Výsledky vyhledávání

CAND3: a ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 11q23.1

Autor: X, Chen, L, Yang, N, Udar, T, Liang, N, Uhrhammer, S, Xu, J O, Bay, Z, Wang, S, Dandakar, S, Chiplunkar, I, Klisak, M, Telatar, H, Yang, P, Concannon, R A, Gatti

Publikováno v: Mammalian genome : official journal of the International Mammalian Genome Society. 8(2)

Using a magnetic beads-mediated cDNA selection procedure and a fetal brain expression library, we identified a transcriptional unit within a cosmid positive for the marker D11S384. Pursuit of its full-length cDNA led to the cloning of the third candi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ae91846c8de5a7849fe6c3471e545ab0
https://pubmed.ncbi.nlm.nih.gov/9060412

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Interstitial insertion of varying amounts of ABL-containing genetic material into chromosome 22 in Ph-negative CML

Autor: F, Rassool, P, Martiat, A, Taj, I, Klisak, J, Goldman

Publikováno v: Leukemia. 4(4)

We studied the cells from three selected patients with Ph-chromosome-negative chronic myeloid leukemia (CML) by Southern blotting, polymerase chain reaction, and in situ hybridization of informative probes to metaphase chromosomes. All three patients

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::018899de53e0df7874dbe0a4da3f17c9
https://pubmed.ncbi.nlm.nih.gov/2164119

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Subject Index Vol. 64, 1993

Autor: C. Collet, H. Jaafar, G.P. Chrousos, B.L. Weber, G. Levan, C. Bernabéu, M.F.G.B. Gebbink, O. Gabriel-Robez, G. Thomas, E. Petit, A.J. Solari, N. Andayani, W.H. Moolenaar, S. St-Jacques, G.A. Rouleau, C.A. Griffin, D. Olde Weghuis, K. Patel, N. Niikawa, R.F. Suijkerbuijk, B.-H. Shieh, K. Klinga Levan, H. Lewalski, C. Lee, K.J. Abel, I. Klisak, B.L. De Stavola, N.C. Vamvakopoulos, Dennis Drayna, E. Wang Jabs, J.-Y. Zhou, A.L. Hawkins, T. Kajii, R.M. Alfano, R. Wassmuth, B.O. Bengtsson, C.A. Redi, M.G. Pallavicini, D. McElligott, Robin J. Leach, M. Letarte, O. Delattre, J. Xu, Stephen Wood, T. Kishino, David Schlessinger, S.C. Chandrasekharappa, M.R. Harrison, G.R. Sutherland, M. Yerle, A. Kuwano, H. Hayes, A.D. Thompson, T. Tamura, T. Miyauchi, T. Taguchi, I. Mísek, H.-S. Hong, T.A. Jones, Jean-Louis Mandel, A. Geurts van Kessel, M.I. Pigozzi, H. Soejima, D.E. Iles, K. Yoshiura, R.B. Gaynor, R.S. Sparkes, D.J. Gilbert, F.M. Kiely, Y. Jinno, M. Giovannini, J.R. Testa, J. Zima, Y. Matsuda, J.C. Mulley, F.J. Otto, M.J. Reitsma, J.M. Shipley, Y. Lahbib-Mansais, M. Watkins, P.N. Tsichlis, T. Ohta, Y. Rumpler, M. Kawalika, L. Selleri, S. Garagna, S. Demczuk, T.W. Glover, Wl. Flejter, C.H.M. Mellink, V. Najfeld, G. Viale, E.A. Fon, T. Kaname, F.S. Collins, T. Kranert, L.M. McKenzie, A. Bellacosa, D. Muhleman, A. Swaroop, B. Wieringa, R. Suikerbuijk, P. Popescu, D. Sheer, D.E. Comings, B. Segers, J. Menninger, M. Djabali, C. Bouniol, D.W. Cooper, H.A. Phillips, S.L. Gupta, T. Bellón, N.G. Copeland, N.A. Jenkins, T. Muramatsu, A.J. Lusis, H.M. Kozman, G.A. Evans, P. Doi, E. Fernández-Ruiz, P.A. Lazo, E. Capanna, M. Macholán, H. Burda, Huntington F. Willard, J. Gellin

Publikováno v: Cytogenetic and Genome Research. 64:296-296

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fe8edadfbdb51806ece8bcf75b3e3d29
https://doi.org/10.1159/000133597

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Structural organization and DNA methylation patterning within the mouse L1 family

Autor: M E Tolberg, S S Smith, S J Funderburk, I Klisak

Publikováno v: Journal of Biological Chemistry. 262:11167-11175

We have studied stable differences in patterns of DNA methylation seen in the repeated sequences of mouse cells. A cloned 1330-base pair fragment of mouse repetitive DNA (pFS-13) was used as a probe in Southern blotting experiments. Mouse spleen and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::08488714030558bf50bf5fc1909d3d43
https://doi.org/10.1016/s0021-9258(18)60940-8

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Pentasomy X: Report of patient and studies of X-inactivation

Autor: S. J. Funderburk, M. Valente, I. Klisak, John M. Opitz

Publikováno v: American Journal of Medical Genetics. 8:27-33

A five-year-old girl presented with mental retardation (MR), microcephaly, short stature, ptosis, malocclusion, abnormal elbows, fifth finger clinodactyly, joint hyperextensibility in hands and feet, renal hypoplasia, nonobstructive ureteral stasis,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70ddf93055ea4e70c62090205bf85be8
https://doi.org/10.1002/ajmg.1320080105

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CML-T1: a cell line derived from T-lymphocyte acute phase of chronic myelogenous leukemia

Autor: RS Sparkes, K Whelan, S Ikeda, Gale Rp, M Tomonaga, I Klisak, Kazutaka Kuriyama, Michito Ichimaru, Yao E, H Yakir

Publikováno v: Blood. 74:1381-1387

Most data suggest that malignant transformation in chronic myelogenous leukemia (CML) occurs in hematopoietic stem cell that is the progenitor of myelopoiesis and of B but not T lymphopoiesis. We established a T- lymphoid cell line (CML-T1) from a pe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::162e57c58d1e5182230f038efffe3a57
https://doi.org/10.1182/blood.v74.4.1381.bloodjournal7441381

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Extended evaluation of previously reported twins with a ring 14 chromosome

Autor: R S, Sparkes, I, Klisak, M C, Sparkes

Publikováno v: Annales de genetique. 20(4)

Extended studies of recently described twins with ring(14) are presented. A single C band and nucleolar organizer region were observed in the r(14). Gene marker evaluations are compatible with monozygosity of the twins.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::133879fa590742ef569a0a0faad3c6da
https://pubmed.ncbi.nlm.nih.gov/305756

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Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2

Autor: D J, Barrett, J B, Bateman, R S, Sparkes, T, Mohandas, I, Klisak, G, Inana

Publikováno v: Investigative ophthalmologyvisual science. 28(7)

Gyrate atrophy is a hereditary chorioretinal degeneration associated with a deficiency of ornithine aminotransferase (OAT). By means of a complementary DNA clone encoding human OAT, the OAT gene sequences were mapped by somatic cell hybrids and in si

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2e7e27d1b95551479a38bab0f2c0b3c7
https://pubmed.ncbi.nlm.nih.gov/3596985

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C-band polymorphism: comparison between trisomy 21 cases and mentally retarded controls

Autor: S J, Funderburk, I, Klisak, R S, Sparkes, J, Westlake

Publikováno v: American journal of medical genetics. 5(3)

C-banding was done prospectively on 50 Down syndrome (trisomy 21) cases and 50 mentally retarded controls. Heterochromatin was quantitated by measuring the lengths of heterochromatin blocks and comparing these segments to the length of the short arm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b6c0eb835e62b58067182f11f7043866
https://pubmed.ncbi.nlm.nih.gov/6447457

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