Genomic imprinting: a possible mechanism for the parental origin effect of Huntington's choreaREIK, W.Journal of medical genetics. 1988, Vol 25, Num 12, pp 805-808, issn 0022-2593Article

Höherer Komfort und weniger Geräusch durch das ZweimassenschwungradREIK, W.ATZ. Automobiltechnische Zeitschrift. 1998, Vol 100, Num 12, pp 896-900, issn 0001-2785Article

Genomic imprinting in mammalsREIK, W.Results and problems in cell differentiation. 1992, Num 18, pp 203-227, issn 0080-1844Article

VERGLEICH DER WOEHLER-KURVEN AUS SPANNUNGSGESTEUERTEN, GESAMTDEHNUNGSGESTEUERTEN UND PLASTISCHDEHNUNGSGESTEUERTEN VERSUCHEN = COMPARISON OF THE S/N CURVES FROM STRESS-CONTROLLED, TOTAL-STRAIN-CONTROLLED AND PLASTIC-STRAIN-CONTROLLED TESTSREIK W; MAYR P; MACHERAUCH E et al.1979; ARCH. EISENHUETTENWES.; DEU; DA. 1979-09; VOL. 50; NO 9; PP. 407-411; BIBL. 16 REF.Article

VERGLEICH DER WOEHLER-KURVEN AUS SPANNUNGSGESTEUERTEN, GESAMTDEHNUNGSGESTEUERTEN UND PLASTISCHDEHNUNGSGESTEUERTEN VERSUCHEN = COMPARISON OF THE S/N CURVES FROM STRESS-CONTROLLED, TOTAL-STRAIN-CONTROLLED AND PLASTIC-STRAIN-CONTROLLED TESTSREIK W; MAYR P; MACHERAUCH E et al.1979; ARCH. EISENHUETTENWES.; DEU; DA. 1979-09; VOL. 50; NO 9; PP. 407-411; BIBL. 16 REF.Article

MAKROSKOPISCHE LAENGENAENDERUNGEN ALS FOLGE VON MITTELSPANNUNGSWECHSELN BEI ZUG-DRUCK-WECHSELVERFORMUNG VON CK 45 = MACROSCOPIC CHANGES OF LENGTH AS A CONSEQUENCE OF CHANGES OF MEAN STRESS DURING CYCLIC TENSION-COMPRESSION TESTS OF CK 45PILO D; REIK W; MAYR P et al.1979; ARCH. EISENHUETTENWES.; DEU; DA. 1979-10; VOL. 50; NO 10; PP. 439-442; BIBL. 6 REF.Article

INHOMOGENE DEFORMATIONSVORGAENGE IN DER ANRISSFREIEN ERDMUEDUNGSPHASE UNLEGIERTER STAEHLE. = PHENOMENES DE DEFORMATION HETEROGENE DANS DES ACIERS AU CARBONE AU COURS DE LA PHASE INITIALE, EXEMPTE DE FISSURATIONS D'UN ESSAI DE FATIGUEPILO D; REIK W; MAYR P et al.1977; ARCH. EISENHUETTENWES.; DTSCH.; DA. 1977; VOL. 48; NO 11; PP. 575-578; ABS. ANGL. FR.; BIBL. 12 REF.Article

Retrovirus integration and chromatin structure: Moloney murine leukemia proviral integration sites map near DNase I-hypersensitive sitesROHDEWOHLD, H; WEIHER, H; REIK, W et al.Journal of virology. 1987, Vol 61, Num 2, pp 336-343, issn 0022-538XArticle

CpG methylation of an X-linked transgene is determined by somatic events postfertilization and not germline imprintingCOLLICK, A; REIK, W; BARTON, S. C et al.Development (Cambridge). 1988, Vol 104, Num 2, pp 235-244Article

Methylation analysis on individual chromosomes : improved protocol for bisulphite genomic sequencingFEIL, R; CHARLTON, J; BIRD, A. P et al.Nucleic acids research. 1994, Vol 22, Num 4, pp 695-696, issn 0305-1048Article

Systematic elimination of parthenogenetic cells in mouse chimerasFUNDELE, R; NORRIS, M. L; BARTON, S. C et al.Development (Cambridge). 1989, Vol 106, Num 1, pp 29-35Article

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndromeSUN, F.-L; DEAN, W. L; KELSEY, G et al.Nature (London). 1997, Vol 389, Num 6653, pp 809-815, issn 0028-0836Article

Genomic imprinting determines methylation of parental alleles in transgenic miceREIK, W; COLLICK, A; NORRIS, M. L et al.Nature (London). 1987, Vol 328, Num 6127, pp 248-251, issn 0028-0836Article

Provision of the immunoglobulin heavy chain enhancer downstream of a test gene is sufficient to confer lymphoid-specific expression in transgenic miceREIK, W; WILLIAMS, G; BARTON, S et al.European journal of immunology. 1987, Vol 17, Num 4, pp 465-469, issn 0014-2980Article

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domainREIK, W; BROWN, K. W; SCHNEID, H et al.Human molecular genetics (Print). 1995, Vol 4, Num 12, pp 2379-2385, issn 0964-6906Article

Parental impriming: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) geneSASAKI, H; JONES, P. A; CHAILLET, J. R et al.Genes & development. 1992, Vol 6, Num 10, pp 1843-1856, issn 0890-9369Article

Transgenes as probes for active chromosomal domains in mouse developmentALLEN, N. D; CRAN, D. G; BARTON, S. C et al.Nature (London). 1988, Vol 333, Num 6176, pp 852-855, issn 0028-0836Article

Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndromeREIK, W; BROWN, K. W; SLATTER, R. E et al.Human molecular genetics (Print). 1994, Vol 3, Num 8, pp 1297-1301, issn 0964-6906Article

Developmental consequences of imprinting of parental chromosomes by DNA methylationSURANI, M. A; ALLEN, N. D; BARTON, S. C et al.Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 1990, Vol 326, Num 1235, pp 313-327, issn 0080-4622, 15 p., [16 p]Conference Paper

Imprinting of IGF2 and H19 : lack of reciprocity in sporadic Beckwith-Wiedemann syndromeJOYCE, J. A; LAM, W. K; CATCHPOOLE, D. J et al.Human molecular genetics (Print). 1997, Vol 6, Num 9, pp 1543-1548, issn 0964-6906Article

Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mousePAULSEN, M; EL-MAARRI, O; ENGEMANN, S et al.Human molecular genetics (Print). 2000, Vol 9, Num 12, pp 1829-1841, issn 0964-6906Article

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathwayBROWN, K. W; VILLAR, A. J; BICKMORE, W et al.Human molecular genetics (Print). 1996, Vol 5, Num 12, pp 2027-2032, issn 0964-6906Article

Adult phenotype in the mouse can be affected by epigenetic events in the early embryoREIK, W; RÖMER, I; BARTON, S. C et al.Development (Cambridge). 1993, Vol 119, Num 3, pp 933-942, issn 0950-1991Article

Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and humanMONK, D; SANCHES, R; CONSTANCIA, M et al.Human molecular genetics (Print). 2006, Vol 15, Num 8, pp 1259-1269, issn 0964-6906, 11 p.Article

Silencing of cdknic (p57^KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndromeDIAZ-MEYER, N; DAY, C. D; HIGGINS, M. J et al.Journal of medical genetics. 2003, Vol 40, Num 11, pp 797-801, issn 0022-2593, 5 p.Article