Výsledky vyhledávání - "R S, Kucherlapati"

Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases

Autor: H, Kobayashi, K T, Montgomery, S K, Bohlander, C N, Adra, B L, Lim, R S, Kucherlapati, H, Donis-Keller, M S, Holt, M M, Le Beau, J D, Rowley

Publikováno v: Blood. 84:3473-3482

Translocations and deletions of the short arm of chromosome 12 [t(12p) and del(12p)] are common recurring abnormalities in a broad spectrum of hematologic malignant diseases. We studied 20 patients and one cell line whose cells contained 12p13 transl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0dfcf4a961f8093e234e323fb242d5a
https://doi.org/10.1182/blood.v84.10.3473.bloodjournal84103473

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Heterogeneity in the breakpoints in balanced rearrangements involving band 12p13 in hematologic malignancies identified by fluorescence in situ hybridization: TEL (ETV6 ) is involved in only one half

Autor: Y, Sato, S K, Bohlander, H, Kobayashi, S, Reshmi, Y, Suto, E M, Davis, R, Espinosa, R, Hoopes, K T, Montgomery, R S, Kucherlapati, M M, Le Beau, J D, Rowley

Publikováno v: Blood. 90(12)

Using fluorescence in situ hybridization (FISH) and probes located on 12p12.1 to 13.3, we studied the breakpoints of 23 patients who had various hematologic malignant diseases and who had 12p13-balanced translocations (21 patients), inversion (1 pati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bb69e4618ce4166e14222efd08a311cc
https://pubmed.ncbi.nlm.nih.gov/9389705

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Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas

Autor: M, Schoenberg Fejzo, H R, Ashar, K S, Krauter, W L, Powell, M S, Rein, S, Weremowicz, S J, Yoon, R S, Kucherlapati, K, Chada, C C, Morton

Publikováno v: Genes, chromosomescancer. 17(1)

Uterine leiomyomata are the most common pelvic tumors in women and are the indication for more than 200,000 hysterectomies annually in the United States. Rearrangement of chromosome 12 in bands q14-q15 is characteristic of uterine leiomyomata and oth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4f541aac0361cf79380001e68389fba2
https://pubmed.ncbi.nlm.nih.gov/8889500

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Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions

Autor: E A, Lindsay, R, Goldberg, V, Jurecic, B, Morrow, C, Carlson, R S, Kucherlapati, R J, Shprintzen, A, Baldini

Publikováno v: American journal of medical genetics. 57(3)

Velo-cardio-facial (VCFS) or Shprintzen syndrome is associated with deletions in a region of chromosome 22q11.2 also deleted in DiGeorge anomaly and some forms of congenital heart disease. Due to the variability of phenotype, the evaluation of the in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a0b6824a7dd84fa1d0b759bb7a62564a
https://pubmed.ncbi.nlm.nih.gov/7677167

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Homologous Recombination Catalyzed by Human Cell Extracts

Autor: R S, Kucherlapati, J, Spencer, P D, Moore

Publikováno v: Molecular and Cellular Biology. 5:714-720

Two plasmids containing noncomplementing and nonreverting deletions in a bacterial phosphotransferase gene conferring resistance to neomycin (Neor) were incubated with human cell extracts, and the mixtures were used to transform recombination-deficie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9e66b6b1f2b0c816d005a35ba3435f2
https://doi.org/10.1128/mcb.5.4.714-720.1985

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Mammalian chromosome identification in interspecific hybride cells using 'Hoechst 33258'

Autor: R S, Kucherlapati, I, Hilwig, A, Gropp, F H, Ruddle

Publikováno v: Humangenetik. 27(1)

Treatment of fixed chromosome preparations of mouse-human hybrid cells with the benzimidazol derivative "Hoechst 33258" makes it possible to distinguish between mouse and human chromosomes. Treatment of live cells results in differential condensation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::973e0a48e49acde21a9e0a3463589860
https://pubmed.ncbi.nlm.nih.gov/49289

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beta2-microglobulin locus on human chromosome 15

Autor: H E, Faber, R S, Kucherlapati, M D, Poulik, F H, Ruddle, O, Smithies

Publikováno v: Somatic cell genetics. 2(2)

We have developed an autoradiographic/electrophoretic assay capable of distinguishing mouse and human beta2-microglobulin (beta2m) in spent culture media. The method is applicable to mouse and human lines and to hybrid cell lines made from them. With

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e4d8958caab35ba510587c586302ab58
https://pubmed.ncbi.nlm.nih.gov/69326

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