Zobrazeno 1 - 10
of 36
pro vyhledávání: '"O, Lustig"'
Autor:
Joan Slight, Nicholas D. Hastie, Tatiana Dudnakova, J Cotterell, Lee Spraggon, Colin G. Miles, O Lustig-Yariv
Publikováno v:
Oncogene. 26:1484-1491
The Wilms' tumour suppressor gene, WT1, encodes a zinc-finger protein that is mutated in Wilms' tumours and highly expressed in a wide variety of other malignancies. WT1 is a transcription factor that is likely to have additional, post-transcriptiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93f71db4927346d0d9085f91c26d9385
https://doi.org/10.1038/sj.onc.1209922
https://doi.org/10.1038/sj.onc.1209922
Autor:
O. Lustig, Edward E. Wallach, Zion Ben-Rafael, Nathan de-Groot, Abraham Hochberg, Ran Goshen, Bernard Gonik, Vasilios Tannos
Publikováno v:
Fertility and Sterility. 62:903-910
Objectives To outline the possible role of the imprinted genes in early human embryogenesis and implantation. Data Identification Literature review. Study Selection Studies examining the issues of genomic imprinting, implantation, gestational trophob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcf57b7c502500ff6cbb060b7d1c6740
https://doi.org/10.1016/s0015-0282(16)57048-4
https://doi.org/10.1016/s0015-0282(16)57048-4
Publikováno v:
Molecular Reproduction and Development. 38:239-246
The H19 gene is a parenterally imprinted maternally expressed gene which has a pivotal role in embryogenesis and fetal development. It is tightly linked to the IGF-II gene on chromosome 11p15.5 which is reciprocally imprinted. We studied the expressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ceb5292e235536285c718983a526c60
https://doi.org/10.1002/mrd.1080380302
https://doi.org/10.1002/mrd.1080380302
Publikováno v:
Placenta. 15:285-302
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14f029a427cdc9fbb84535cd402d437c
https://doi.org/10.1016/s0143-4004(05)80352-2
https://doi.org/10.1016/s0143-4004(05)80352-2
Autor:
O Lustig-Yariv, Avraham Hochberg, E Schulze, Volker A. Erdmann, Dymitr Komitowski, T Schneider, N. de Groot
Publikováno v:
Oncogene. 15(2)
H19 is a paternally imprinted gene with unknown function. It is located in close proximity to the maternally imprinted IGF-2 gene on chromosome 11p15.5. In this study no consistent relationship between the expression of these two genes in clones deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc308adcb005c48136018d1b0c4f8161
https://pubmed.ncbi.nlm.nih.gov/9244352
https://pubmed.ncbi.nlm.nih.gov/9244352
Autor:
J, Rachmilewitz, M, Elkin, L H, Looijenga, A J, Verkerk, B, Gonik, O, Lustig, D, Werner, N, de Groot, A, Hochberg
Publikováno v:
Oncogene. 13(8)
IPW (Imprinted gene in the Prader-Willi syndrome region) is a recently identified paternally expressed gene. Previous work has demonstrated IPW expression in the human fetus and adult, with monoallelic expression in adult lymphoblasts and fibroblasts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fff827dd62e29ed99a1bbd85c07b8f84
https://pubmed.ncbi.nlm.nih.gov/8895514
https://pubmed.ncbi.nlm.nih.gov/8895514
Autor:
R, Goshen, I, Ariel, D, Komitowski, O, Lustig-Yariv, D, Pode, G, Pizov, N, De Groot, A, Hochberg
Publikováno v:
Harefuah. 129(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e0a7f3742cffaf301dbaf8c757ac4ef2
https://pubmed.ncbi.nlm.nih.gov/8549984
https://pubmed.ncbi.nlm.nih.gov/8549984
Autor:
J, Rachmilewitz, M, Elkin, J, Rosensaft, Z, Gelman-Kohan, I, Ariel, O, Lustig, T, Schneider, R, Goshen, H, Biran, N, de Groot
Publikováno v:
Oncogene. 11(5)
Certain embryonal tumors demonstrate a loss of heterozygosity at the parentally imprinted region of chromosome 11p15.5. It has been hypothesized that this implicates a tumor suppressor gene at this locus. The human H19 gene maps to 11p15.5, is expres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4ce01171d42982ff10efb37148e3709d
https://pubmed.ncbi.nlm.nih.gov/7545806
https://pubmed.ncbi.nlm.nih.gov/7545806
Autor:
Abraham Hochberg, Mally Sappir, O. Lustig, Tamar Schneider, Ilana Ariel, Galina Pizov, Nathan de-Groot
Publikováno v:
Urology. 45(2)
Objectives. Genomic imprinting is a newly discovered mechanism in genetics that is involved in tumorigenesis. H19 is an imprinted gene in the human, expressed from the maternal allele. It is extensively transcribed in fetal life but is not translated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1faee2fe715a8f98e8072d089ba99044
https://pubmed.ncbi.nlm.nih.gov/7855987
https://pubmed.ncbi.nlm.nih.gov/7855987
Autor:
Bernard Gonik, Avraham Hochberg, Michael Elkin, Jacob Rachmilewitz, C.E. Oyer, N. de Groot, Ran Goshen, H. Biran, I Ariel, O. Lustig
Publikováno v:
Gynecologic oncology. 53(2)
Genomic imprinting—the uniparental-dependent transmittance of a genetic trait—has been accepted in recent years as a major mechanism in mammalian genetics. We studied the expression of the H19 gene, a parentally imprinted (maternally expressed) g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52507ace43a207a0213a5a21dc43370a
https://pubmed.ncbi.nlm.nih.gov/8188082
https://pubmed.ncbi.nlm.nih.gov/8188082