Search
Leader | 00000nz a2200037n 45 0 | ||
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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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