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Wyszukujesz frazę ""Chromosomes, Human, Pair 1"" wg kryterium: Temat


Tytuł:
Characterization of a novel acquired der(1)del(1)(p13p31)t(1;15)(q42;q15) in a high risk t(12;21)-positive acute lymphoblastic leukemia.
Autorzy:
Kjeldsen E; Hemodiagnostic Laboratory, Cancer Cytogenetics Section, Department of Hematology, Aarhus University Hospital, Tage-Hansens Gade 2, DK-8000 Aarhus C, Denmark. Electronic address: .
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Źródło:
Gene [Gene] 2016 Dec 20; Vol. 595 (1), pp. 39-48. Date of Electronic Publication: 2016 Sep 21.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Base Sequence*
Sequence Deletion*
Translocation, Genetic*
Chromosomes, Human, Pair 1/*genetics
Chromosomes, Human, Pair 15/*genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Adolescent ; Adult ; Humans ; Male
Czasopismo naukowe
Tytuł:
Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review.
Autorzy:
Lim G; Department of Laboratory Medicine, School of Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-702, Korea.
Kim MJ
Oh SH
Cho SY
Lee HJ
Suh JT
Lee J
Lee WI
Cho KS
Park TS
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Dec; Vol. 203 (2), pp. 187-92.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 3*
Translocation, Genetic*
Leukemia, Myeloid, Acute/*genetics
Thrombocytosis/*genetics
Adult ; Aged ; Bone Marrow Cells/cytology ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
A novel case of t(X;1)(p11.2;p34) in a renal cell carcinoma with TFE3 rearrangement and favorable outcome in a 57-year-old patient.
Autorzy:
Haudebourg J; Department of Pathology, Nice University Hospital, 33 Avenue Valombrose, Nice Cedex 1, France. />Hoch B
Fabas T
Burel-Vandenbos F
Carpentier X
Amiel J
Cardot-Leccia N
Michiels JF
Pedeutour F
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Jul 15; Vol. 200 (2), pp. 75-8.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, X*
Gene Rearrangement*
Translocation, Genetic*
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors/*genetics
Carcinoma, Renal Cell/*genetics
Kidney Neoplasms/*genetics
Carcinoma, Renal Cell/pathology ; Female ; Humans ; Kidney Neoplasms/pathology ; Middle Aged
Czasopismo naukowe
Tytuł:
Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.
Autorzy:
Lunghi M; Division of Hematology, Amedeo Avogadro University of Eastern Piedmont and Ospedale Maggiore della Carità, Via Solaroli 17, 28100 Novara, Italy. />Casorzo L
De Paoli L
Riccomagno P
Rossi D
Gaidano G
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2010 Jan 01; Vol. 196 (1), pp. 89-92.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 16*
Translocation, Genetic*
Myelodysplastic Syndromes/*genetics
Aged, 80 and over ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male
Czasopismo naukowe
Tytuł:
A novel t(1;2)(p33;q33) in secondary postpolycythemic myelofibrosis.
Autorzy:
Panani AD
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Dec; Vol. 195 (2), pp. 201-2.
Typ publikacji:
Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 2*
Translocation, Genetic*
Polycythemia/*genetics
Primary Myelofibrosis/*genetics
Humans ; Karyotyping ; Polycythemia/complications ; Primary Myelofibrosis/complications
Opinia redakcyjna
Tytuł:
t(1;16)(q10;p10) as the sole karyotypic abnormality in acute myeloid leukemia.
Autorzy:
Takahashi T
Suzuki M
Tsukuda H
Kimura H
Yoshimoto M
Tsujisaki M
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Jul; Vol. 192 (1), pp. 52-3.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 16*
Translocation, Genetic*
Leukemia, Myeloid, Acute/*genetics
Aged ; Chromosome Aberrations ; Female ; Humans
Raport
Tytuł:
Derivative (1)t(1;19)(p13;p13) in the setting of myelofibrosis with JAK2 V617F.
Autorzy:
Staropoli JF
Wadleigh M
Dal Cin P
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2009 Jun; Vol. 191 (2), pp. 109-10.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Janus Kinase 2/*genetics
Primary Myelofibrosis/*genetics
Thrombocytosis/*genetics
Adult ; Amino Acid Substitution ; Bone Marrow/pathology ; Chromosome Mapping ; Female ; Humans ; Karyotyping ; Metaphase/genetics ; Primary Myelofibrosis/pathology ; Thrombocytosis/pathology ; Trisomy/genetics
Raport
Tytuł:
Imatinib resistance in a novel translocation der(17)t(1;17)(q25;p13) with loss of TP53 but without BCR/ABL kinase domain mutation in chronic myelogenous leukemia.
Autorzy:
Yamamoto K; Hematology/Oncology, Department of Medicine, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan.
Yakushijin K
Nishikawa S
Minagawa K
Katayama Y
Shimoyama M
Matsui T
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 May; Vol. 183 (1), pp. 77-81.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 17*
Genes, p53*
Translocation, Genetic*
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*drug therapy
Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*genetics
Piperazines/*therapeutic use
Protein-Tyrosine Kinases/*genetics
Pyrimidines/*therapeutic use
Adult ; Benzamides ; Disease Progression ; Drug Resistance, Neoplasm/genetics ; Fusion Proteins, bcr-abl ; Gene Deletion ; Genes, abl ; Humans ; Imatinib Mesylate ; Male ; Mutation ; Protein Structure, Tertiary/genetics ; Protein-Tyrosine Kinases/chemistry
Czasopismo naukowe
Tytuł:
Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo.
Autorzy:
Macedo Silva ML; National Center for Bone Marrow Transplant, National Cancer Institute, Rio de Janeiro, Brazil. />Raimondi SC
Abdelhay E
Gross M
Mkrtchyan H
de Figueiredo AF
Ribeiro RC
de Jesus Marques-Salles T
Sobral ES
Gerardin Land MP
Liehr T
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 Apr 01; Vol. 182 (1), pp. 56-60.
Typ publikacji:
Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 16*
Oncogene Proteins, Fusion*
Translocation, Genetic*
Leukemia, Myelomonocytic, Acute/*genetics
Chromosome Banding ; Humans ; In Situ Hybridization, Fluorescence ; Infant ; Karyotyping ; Male
Czasopismo naukowe
Tytuł:
Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2.
Autorzy:
Ahmad F; Research and Development, SRL Ranbaxy Ltd., MIDC, Andheri (E), Mumbai-400093, India.
Kokate P
Chheda P
Dalvi R
Das BR
Mandava S
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2008 Jan 15; Vol. 180 (2), pp. 153-7.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 21*
Chromosomes, Human, Pair 8*
Translocation, Genetic*
Core Binding Factor Alpha 2 Subunit/*genetics
Leukemia, Myeloid, Acute/*genetics
Oncogene Proteins, Fusion/*genetics
Base Sequence ; Chromosome Mapping ; Cytogenetic Analysis ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Middle Aged ; RUNX1 Translocation Partner 1 Protein
Czasopismo naukowe
Tytuł:
A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia.
Autorzy:
Park TS; Department of Laboratory Medicine, Yonsei University College of Medicine, 250 Seongsanno, Seodaemun-gu, Seoul 120-752, Korea.
Song J
Lee KA
Lee SG
Yoon S
Kim JS
Lyu CJ
Choi JR
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Dec; Vol. 179 (2), pp. 132-5.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 15*
Translocation, Genetic*
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Child ; Humans ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Rare t(1;11)(q23;p15) in therapy-related myelodysplastic syndrome evolving into acute myelomonocytic leukemia: a case report and review of the literature.
Autorzy:
Zhang L; Department of Pathology and Laboratory, Cedars Sinai Medical Center, 8700 Beverly Boulevard, Room 4711, Los Angeles, CA 90048, USA. />Alsabeh R
Mecucci C
La Starza R
Gorello P
Lee S
Lill M
Schreck R
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Oct 01; Vol. 178 (1), pp. 42-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
Translocation, Genetic*
Leukemia, Myelomonocytic, Acute/*genetics
Myelodysplastic Syndromes/*genetics
Myelodysplastic Syndromes/*pathology
Myelodysplastic Syndromes/*therapy
Adult ; Aged ; Disease Progression ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged ; Neutrophils/metabolism
Czasopismo naukowe
Tytuł:
Molecular cytogenetic analysis of complex karyotypes with derivative chromosome der(1)t(1;5) found in two patients with myeloid leukemia.
Autorzy:
Melichercíková J; Institute of Hematology and Blood Transfusion, U Nemocnice 1, 128 20 Prague 2, Czech Republic.
Brezinová J
Zemanová Z
Cermák J
Michalová K
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Jul 15; Vol. 176 (2), pp. 150-5.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 5*
Translocation, Genetic*
Leukemia, Myeloid/*genetics
Adult ; Cytogenetic Analysis ; Humans ; Karyotyping ; Male ; Middle Aged ; Tumor Cells, Cultured
Czasopismo naukowe
Tytuł:
Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia.
Autorzy:
Crescenzi B; Department of Hematology, University of Perugia, IBiT Foundation (Fondazione IRCCS Biotecnologie nel Trapianto), via Brunamonti 51, 06122 Perugia, Italy.
La Starza R
Nozzoli C
Ciolli S
Matteucci C
Romoli S
Rigacci L
Gorello P
Bosi A
Martelli MF
Marynen P
Mecucci C
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Jul 01; Vol. 176 (1), pp. 67-71.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 12*
Chromosomes, Human, Pair 5*
Translocation, Genetic*
Leukemia, Myelomonocytic, Chronic/*genetics
Oncogene Proteins, Fusion/*genetics
Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Endometrioid-like yolk sac and Sertoli-Leydig cell tumors in a carrier of a Y heterochromatin insertion into 1qh region: a causal association?
Autorzy:
Sala E; Genetic Laboratory, H.S. Gerardo, Monza, Italy.
Villa N
Crosti F
Miozzo M
Perego P
Cappellini A
Bonazzi C
Barisani D
Dalprà L
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2007 Mar; Vol. 173 (2), pp. 164-9.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Y*
Endodermal Sinus Tumor/*pathology
Ovarian Neoplasms/*pathology
Sertoli-Leydig Cell Tumor/*pathology
Translocation, Genetic/*genetics
Carcinoma, Endometrioid/pathology ; Chromosome Mapping/methods ; Endodermal Sinus Tumor/genetics ; Female ; Heterochromatin/genetics ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Loss of Heterozygosity ; Ovarian Neoplasms/genetics ; Sequence Tagged Sites ; Sertoli-Leydig Cell Tumor/genetics
Czasopismo naukowe
Tytuł:
A rare case of acute myeloid leukemia evolving from a myelodysplastic syndrome with der(19)t(1;19).
Autorzy:
Pinheiro RF
Chauffaille Mde L
Silva MR
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Sep; Vol. 169 (2), pp. 181-3.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Leukemia, Myeloid/*genetics
Myelodysplastic Syndromes/*complications
Acute Disease ; Adult ; Aged ; Female ; Humans ; Leukemia, Myeloid/etiology
Raport
Tytuł:
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9).
Autorzy:
Sambani C; Laboratory of Health Physics & Environmental Hygiene, NCSR Demokritos, 15310 Aghia Paraskevi, Athens, Greece. />La Starza R
Pierini V
Vandenberghe P
Gonzales-Aguilera JJ
Rigana H
Koumbi D
Manola KN
Stavropoulou C
Georgakakos VN
Pagoni M
Wlodarska I
Mecucci C
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Oct 01; Vol. 162 (1), pp. 45-9.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 9*
Translocation, Genetic*
Myeloproliferative Disorders/*genetics
Aged ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Jumping translocations in multiple myeloma.
Autorzy:
Jamet D; Laboratoire d'Histologie, Embryologie et Cytogénétique, Faculté de Médecine et des Sciences de la Santé, Université de Bretagne Occidentale, 22 Avenue Camille Desmoulins, Brest cedex F-29285, France.
Marzin Y
Douet-Guilbert N
Morel F
Le Bris MJ
Herry A
Banzakour S
Bourquard P
Morice P
Abgrall JF
Berthou C
De Braekeleer M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Sep; Vol. 161 (2), pp. 159-63.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Translocation, Genetic*
Multiple Myeloma/*genetics
Aged ; Female ; Humans ; In Situ Hybridization, Fluorescence/methods ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
A der(14)t(1;14)(q12;p11) in chronic myelomonocytic leukemia.
Autorzy:
Djordjevic V; Institute of Hematology, Clinical Center of Serbia, Koste Todorovića 2, 11000 Belgrade, Serbia and Montenegro. />Jankovic G
Suvajdzic N
Marisavljevic D
Pantic M
Bogdanovic A
Sefer D
Dencic M
Colovic M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Jul 01; Vol. 160 (1), pp. 89-93.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 14*
Translocation, Genetic*
Leukemia, Myelomonocytic, Chronic/*genetics
Adult ; Humans ; Male ; Trisomy
Czasopismo naukowe
Tytuł:
Translocation (1;4;12)(q25;q27;q15) in a childhood intramuscular lipoma.
Autorzy:
Bao L
Miles L
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Apr 01; Vol. 158 (1), pp. 95-7.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 12*
Chromosomes, Human, Pair 4*
Translocation, Genetic*
Lipoma/*genetics
Muscle Neoplasms/*genetics
Child ; Female ; Humans ; Karyotyping
Raport

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