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


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:
Molecular cytogenetic analysis of chromosomes 1 and 19 in glioma cell lines.
Autorzy:
Law ME; Department of Laboratory Medicine and Pathology, Division of Laboratory Genetics, Mayo Clinic and Foundation, 200 First Street SW, Rochester, MN 55905, USA.
Templeton KL
Kitange G
Smith J
Misra A
Feuerstein BG
Jenkins RB
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Jul 01; Vol. 160 (1), pp. 1-14.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Loss of Heterozygosity*
Glioma/*genetics
Cell Line, Tumor ; Humans ; In Situ Hybridization, Fluorescence ; PTEN Phosphohydrolase ; Phosphoric Monoester Hydrolases/genetics ; Polymerase Chain Reaction ; Tumor Suppressor Proteins/genetics
Czasopismo naukowe
Tytuł:
Inv(1)(p22q25) in chronic myeloproliferative disease: constitutional or clonal defect?
Autorzy:
Wong KF; Department of Pathology, Queen Elizabeth Hospital, 30 Gascoigne Road, Hong Kong SAR, China. />Wong WC
Cheuk W
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Apr 15; Vol. 158 (2), pp. 188-91.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Chromosome Inversion*
Chromosomes, Human, Pair 1*
Myeloproliferative Disorders/*genetics
Aged ; Chromosome Banding ; Humans ; Karyotyping ; Male ; Middle Aged ; Myeloproliferative Disorders/pathology
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
Tytuł:
Jumping translocation of 1q in a BCR/ABL-positive acute lymphoblastic leukemia.
Autorzy:
Pelz AF; Institute of Human Genetics, Otto-von-Guericke University of Magdeburg, Leipziger Strasse 44, H.26, D-39120 Magdeburg, Germany. />Müller G
Wieacker P
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Mar; Vol. 157 (2), pp. 157-9.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Translocation, Genetic*
Fusion Proteins, bcr-abl/*metabolism
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Aged ; Chromosomes, Human, Pair 22 ; Chromosomes, Human, Pair 3 ; Chromosomes, Human, Pair 8 ; Humans ; Karyotyping ; Male
Czasopismo naukowe
Tytuł:
Rearrangement of the MLL gene in acute myeloblastic leukemia: report of two rare translocations.
Autorzy:
Douet-Guilbert N; Laboratoire d'Histologie, Embryologie et Cytogénétique, Faculté de Médecine et des Sciences de la Santé, Université de Bretagne Occidentale 22, avenue Camille Desmoulins CS 93837, F-29238, Brest cedex 3, France.
Morel F
Le Bris MJ
Herry A
Morice P
Bourquard P
Banzakour S
Le Calvez G
Marion V
Berthou C
De Braekeleer M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Mar; Vol. 157 (2), pp. 169-74.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
Chromosomes, Human, Pair 17*
Translocation, Genetic*
DNA-Binding Proteins/*genetics
Leukemia, Myeloid, Acute/*genetics
Proto-Oncogenes/*genetics
Transcription Factors/*genetics
Adult ; Histone-Lysine N-Methyltransferase ; Humans ; Karyotyping ; Male ; Middle Aged ; Myeloid-Lymphoid Leukemia Protein
Czasopismo naukowe
Tytuł:
Molecular cytogenetic study of instability at 1q21 approximately q32 in adult acute lymphoblastic leukemia.
Autorzy:
Specchia G; Hematology, University of Foggia, Foggia, Italy. />Albano F
Anelli L
Zagaria A
Liso A
Pannunzio A
Archidiacono N
Liso V
Rocchi M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Jan 01; Vol. 156 (1), pp. 54-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Middle Aged ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology
Czasopismo naukowe
Tytuł:
Cytogenetic abnormalities in hepatoblastoma: report of two new cases and review of the literature suggesting imbalance of chromosomal regions on chromosomes 1, 4, and 12.
Autorzy:
Nagata T; Department of Advanced Medicine, Nihon University, School of Medicine, 30-1 Oyaguchikami-cho, Itabashi-ku, Tokyo 173-8610, Japan. />Nakamura M
Shichino H
Chin M
Sugito K
Ikeda T
Koshinaga T
Fukuzawa M
Inoue M
Mugishima H
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Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2005 Jan 01; Vol. 156 (1), pp. 8-13.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 12*
Chromosomes, Human, Pair 4*
Hepatoblastoma/*genetics
Liver Neoplasms/*genetics
Aneuploidy ; Child, Preschool ; Female ; Humans ; Infant ; Male ; Translocation, Genetic
Czasopismo naukowe
Tytuł:
Identification of a novel t(1;9)(q11;q34) in acute myelocytic leukemia.
Autorzy:
Piccaluga PP
Luatti S
Ascani S
Bianchini M
Malagola M
Rondoni M
Gaitani S
Testoni N
Pileri SA
Baccarani M
Martinelli G
Visani G
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2004 May; Vol. 151 (1), pp. 85-6.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 9*
Translocation, Genetic*
Leukemia, Myeloid, Acute/*genetics
Female ; Humans ; Immunophenotyping ; Karyotyping ; Leukemia, Myeloid, Acute/immunology ; Middle Aged
Raport
Tytuł:
Genetic and pathologic significance of 1p, 17p, and 18q aneusomy and the ERBB2 gene in colorectal cancer and related normal colonic mucosa.
Autorzy:
Cianciulli A; Department of Clinical Pathology, Regina Elena Cancer Institute, IFO Via Elio Chianesi 53, 00144 Rome, Italy. />Cosimelli M
Marzano R
Merola R
Piperno G
Sperduti I
de la Iglesia F
Leonardo G
Graziano F
Mancini R
Guadagni F
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2004 May; Vol. 151 (1), pp. 52-9.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 17*
Chromosomes, Human, Pair 18*
Genes, erbB-2*
Colon/*metabolism
Colorectal Neoplasms/*genetics
Adult ; Aged ; Aged, 80 and over ; Female ; Gene Amplification ; Humans ; In Situ Hybridization, Fluorescence ; Intestinal Mucosa/metabolism ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Association of loss of 1p and alterations of chromosome 14 in meningioma progression.
Autorzy:
Lopez-Gines C; Department of Pathology, Medical School, University of Valencia, Avda. Blasco Ibáñez 17, 46010 Valencia, Spain. />Cerda-Nicolas M
Gil-Benso R
Callaghan R
Collado M
Roldan P
Llombart-Bosch A
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2004 Jan 15; Vol. 148 (2), pp. 123-8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 14*
Meningioma/*genetics
Adult ; Aged ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Male ; Middle Aged ; Monosomy
Czasopismo naukowe
Tytuł:
Centromeric transverse fission of chromosome 1 in a case of acute myelocytic leukemia.
Autorzy:
Bakshi SR
Roy SK
Patel SJ
Trivedi PJ
Brahmbhatt M
Patel SM
Shah PM
Patel DD
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Oct 15; Vol. 146 (2), pp. 173-5.
Typ publikacji:
Letter
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Leukemia, Myeloid, Acute/*genetics
Humans ; Karyotyping ; Male ; Middle Aged
Opinia redakcyjna
Tytuł:
A novel translocation der(4)t(1;4)(q21;q35) and a marker chromosome in a case of myelodysplastic syndrome.
Autorzy:
Vundinti BR
Madkaikar M
Kerketta L
Jijina F
Ghosh K
Mohanty D
Jijina F
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jul 15; Vol. 144 (2), pp. 175-6.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 4*
Translocation, Genetic*
Myelodysplastic Syndromes/*genetics
Adult ; Humans ; Male
Raport
Tytuł:
Loss of 1p and 7p in radiation-induced meningiomas identified by comparative genomic hybridization.
Autorzy:
Rajcan-Separovic E; Cytogenetics Laboratory, Department of Pathology, University of British Columbia, BC Children's Hospital, Vancouver, BC, Canada. />Maguire J
Loukianova T
Nisha M
Kalousek D
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jul 01; Vol. 144 (1), pp. 6-11.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 7*
Meningioma/*genetics
Neoplasms, Radiation-Induced/*genetics
Nucleic Acid Hybridization/*methods
Adult ; Aged ; Base Sequence ; DNA Primers ; Female ; Humans ; Male ; Middle Aged
Czasopismo naukowe
Tytuł:
Interphase cytogenetic characterization of aberrations in the long arm of chromosome 1 in B-cell lymphoid malignancies.
Autorzy:
Weng L
Gesk S
Martín-Subero JI
Harder L
Schlegelberger B
Grote W
Siebert R
Dyer MJ
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jul 01; Vol. 144 (1), pp. 83-4.
Typ publikacji:
Letter; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Interphase*
Lymphoma, B-Cell/*genetics
Humans ; In Situ Hybridization, Fluorescence
Raport
Tytuł:
Detection by fluorescence in situ hybridization of microdeletions at 1p36 in lymphomas, unidentified on cytogenetic analysis.
Autorzy:
Rajgopal A; Molecular Medicine Unit, St. James's University Hospital, Leeds LS9 7TF, UK.
Carr IM
Leek JP
Hodge D
Bell SM
Roberts P
Horgan K
Bonthron DT
Selby PJ
Markham AF
MacLennan KA
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Apr 01; Vol. 142 (1), pp. 46-50.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
In Situ Hybridization, Fluorescence/*methods
Lymphoma/*genetics
Adolescent ; Adult ; Aged ; Cytogenetic Analysis ; Female ; Humans ; Male ; Middle Aged ; Sensitivity and Specificity
Czasopismo naukowe
Tytuł:
A consistent region of deletion on 1p36 in meningiomas: identification and relation to malignant progression.
Autorzy:
Murakami M; Department of Neurosurgery, Kyoto Prefectural University of Medicine, Kyoto 602-8566, Japan.
Hashimoto N
Takahashi Y
Hosokawa Y
Inazawa J
Mineura K
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2003 Jan 15; Vol. 140 (2), pp. 99-106.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1/*ultrastructure
Meningeal Neoplasms/*genetics
Meningioma/*genetics
Adult ; Aged ; Alleles ; Biomarkers, Tumor/analysis ; Chromosomes, Human, Pair 1/genetics ; Disease Progression ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Ki-67 Antigen/analysis ; Ki-67 Antigen/genetics ; Loss of Heterozygosity ; Male ; Meningeal Neoplasms/pathology ; Meningioma/pathology ; Microsatellite Repeats ; Middle Aged ; Neoplasm Proteins/analysis ; Neoplasm Proteins/genetics
Czasopismo naukowe
Tytuł:
Structural chromosomal abnormality of 1q in acute leukemia with Sweet syndrome.
Autorzy:
Colovic M
Jankovic G
Suvajdzic N
Nikolic M
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Nov; Vol. 139 (1), pp. 84-5.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Leukemia, Myeloid, Acute/*genetics
Sweet Syndrome/*genetics
Adult ; Chromosome Banding ; Chromosome Mapping ; Female ; Humans ; Karyotyping ; Leukemia, Myeloid, Acute/complications ; Leukemia, Myeloid, Acute/pathology ; Sweet Syndrome/complications ; Sweet Syndrome/pathology
Raport
Tytuł:
Late appearance of t(1;19)(q11;q11) in myelodysplastic syndrome associated with dysplastic eosinophilia and pulmonary alveolar proteinosis.
Autorzy:
Ando J; Department of Hematology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Tamayose K
Sugimoto K
Oshimi K
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Nov; Vol. 139 (1), pp. 14-7.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Eosinophilia/*genetics
Myelodysplastic Syndromes/*genetics
Pulmonary Alveolar Proteinosis/*genetics
Bone Marrow Cells/pathology ; Chromosome Mapping ; DNA/blood ; DNA/genetics ; Eosinophilia/complications ; Eosinophilia/pathology ; Eosinophils/pathology ; Humans ; Karyotyping ; Male ; Metaphase ; Middle Aged ; Myelodysplastic Syndromes/complications ; Myelodysplastic Syndromes/pathology ; Pulmonary Alveolar Proteinosis/complications ; Pulmonary Alveolar Proteinosis/pathology
Czasopismo naukowe
Tytuł:
Partial deletion of chromosome 1 in a case of acute myelocytic leukemia.
Autorzy:
Coupland LA; Department of Clinical Haematology, The Canberra Hospital, Garran, Australia. />Jammu V
Pidcock ME
Pokaż więcej
Źródło:
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2002 Nov; Vol. 139 (1), pp. 60-2.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Leukemia, Myeloid, Acute/*genetics
Adult ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Humans ; Karyotyping ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/pathology ; Male ; Time Factors ; Treatment Outcome
Czasopismo naukowe

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