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Aberrant expression of IL-22 receptor 1 and autocrine IL-22 stimulation contribute to tumorigenicity in ALK+ anaplastic large cell lymphomaDIEN BARD, J; GELEBART, P; ANAND, M et al.Leukemia. 2008, Vol 22, Num 8, pp 1595-1603, issn 0887-6924, 9 p.Article

Prenatal diagnosis of jumping translocation involving chromosome 22 with ultrasonographic findingsASLAN, Halil; KARAMAN, Birsen; YILDIRIM, Gokhan et al.Prenatal diagnosis. 2005, Vol 25, Num 11, pp 1024-1027, issn 0197-3851, 4 p.Article

OnpA, an Unusual Flavin-Dependent Monooxygenase Containing a Cytochrome b5 DomainYI XIAO; LIU, Ting-Ting; HUI DAI et al.Journal of bacteriology. 2012, Vol 194, Num 6, pp 1342-1349, issn 0021-9193, 8 p.Article

Cytogenetic heterogeneity in blast crisis (BC) of chronic myelogenous leukemia (CML)ABRAMSON, J; VERMA, R. S; SCHWARTZ, J et al.Blut. 1985, Vol 51, Num 5, pp 361-363, issn 0006-5242Article

"CRI DU CHAT" SYNDROME DUE TO A COMPLEX REARRANGEMENT OF CHROMOSOME 5FRANCESCONI D; ZUFFARDI O; D'ATTOMA G et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 2; PP. 113-115; ABS. FRE; BIBL. 8 REF.Article

BRIEF COMMUNICATION: SPECIFICITY OF THE 5 Q-CHROMOSOME IN A DISTINCT TYPE OF REFRACTORY ANEMIA.VERHEST A; VAN SCHOUBROECK F; WITTEK M et al.1976; J. NATION. CANCER INST.; U.S.A.; DA. 1976; VOL. 56; NO 5; PP. 1053-1054; BIBL. 8 REF.Article

RING CHROMOSOME 5 IN TWO MALFORMED BOYS WITH CRI DU CHAT SYNDROMESUERINCK E; NOEL B; RETHORE MO et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 3; PP. 125-129; BIBL. 5 REF.Article

A PROPOS D'UNE OBSERVATION DE MALADIE DU CRI DU CHAT.CASTEL Y; TOUDIC L; RIVIERE D et al.1977; REV. INTERNATION. PEDIATR.; FR.; DA. 1977; NO 76; PP. 29-42; BIBL. 19 REF.Article

Assignment1 of ankyrin repeat, family A (RFXANK-like) 2 (ANKRA2) to human chromosome 5q12→q13 by radiation hybrid mapping and somatic cell hybrid PCRRADER, K; BOYER, A. D; FARQUHAR, M. G et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 3-4, pp 164-165, issn 0301-0171Article

International workshop on human chromosome 5 mapping 1992Cytogenetics and cell genetics. 1992, Vol 61, Num 4, pp 225-242, issn 0301-0171Conference Proceedings

DELETION OF THE SHORT ARM OF CHROMOSOME 5 FROM A SUBJECT WITH CRI-DU-CHAT SYNDROME. REPOSITORY IDENTIFICATION NO. GM71.BREG WR; ARONSON MM; GREENE AE et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 4; PP. 239-240; BIBL. 3 REF.Article

Covalent cross-linking of the active sites of vesicle-bound cytochrome b5 and NADH-cytochrome b5 reductaseHACKETT, C. S; STRITTMATTER, P.The Journal of biological chemistry (Print). 1984, Vol 259, Num 5, pp 3275-3282, issn 0021-9258Article

An anonymous DNA segment pTP5E (D5S70) maps to the long arm of chromosome 5 and identifies a Taq I polymorphismFARBER, R. A; PHALEN, T; NEUMAN, W. L et al.Nucleic acids research. 1988, Vol 16, Num 5, issn 0305-1048, 2360, part BArticle

Unusual dehydroxylation of antimicrobial amidoxime prodrugs by cytochrome b5 and nadh cytochrome b5 reductaseSAULTER, Janelle Y; KURIAN, Joseph R; TREPANIER, Lauren A et al.Drug metabolism and disposition. 2005, Vol 33, Num 12, pp 1886-1893, issn 0090-9556, 8 p.Article

Cytochrome b5 and NADH cytochrome b5 reductase: genotype-phenotype correlations for hydroxylamine reductionSACCO, James C; TREPANIER, Lauren A.Pharmacogenetics and genomics (Print). 2010, Vol 20, Num 1, pp 26-37, issn 1744-6872, 12 p.Article

5q-syndrome: complete response to chemotherapyCONNEALLY, E; SHERRINGTON, P; FISCHER, P et al.Clinical and laboratory haematology. 1990, Vol 12, Num 1, pp 101-103, issn 0141-9854, 3 p.Article

Stimulation and clustering of cytochrome b5 reductase in caveolin-rich lipid microdomains is an early event in oxidative stress-mediated apoptosis of cerebellar granule neuronsSAMHAN-ARIAS, Alejandro K; MARQUES-DA-SILVA, Dorinda; YANAMALA, Naveena et al.Journal of proteomics (Print). 2012, Vol 75, Num 10, pp 2934-2949, issn 1874-3919, 16 p.Conference Paper

A CRI-DU-CHAT INFANT BORN TO A MOTHER CARRYING A 5/17 BALANCED TRANSLOCATION.KADOTANI T; HIYAMA Y; KAWAKAMI M et al.1977; PROC. JAP. ACAD.; JAP.; DA. 1977; VOL. 53; NO 3; PP. 155-158; BIBL. 10 REF.Article

PARTIAL TRISOMY FOR SHORT AND LONG ARM OF CHROMOSOME NO 5. TWO CASES OF TWO POSSIBLE SYNDROMES.ZABEL B; BAUMANN W; GEHLER J et al.1978; J. MED. GENET.; G.B.; DA. 1978; VOL. 15; NO 2; PP. 143-147; BIBL. 12 REF.Article

Topography, Clinical, and Genomic Correlates of 5q Myeloid Malignancies RevisitedJEREZ, Andres; GONDEK, Lukasz P; MCDEVITT, Michael A et al.Journal of clinical oncology. 2012, Vol 30, Num 12, pp 1343-1349, issn 0732-183X, 7 p.Article

The DNA sequence and comparative analysis of human chromosome 5SCHMUTZ, Jeremy; MARTIN, Joel; HELLSTEN, Uffe et al.Nature (London). 2004, Vol 431, Num 7006, pp 268-274, issn 0028-0836, 7 p.Article

Assignment of the ectodermal-neural cortex 1 gene (ENC1) to human chromosome band 5q13 by in situ hybridizationHERNANDEZ, M.-C; ANDRES-BARQUIN, P. J; KUO, W.-L et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 89-90, issn 0301-0171Article

Refined mapping of the GM2 activator protein (GM2A) locus to 5q31.3-q33.1, distal to the spinal muscular atrophy locusHENG, H. H. Q; BEI XIE; XIAO-MEI SHI et al.Genomics (San Diego, Calif.). 1993, Vol 18, Num 2, pp 429-431, issn 0888-7543Article

A new RFLP for L1.4 (D5S4) an anonymous genomic clone localised to chromosome 5BAILEY, C. J; RIDER, S. H; BODMER, W. F et al.Nucleic acids research. 1987, Vol 15, Num 16, issn 0305-1048, 6762Article

PRENATAL DIAGNOSIS OF 5 P.DAVID K; KAFFE S; STRAUSS L et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 2; PP. 224-228; BIBL. 12 REF.Article

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