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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

Schwingungsverhalten eines Pkw-Antriebsstranges mit Zweimassenschwungrad = Comportement vibratoire d'une transmission d'automobile comprenant un volant d'inertie à deux masses = Vibration behaviour of a passenger car transmission with a two-weights flywheelREIK, W.VDI-Berichte. 1988, Num 697, pp 173-194, issn 0083-5560Conference Paper

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

Methylation levels of maternal and paternal genomes during preimplantation developmentHOWLETT, S. K; REIK, W.Development (Cambridge). 1991, Vol 113, Num 1, pp 119-127, issn 0950-1991Article

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

ZUM MITTELSPANNUNGSEINFLUSS AUF DAS WECHSELVERFORMUNGSVERHALTEN UNLETIERTER STAEHLE. = INFLUENCE DE LA CONTRAINTE MOYENNE SUR LE COMPORTEMENT A LA FATIGUE D'ACIERS NON ALLIESPILO D; REIK W; MAYR P et al.1978; ARCH. EISENHUETTENWES.; DTSCH.; DA. 1978; VOL. 49; NO 1; PP. 31-36; ABS. ANGL. FR.; BIBL. 6 REF.Article

Imprinting in clusters : lessons from Beckwith-Wiedemann syndromeREIK, W; MAHER, E. R.Trends in genetics (Regular ed.). 1997, Vol 13, Num 8, pp 330-334, issn 0168-9525Article

Development control of allelic methylation in the imprinted mouse lgf2 and H19 genesFEIL, R; WALTER, J; ALLEN, N. D et al.Development (Cambridge). 1994, Vol 120, Num 10, pp 2933-2943, issn 0950-1991Article

Imprinting by DNA methylation : from transgenes to endogenous gene sequencesREIK, W; HOWLETT, S. K; SURANI, M. A et al.Development (Cambridge). 1990, pp 99-106, issn 0950-1991, 8 p., SUPConference Paper

Replication-competent Moloney murine leukemia virus carrying a bacterial suppressor tRNA gene: selective cloning of proviral and flanking host sequencesREIK, W; WEIHER, H; JAENISCH, R et al.Proceedings of the National Academy of Sciences of the United States of America. 1985, Vol 82, Num 4, pp 1141-1145, issn 0027-8424Article

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

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

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

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

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

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

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

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

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