Zobrazeno 1 - 10
of 178
pro vyhledávání: '"Milatovich, A."'
Autor:
P J Cornbleet, Carol D. Jones, James L. Zehnder, Yasodha Natkunam, Roger A. Warnke, Athena Milatovich-Cherry
Publikováno v:
The American Journal of Surgical Pathology. 24:525-534
Progression of follicular lymphoma to a higher-grade malignancy frequently heralds a poor prognosis. Clinical transformation is variably accompanied by a spectrum of histologic changes characterized by alteration in growth and cytology. Although seve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fc76a4cf0b2f7004cada47f1569dff1
https://doi.org/10.1097/00000478-200004000-00006
https://doi.org/10.1097/00000478-200004000-00006
Autor:
Johannes G. Dauwerse, Lester Weiss, Howard M. Saal, Fred Petrij, Ruthann I. Blough, Jack H. Rubinstein, Athena Milatovich-Cherry
Publikováno v:
American Journal of Medical Genetics. 90:29-34
Most reported microdeletions of the CREB-binding protein (CBP) gene in the Rubinstein-Taybi syndrome (RTS) were detected by fluorescence in situ hybridization (FISH) with a single cosmid probe specific to the 3' region of the gene. In order to test t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c17c13220069a973165a247ed8b619fe
https://doi.org/10.1002/(sici)1096-8628(20000103)90:1<29::aid-ajmg6>3.0.co
https://doi.org/10.1002/(sici)1096-8628(20000103)90:1<29::aid-ajmg6>3.0.co
Autor:
Howard M. Saal, A. Milatovich-Cherry, R.I. Blough, Steven D. Chernausek, S. Dey, Kim N. Dietrich, Elizabeth K. Schorry
Publikováno v:
American Journal of Medical Genetics. 77:257-260
We present two sibs with partial trisomy 1 (q31.1-q32.1) due to a familial insertion. Patient 1 is a girl who presented at age 9 months with minor anomalies, short stature, and normal psychomotor development. Karyotype was 46,XX,der(4)ins(4;1) (p14;q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e9e0feef4e8b8db24a80f89064333c1
https://doi.org/10.1002/(sici)1096-8628(19980526)77:4<257::aid-ajmg1>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19980526)77:4<257::aid-ajmg1>3.0.co
Autor:
Athena Milatovich, Howard M. Saal, E. Schorry, M. Bofinger, C. Jayne, H. J. Stern, Robert J. Hopkin
Publikováno v:
American Journal of Medical Genetics. 70:377-386
Deletions of chromosome 6q are rare. We report 3 new patients with 6q deletions. Case 1 is a male with an interstitial deletion [del(6)(q13q14.2)], hypotonia, speech delays, and minor anomalies. Case 2 is a male with an interstitial deletion [del(6)(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5683768c56c64ff1f0f811c47d66d30
https://doi.org/10.1002/(sici)1096-8628(19970627)70:4<377::aid-ajmg9>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19970627)70:4<377::aid-ajmg9>3.0.co
Publikováno v:
Prenatal Diagnosis. 16:857-861
A patient with ring chromosome 6/monosomy 6 mosaicism is presented. At 25 weeks' gestation, ultrasound examination demonstrated fetal hydrocephalus. Amniocentesis was performed. The fetal karyotype was 45,XY,-6/ 45,XY,-6,+f/46,XY,r(6)(p25q27). Delive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a8d59661b49978e160477ab9aae36e7
https://doi.org/10.1002/(sici)1097-0223(199609)16:9<857::aid-pd950>3.0.co
https://doi.org/10.1002/(sici)1097-0223(199609)16:9<857::aid-pd950>3.0.co
Autor:
G.M. Landes, J.M. Bishop, J. Louhimo, M.L. Freeman, S.S. Kakar, K. Sudo, P. Kunapuli, X. Li, M.R.S. Krishnamani, M.E. Curran, H. Hayes, D.C. Ward, K.W. Gripp, R. Iida, L.A. Pérez Jurado, N. Hayashi, M. Amagai, U. Francke, D. Nadano, M.L. Summar, K. Omoe, M. Aronson, H. Nagase, T. Ishida, K. Ohata, S.C. Maric, B. Dutrillaux, F. Apiou, D.F. Callen, D.W. Bell, G. Goubin, Y. Nakamura, E. Takahashi, B. Schlegelberger, P.N. Tsichlis, H. Hameister, C. Van Broeckhoven, J. Kudoh, E.L.D. Mitchell, E. Sierra-Rivera, S.M. Gartler, M. Schertzer, M. Ogawa, J.L. Benovic, H. Mizusawa, H. Sugawara, C.A. Griffin, N.A. Jenkins, S. Shin, H.L. Grimes, C.I. Civin, M. Yerle, S. Hoyer-Fender, K. Chinen, E. Shtivelman, H. Arakawa, L.A. Cannizzaro, K. Kishi, J.M. Varley, L. Pibouin, H. Yasue, F. Bullrich, Y.-J. Chen, J. Lasota, E.P. Cribiu, M.F. Santibanez Koref, G.R.M. White, S.A. Lane, T. Itoh, D.J. Gilbert, Y. Murakami, J.R. Testa, D. Jones, O.A. Jänne, W. Grote, M.L. Yaremko, M. Poetsch, H. Takeshita, E. Kim, T. Yasuda, T. Sofuni, T. Druck, J.M. Delabar, S. Ueda, T. Eki, N. Shimizu, K. Weber-Matthiesen, C.B. Gilks, K. Huebner, C. Le Chalony, D. Small, N.G. Copeland, H. Ishikawa, A. Endo, P. Burfeind, M. Ohki, Y. Lahbib-Mansas, J. Deerberg, Y. Sakaki, M.T. Keating, H. Tanabe, H.D. Webb, E.Y. Cheng, Y. Wang, C.E. Carow, E.W. Jabs, J. Gellin, T. Nishikawa, A. Milatovich, M. Nagata, T. Fujiwara, S. Suwa, S. Minoshima, J.A. Phillips, T. Hashimoto, S. Wood, M. Dasouki, A.L. Hawkins, F. Claro, R. Peoples, A. Crozat, T. Taguchi, M. Banzai, S. Antonarakis, J. Gomez, P. Zweidler-McKay, T. Haaf, C. Mellink, D. Patterson, S. Knuutila, J.D. Neill
Publikováno v:
Cytogenetic and Genome Research. 70:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daec3f414df3e80fc6c1fe3cb52e055f
https://doi.org/10.1159/000134026
https://doi.org/10.1159/000134026
Autor:
A. Milatovich, Neal G. Copeland, Karen J. Moore, Joseph R. Testa, Nancy A. Jenkins, Uta Francke
Publikováno v:
Cytogenetic and Genome Research. 69:53-58
Sequences encoding 1,235 bp of the human myosin heavy chain 12 (MYH12) gene have been cloned from a human brain cDNA library by PCR amplification. The human sequence is 95.8% identical to the mouse sequence at the amino acid level, indicating that th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5890aad247378cb08bf9752b0d7a546a
https://doi.org/10.1159/000133937
https://doi.org/10.1159/000133937
Publikováno v:
Somatic Cell and Molecular Genetics. 20:75-86
Cyclic nucleotides are important second messengers that mediate a number of cellular responses to external signals. Cyclic nucleotide phosphodiesterases play a role in signal transduction by regulating the cellular concentrations of these messengers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c16a209800cd8c2c00cc093fb99c78ee
https://doi.org/10.1007/bf02290677
https://doi.org/10.1007/bf02290677
Autor:
Michael S. Brown, Douglas A. Andres, Uta Francke, Janet M. Wenzlau, Athena Milatovich, Tayfun Ozcelik, Joseph L. Goldstein
Publikováno v:
Genomics. 18:105-112
The CAAX farnesyltransferase is a heterodimeric enzyme that attaches a farnesyl group to a single cysteine in several cellular proteins. Substrates include the p21ras proteins, nuclear lamins, and several retinal proteins, all of which end with a "CA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fb9cb268852925ae09d866341128cb1
https://doi.org/10.1006/geno.1993.1432
https://doi.org/10.1006/geno.1993.1432
Autor:
A N McKenzie, X Li, D A Largaespada, A Sato, A Kaneda, S M Zurawski, E L Doyle, A Milatovich, U Francke, N G Copeland
Publikováno v:
The Journal of Immunology. 150:5436-5444
The genomic structure of the recently described cytokine IL-13 has been determined for both human and mouse genes. The nucleotide sequence of a 4.6-kb DNA segment of the human gene is described. The human IL-13 gene (IL13) occurs as a single copy in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::670f64dc7b88d2ac1c2f44048f61a037
https://doi.org/10.4049/jimmunol.150.12.5436
https://doi.org/10.4049/jimmunol.150.12.5436