationoftheatp2c1geneinachinesepatientwithpapularacantholyticdermatosisoftheanogenitalarea‏ ‎‡A A novel missense mutation of the ATP2C1 gene in a Chinese patient with papular acantholytic dermatosis of the anogenital area.‏ ‎‡9 1‏
919 ‎‡a acquiredlatenttuberculosisinfectioninpsoriasispatientstreatedwithetanerceptinthepeoplesrepublicofchina‏ ‎‡A Acquired latent tuberculosis infection in psoriasis patients treated with etanercept in the People's Republic of China.‏ ‎‡9 1‏
919 ‎‡a comorbiditiesordifferententitiesphenotypevariabilityassociatedwithpsenenmutations‏ ‎‡A Comorbidities or different entities? Phenotype variability associated with PSENEN mutations‏ ‎‡9 1‏
919 ‎‡a hidradenitissuppurativaistreatedwithlowdoseflutamide‏ ‎‡A Hidradenitis suppurativa is treated with low-dose flutamide‏ ‎‡9 1‏
919 ‎‡a hypermethylationofhla100maybeanepigeneticmarkerinpsoriasis‏ ‎‡A Hypermethylation of HLA-C may be an epigenetic marker in psoriasis‏ ‎‡9 1‏
919 ‎‡a identificationofanovelmutationinachinesepatientwithmilddariersdisease‏ ‎‡A Identification of a novel mutation in a Chinese patient with mild Darier's disease‏ ‎‡9 1‏
919 ‎‡a increasedseruminterleukin6levelsinpatientswithhidradenitissuppurativa‏ ‎‡A Increased serum interleukin-6 levels in patients with hidradenitis suppurativa‏ ‎‡9 1‏
919 ‎‡a koebnerphenomenoninducedbystriaedistensaeinavitiligopatient‏ ‎‡A Köebner Phenomenon Induced by Striae Distensae in a Vitiligo Patient.‏ ‎‡9 1‏
919 ‎‡a linearcutaneouslupuserythematosusdiscoidlupuserythematosusinanadult‏ ‎‡A Linear cutaneous lupus erythematosus/discoid lupus erythematosus in an adult‏ ‎‡9 1‏
919 ‎‡a ncstnmutationsinhidradenitissuppurativaacneinversadonotinfluencecytokineproductionbyperipheralbloodmononuclearcells‏ ‎‡A NCSTN mutations in hidradenitis suppurativa/acne inversa do not influence cytokine production by peripheral blood mononuclear cells.‏ ‎‡9 1‏
919 ‎‡a nicastrinmutationsinfamilialacneinversaimpactkeratinocyteproliferationanddifferentiationthroughthenotchandphosphoinositide3kinaseaktsignallingpathways‏ ‎‡A Nicastrin mutations in familial acne inversa impact keratinocyte proliferation and differentiation through the Notch and phosphoinositide 3-kinase/AKT signalling pathways‏ ‎‡9 1‏
919 ‎‡a novelkeratin16mutationinachinesefamilywithfocalpalmoplantarkeratoderma‏ ‎‡A Novel keratin 16 mutation in a Chinese family with focal palmoplantar keratoderma‏ ‎‡9 1‏
919 ‎‡a optimizationofthemethodforthecultureofmelanocyteprecursorsfromhairfolliclesandtheiractivationby125dihydroxyvitamind3‏ ‎‡A Optimization of the method for the culture of melanocyte precursors from hair follicles and their activation by 1,25-dihydroxyvitamin D3.‏ ‎‡9 1‏
919 ‎‡a phenotypeof53chineseindividualswithnicastringenemutationsinassociationwithfamilialhidradenitissuppurativaacneinversa‏ ‎‡A Phenotype of 53 Chinese individuals with nicastrin gene mutations in association with familial hidradenitis suppurativa (acne inversa)‏ ‎‡9 1‏
919 ‎‡a severedariersdiseasepatientwithmutationofatp2a2‏ ‎‡A Severe Darier's disease patient with mutation of ATP2A2.‏ ‎‡9 1‏
919 ‎‡a 2novelmutationsofthenicastringeneinchinesepatientswithacneinversa‏ ‎‡A Two novel mutations of the nicastrin gene in Chinese patients with acne inversa‏ ‎‡9 1‏
919 ‎‡a 2novelnicastrinmutationsinchinesefamilieswithacneinversa‏ ‎‡A Two novel nicastrin mutations in Chinese families with acne inversa‏ ‎‡9 1‏
919 ‎‡a unilateralchromhidrosisversusunilateralpseudochromhidrosisaninterestingphenomenon‏ ‎‡A Unilateral chromhidrosis versus unilateral pseudochromhidrosis: an interesting phenomenon.‏ ‎‡9 1‏
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