VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q57235347 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241120235808.0
008 241120nneanz||abbn n and d
035 ‎‡a (WKP)Q57235347‏
024 ‎‡a 0000-0002-2283-3690‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q57235347‏
100 0 ‎‡a ستيفان ماير‏ ‎‡9 ar‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a Stefan Meyer‏ ‎‡9 es‏ ‎‡9 ast‏
400 0 ‎‡a Stefan Meyer‏ ‎‡c researcher (ORCID 0000-0002-2283-3690)‏ ‎‡9 en‏
400 0 ‎‡a Stefan Meyer‏ ‎‡c onderzoeker‏ ‎‡9 nl‏
670 ‎‡a Author's Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption.‏
670 ‎‡a Author's Correction to: Infantile fibrosarcoma with TPN3-NTRK3 fusion in a boy with Bloom Syndrome‏
670 ‎‡a Author's EVI1 oncoprotein expression and CtBP1-association oscillate through the cell cycle‏
670 ‎‡a Author's EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewal‏
670 ‎‡a Author's Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling‏
670 ‎‡a Author's Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.‏
670 ‎‡a Author's Genomic profiling of acute myeloid leukaemia associated with ataxia telangiectasia identifies a complex karyotype with wild-type TP53 and mutant KRAS, G3BP1 and IL7R‏
670 ‎‡a Author's Human TRIB2 Oscillates during the Cell Cycle and Promotes Ubiquitination and Degradation of CDC25C‏
670 ‎‡a Author's Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome‏
670 ‎‡a Author's Patterns and frequency of renal abnormalities in Fanconi anaemia: implications for long-term management.‏
670 ‎‡a Author's Phosphorylation of the leukemic oncoprotein EVI1 on serine 196 modulates DNA binding, transcriptional repression and transforming ability‏
909 ‎‡a (orcid) 0000000222833690‏ ‎‡9 1‏
919 ‎‡a fanconianemiawithsunsensitivitycausedbyaxerodermapigmentosumassociatedmissensemutationinxpf‏ ‎‡A Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.‏ ‎‡9 1‏
919 ‎‡a humantrib2oscillatesduringthecellcycleandpromotesubiquitinationanddegradationofcdc25c‏ ‎‡A Human TRIB2 Oscillates during the Cell Cycle and Promotes Ubiquitination and Degradation of CDC25C‏ ‎‡9 1‏
919 ‎‡a infantilefibrosarcomawithtpm3ntrk1fusioninaboywithbloomsyndrome‏ ‎‡A Infantile fibrosarcoma with TPM3-NTRK1 fusion in a boy with Bloom syndrome‏ ‎‡9 1‏
919 ‎‡a patternsandfrequencyofrenalabnormalitiesinfanconianaemiaimplicationsforlongtermmanagement‏ ‎‡A Patterns and frequency of renal abnormalities in Fanconi anaemia: implications for long-term management.‏ ‎‡9 1‏
919 ‎‡a phosphorylationoftheleukemiconcoproteinevi1onserine196modulatesdnabindingtranscriptionalrepressionandtransformingability‏ ‎‡A Phosphorylation of the leukemic oncoprotein EVI1 on serine 196 modulates DNA binding, transcriptional repression and transforming ability‏ ‎‡9 1‏
919 ‎‡a genomicprofilingofacutemyeloidleukaemiaassociatedwithataxiatelangiectasiaidentifiesacomplexkaryotypewithwildtypetp53andmutantkrasg3bp1andil7r‏ ‎‡A Genomic profiling of acute myeloid leukaemia associated with ataxia telangiectasia identifies a complex karyotype with wild-type TP53 and mutant KRAS, G3BP1 and IL7R‏ ‎‡9 1‏
919 ‎‡a fanconianaemiabrca2mutationsandchildhoodcanceradevelopmentalperspectivefromclinicalandepidemiologicalobservationswithimplicationsforgeneticcounselling‏ ‎‡A Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling‏ ‎‡9 1‏
919 ‎‡a evi1phosphorylationats436regulatesinteractionswithctbp1anddnmt3aandpromotesselfrenewal‏ ‎‡A EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewal‏ ‎‡9 1‏
919 ‎‡a evi1oncoproteinexpressionandctbp1associationoscillatethroughthecellcycle‏ ‎‡A EVI1 oncoprotein expression and CtBP1-association oscillate through the cell cycle‏ ‎‡9 1‏
919 ‎‡a correctiontoinfantilefibrosarcomawithtpn3ntrk3fusioninaboywithbloomsyndrome‏ ‎‡A Correction to: Infantile fibrosarcoma with TPN3-NTRK3 fusion in a boy with Bloom Syndrome‏ ‎‡9 1‏
919 ‎‡a acquiredcrosslinkerresistanceassociatedwithanovelsplicedbrca2proteinvariantformolecularphenotypingofbrca2disruption‏ ‎‡A Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption.‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
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996 ‎‡2 LC|no 96064214
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏