Works matching DE "COMPARATIVE genomic hybridization"

Results: 1643

Chromosomal imbalances in clear cell ependymomas.

Published in:

Modern Pathology, 2006, v. 19, n. 7, p. 958, doi. 10.1038/modpathol.3800614

By:

Rickert, Christian H.;
Korshunov, Andrey;
Paulus, Werner

Publication type:

Article

Clinical application of array-based comparative genomic hybridization to define the relationship between multiple synchronous tumors.

Published in:

Modern Pathology, 2005, v. 18, n. 4, p. 591, doi. 10.1038/modpathol.3800332

By:

Wa, Chrystal V.;
de Vries, Sandy;
Chen, Yunn Yi;
Waldman, Frederic M.;
Hwang, E. Shelley

Publication type:

Article

Comparative genomic hybridization analysis of thymic neuroendocrine tumors.

Published in:

Modern Pathology, 2005, v. 18, n. 3, p. 358, doi. 10.1038/modpathol.3800246

By:

Chin-Chen Pan;
Yiin-Jeng Jong;
Yann-Jang Chen

Publication type:

Article

CGH and CD 44/MIB-1 immunohistochemistry are helpful to distinguish metastasized from nonmetastasized sporadic pheochromocytomas.

Published in:

Modern Pathology, 2004, v. 17, n. 9, p. 1119, doi. 10.1038/modpathol.3800160

By:

August, Christian;
August, Kathrein;
Schroeder, Soeren;
Bahn, Hannes;
Hinze, Raoul;
Baba, Hideo A.;
Kersting, Christian;
Buerger, Horst

Publication type:

Article

Recurrent DNA copy number changes revealed by comparative genomic hybridization in primary Merkel cell carcinomas.

Published in:

Modern Pathology, 2004, v. 17, n. 5, p. 561, doi. 10.1038/modpathol.3800091

By:

Larramendy, Marcelo L.;
Koljonen, Virve;
Böhling, Tom;
Tukiainen, Erkii;
Knuutila, Sakari

Publication type:

Article

Simultaneous chromosome 1q gain and 16q loss is associated with steroid receptor presence and low proliferation in breast carcinoma.

Published in:

Modern Pathology, 2004, v. 17, n. 4, p. 449, doi. 10.1038/modpathol.3800059

By:

Farabegoli, Fulvia;
Hermsen, Mario AJA;
Ceccarelli, Claudio;
Santini, Donatella;
Weiss, Marianne M.;
Meijer, Gerrit A.;
van Diest, Paul J.

Publication type:

Article

Comparative genomic hybridization study of placental site trophoblastic tumour: a report of four cases.

Published in:

Modern Pathology, 2004, v. 17, n. 2, p. 248, doi. 10.1038/modpathol.3800025

By:

Hui, Pei;
Riba, Ali;
Pejovic, Tanja;
Johnson, Tulin;
Baergen, Rebecca N.;
Ward, David

Publication type:

Article

Loss of 13q14-q21 and Gain of 5p14-pter in the Progression of Leiomyosarcoma.

Published in:

Modern Pathology, 2003, v. 16, n. 8, p. 778, doi. 10.1097/01.MP.0000083648.45923.2B

By:

Wang, Rubin;
Titley, Jenny C.;
Yong-Jie Lu;
Summersgill, Brenda M.;
Bridge, Julia A.;
Fisher, Cyril;
Path, F. R. C.;
Shipley, Janet

Publication type:

Article

Most malignant fibrous histiocytomas developed in the retroperitoneum are dedifferentiated liposarcomas: a review of 25 cases initially diagnosed as malignant fibrous histiocytoma.

Published in:

2003

By:

Coindre, Jean-Michel;
Mariani, Odette;
Chibon, Frédéric;
Mairal, Aline;
de Saint Aubain Somerhausen, Nicolas;
Favre-Guillevin, Elizabeth;
Binh Bui, Nguyen;
Stoeckle, Eberhard;
Hostein, Isabelle;
Aurias, Alain;
Chibon, Frédéric;
Bui, Nguyen Binh

Publication type:

journal article

Identification of Four Distinct Regions of Allelic Imbalances on Chromosome 1 by the Combined Comparative Genomic Hybridization and Microsatellite Analysis on Hepatocellular Carcinoma.

Published in:

Modern Pathology, 2002, v. 15, n. 11, p. 1213, doi. 10.1097/01.MP.0000036347.66943.3C

By:

Thomas H.-Y. Leung;
Nathalie Wong;
Lai, Paul B.-S.;
Andrew Chan;
Ka-Fai To;
Choong-Tsek Liew;
Wan Yee Lau;
Johnson, Philip J.

Publication type:

Article

Chromosomal Imbalances in Diffuse Large B-Cell Lymphoma Detected by Comparative Genomic Hybridization.

Published in:

Modern Pathology, 2002, v. 15, n. 8, p. 807, doi. 10.1097/01.MP.0000024375.04135.2B

By:

Berglund, Mattias;
Enblad, Gunilla;
Flordal, Emma;
Lui, Weng-Onn;
Backlin, Carin;
Thunberg, Ulf;
Sundström, Christer;
Roos, Göran;
Allander, Susanne V.;
Erlanson, Martin;
Rosenquist, Richard;
Larsson, Catharina;
Lagercrantz, Svetlana

Publication type:

Article

The Potential Value of Comparative Genomic Hybridization Analysis in Effusion-and Fine Needle Aspiration Cytology.

Published in:

Modern Pathology, 2002, v. 15, n. 8, p. 818, doi. 10.1097/01.MP.0000024521.67720.0F

By:

Nagel, Holger;
Schulten, Hans Jürgen;
Gunawan, Bastian;
Brinck, Ulrich;
Füzesi, László

Publication type:

Article

DNA Copy Number Changes in Lung Adenocarcinoma in Younger Patients.

Published in:

Modern Pathology, 2002, v. 15, n. 4, p. 372, doi. 10.1038/modpathol.3880533

By:

Lindstrom, Irmeli;
Nordling, Stig;
Anna-Maria Nissén;
Tammilehto, Lauri;
Mattson, Karin;
Knuutila, Sakari

Publication type:

Article

Primary Soft Tissue Sarcoma and Its Local Recurrence: Genetic Changes Studied by Comparative Genomic Hybridization.

Published in:

Modern Pathology, 2001, v. 14, n. 10, p. 978, doi. 10.1038/modpathol.3880422

By:

Popov, Pentscho;
Virolainen, Mortti;
Tukiainen, Erkki;
Asko-Scljavaara, Sirpa;
Huuhtanen, Riikka;
Knuutila, Sakari;
Tarkkanen, Maija

Publication type:

Article

Unisexual and Heterosexual Meiotic Reproduction Generate Aneuploidy and Phenotypic Diversity <i>De Novo</i> in the Yeast <i>Cryptococcus neoformans</i>.

Published in:

PLoS Biology, 2013, v. 11, n. 9, p. 1, doi. 10.1371/journal.pbio.1001653

By:

Ni, Min;
Feretzaki, Marianna;
Li, Wenjun;
Floyd-Averette, Anna;
Mieczkowski, Piotr;
Dietrich, Fred S.;
Heitman, Joseph

Publication type:

Article

Clusters of Nucleotide Substitutions and Insertion/Deletion Mutations Are Associated with Repeat Sequences.

Published in:

PLoS Biology, 2011, v. 9, n. 6, p. 1, doi. 10.1371/journal.pbio.1000622

By:

McDonald, Michael J.;
Wang, Wei-Chi;
Huang, Hsien-Da;
Leu, Jun-Yi

Publication type:

Article

A simple method for enhancing hybridization efficiency in chromosome and array comparative genomic hybridization.

Published in:

Biotechnic & Histochemistry, 2011, v. 86, n. 3, p. 192, doi. 10.3109/10520291003666781

By:

Kawauchi, S;
Furuya, T;
Nakao, M;
Ikemoto, K;
Oga, A;
Sasaki, K

Publication type:

Article

A simple method for fixation and microdissection of frozen fresh tissue sections for molecular cytogenetic analysis of cancers.

Published in:

Biotechnic & Histochemistry, 2005, v. 80, n. 3/4, p. 147, doi. 10.1080/10520290500382806

By:

Huang, Q;
Sacks, PG;
Mo, J;
McCormick, SA;
Iacob, CE;
Guo, L;
Schaefer, S;
Schantz, SP

Publication type:

Article

DETECTING COPY NUMBER VARIATIONS FROM ARRAY CGH DATA BASED ON A CONDITIONAL RANDOM FIELD MODEL.

Published in:

Journal of Bioinformatics & Computational Biology, 2010, v. 8, n. 2, p. 295, doi. 10.1142/S021972001000480X

By:

YIN, XIAO-LIN;
LI, JING

Publication type:

Article

CLUSTERING OF MAIN ORTHOLOGS FOR MULTIPLE GENOMES.

Published in:

Journal of Bioinformatics & Computational Biology, 2008, v. 6, n. 3, p. 573, doi. 10.1142/S0219720008003540

By:

ZHENG FU;
TAO JIANG

Publication type:

Article

Comparative genomics of green sulfur bacteria.

Published in:

Photosynthesis Research, 2010, v. 104, n. 2/3, p. 137, doi. 10.1007/s11120-009-9515-2

By:

Davenport, Colin;
Ussery, David W.;
Tümmler, Burkhard

Publication type:

Article

Characterization and comparative genomic analysis of gamma-aminobutyric acid (GABA)-producing lactic acid bacteria from Thai fermented foods.

Published in:

Biotechnology Letters, 2021, v. 43, n. 8, p. 1637, doi. 10.1007/s10529-021-03140-y

By:

Phuengjayaem, Sukanya;
Booncharoen, Auttaporn;
Tanasupawat, Somboon

Publication type:

Article

Quantitation of non-amplified genomic DNA by bead-based hybridization and template mediated extension coupled to alkaline phosphatase signal amplification.

Published in:

Biotechnology Letters, 2010, v. 32, n. 2, p. 229, doi. 10.1007/s10529-009-0149-4

By:

Martins, S.;
Prazeres, D.;
Fonseca, L.;
Monteiro, G.

Publication type:

Article

Molecular signatures for the phylum (class) Thermotogae and a proposal for its division into three orders ( Thermotogales, Kosmotogales ord. nov. and Petrotogales ord. nov.) containing four families ( Thermotogaceae, Fervidobacteriaceae fam. nov., Kosmotogaceae fam. nov. and Petrotogaceae fam. nov.) and a new genus Pseudothermotoga gen. nov. with five new combinations

Published in:

Antonie van Leeuwenhoek, 2014, v. 105, n. 1, p. 143, doi. 10.1007/s10482-013-0062-7

By:

Bhandari, Vaibhav;
Gupta, Radhey

Publication type:

Article

Genetic diversity of Rhodopirellula strains.

Published in:

Antonie van Leeuwenhoek, 2013, v. 104, n. 4, p. 547, doi. 10.1007/s10482-013-0004-4

By:

Frank, Carsten;
Klockow, Christine;
Richter, Michael;
Glöckner, Frank;
Harder, Jens

Publication type:

Article

The role of genetic and epigenetic alterations in neuroblastoma disease pathogenesis.

Published in:

Pediatric Surgery International, 2013, v. 29, n. 2, p. 101, doi. 10.1007/s00383-012-3239-7

By:

Domingo-Fernandez, Raquel;
Watters, Karen;
Piskareva, Olga;
Stallings, Raymond;
Bray, Isabella

Publication type:

Article

cDNA microarray study to identify expression changes relevant for apoptosis in K562 cells co-treated with amifostine and imatinib.

Published in:

Cancer Chemotherapy & Pharmacology, 2007, v. 59, n. 3, p. 349, doi. 10.1007/s00280-006-0276-8

By:

Bianchini, Michele;
Martinelli, Giovanni;
Renzulli, Matteo;
Gonzalez Cid, Marcela;
Larripa, Irene

Publication type:

Article

Gain of 5p15.33 Is Associated with Progression of Bladder Cancer.

Published in:

Oncology, 2007, v. 72, n. 1/2, p. 132, doi. 10.1159/000111132

By:

Yamamoto, Yoshiaki;
Chochi, Yasuyo;
Matsuyama, Hideyasu;
Eguchi, Satoshi;
Kawauchi, Shigeto;
Furuya, Tomoko;
Oga, Atsunori;
Kang, Jason J.;
Naito, Katsusuke;
Sasaki, Kohsuke

Publication type:

Article

A Comparison of DNA Copy Number Changes Detected by Comparative Genomic Hybridization in Malignancies of the Liver, Biliary Tract and Pancreas.

Published in:

Oncology, 2001, v. 60, n. 2, p. 151, doi. 10.1159/000055313

By:

Shiraishi, Kei;
Okita, Kiwamu;
Kusano, Noriyoshi;
Harada, Tomohiko;
Kondoh, Satoshi;
Okita, Satoshi;
Ryozawa, Shomei;
Ohmura, Ryosuke;
Noguchi, Takayoshi;
Iida, Yozo;
Akiyama, Tetsuji;
Oga, Atsunori;
Fukumoto, Yohei;
Furuya, Tomoko;
Kawauchi, Shigeto;
Sasaki, Kohsuke

Publication type:

Article

Genetic Aberrations Detected by Comparative Genomic Hybridization in Ovarian Clear Cell Adenocarcinomas.

Published in:

Oncology, 2000, v. 59, n. 1, p. 50, doi. 10.1159/000012137

By:

Suehiro, Yutaka;
Sakamoto, Masaru;
Umayahara, Kenji;
Iwabuchi, Hiroshi;
Sakamoto, Hiroko;
Tanaka, Naotake;
Takeshima, Nobuhiro;
Yamauchi, Kazuhiro;
Hasumi, Katsuhiko;
Akiya, Tsukasa;
Sakunaga, Hotaka;
Muroya, Tetsuya;
Numa, Fumitaka;
Kato, Hiroshi;
Tenjin, Yoshio;
Sugishita, Tadashi

Publication type:

Article

Genetic Aberrations Detected by Comparative Genomic Hybridization in Biliary Tract Cancers.

Published in:

Oncology, 1999, v. 57, n. 1, p. 42, doi. 10.1159/000011999

By:

Shiraishi, Kei;
Kusano, Noriyoshi;
Okita, Satoshi;
Oga, Atsunori;
Okita, Kiwamu;
Sasaki, Kohsuke

Publication type:

Article

Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case–control study.

Published in:

Neuropsychopharmacology Reports, 2024, v. 44, n. 1, p. 42, doi. 10.1002/npr2.12370

By:

Lo, Tzuyao;
Kushima, Itaru;
Kimura, Hiroki;
Aleksic, Branko;
Okada, Takashi;
Kato, Hidekazu;
Inada, Toshiya;
Nawa, Yoshihiro;
Torii, Youta;
Yamamoto, Maeri;
Kimura, Ryo;
Funabiki, Yasuko;
Kosaka, Hirotaka;
Numata, Shusuke;
Kasai, Kiyoto;
Sasaki, Tsukasa;
Yokoyama, Shigeru;
Munesue, Toshio;
Hashimoto, Ryota;
Yasuda, Yuka

Publication type:

Article

Case reports of two siblings with autism spectrum disorder and 15q13.3 deletions.

Published in:

2023

By:

Furukawa, Sawako;
Kushima, Itaru;
Aleksic, Branko;
Ozaki, Norio

Publication type:

Case Study

Clinical characterization of patients with schizophrenia and 16p13.11 duplication: A case series.

Published in:

2023

By:

Kimura, Hiroki;
Kushima, Itaru;
Banno, Masahiro;
Inada, Toshiya;
Yoshimi, Akira;
Aleksic, Branko;
Ozaki, Norio

Publication type:

Case Study

Some Reflections about Electrical Status Epilepticus During Slow-Wave Sleep.

Published in:

Global Pediatric Health, 2022, p. 1, doi. 10.1177/2333794X221122726

By:

Posar, Annio;
Visconti, Paola

Publication type:

Article

Evaluation of utilization of amplified blastocoel fluid DNA gel electrophoresis band intensity as an additional minimally invasive approach in embryo selection: A cross-sectional study.

Published in:

International Journal of Reproductive Biomedicine, 2024, v. 22, n. 11, p. 907, doi. 10.18502/ijrm.v22i11.17823

By:

Khajehoseini, Fattaneh;
Noormohammadi, Zahra;
Eftekhari-Yazdi, Poopak;
Gourabi, Hamid;
Pazhoomand, Reza;
Hosseinishenatal, Shirzad;
Bazrgar, Masood

Publication type:

Article

Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report.

Published in:

International Journal of Reproductive Biomedicine, 2021, v. 19, n. 5, p. 477, doi. 10.18502/ijrm.v19i5.9258

By:

Mohammadi, Reza;
Taheri, Raheleh;
Shahriyari, Fatemeh;
Feiz, Farnaz;
Mohammadi, Zahra;
Shirian, Sadegh;
Raoofian, Reza;
Malekpour, Abdorrasoul;
Pazhoomand, Reza

Publication type:

Article

Investigation of the diagnostic value of chromosome analysis and bacterial artificial chromosome-based array comparative genomic hybridization in prenatal diagnosis.

Published in:

Turkish Journal of Medical Sciences, 2015, v. 45, n. 6, p. 1263, doi. 10.3906/sag-1312-161

By:

SAVLI, Hakan;
EREN KESKİN, Seda;
ÇİNE, Naci

Publication type:

Article

SNP array technology: an array of hope in breast cancer research.

Published in:

Malaysian Journal of Pathology, 2013, v. 35, n. 1, p. 33

By:

Ching Ching HO;
Kein-Seong MUN;
Rakesh NAIDU

Publication type:

Article

Recurrent human 16p11.2 microdeletions in type I Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome patients in Chinese Han population.

Published in:

Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2280

By:

Su, Kaizhen;
Liu, Han;
Ye, Xiaoqun;
Jin, Hangmei;
Xie, Zhenwei;
Yang, Chunbo;
Zhou, Daizhan;
Huang, Hefeng;
Wu, Yanting

Publication type:

Article

KBG syndrome: Clinical features and molecular findings in seven unrelated Korean families with a review of the literature.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 4, p. 1, doi. 10.1002/mgg3.2127

By:

Choi, Yunha;
Choi, Jungmin;
Do, Hyosang;
Hwang, Soojin;
Seo, Go Hun;
Choi, In Hee;
Keum, Changwon;
Choi, Jin‐Ho;
Kang, Minji;
Kim, Gu‐Hwan;
Yoo, Han‐Wook;
Lee, Beom Hee

Publication type:

Article

A novel partial de novo duplication of JARID2 gene causing a neurodevelopmental phenotype.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 11, p. 1, doi. 10.1002/mgg3.2037

By:

Viitasalo, Liisa;
Kettunen, Kaisa;
Kankainen, Matti;
Niemelä, Elina H.;
Kiiski, Kirsi

Publication type:

Article

Yield of array‐CGH analysis in Tunisian children with autism spectrum disorder.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 8, p. 1, doi. 10.1002/mgg3.1939

By:

Chehbani, Fethia;
Tomaiuolo, Pasquale;
Picinelli, Chiara;
Baccarin, Marco;
Castronovo, Paola;
Scattoni, Maria Luisa;
Gaddour, Naoufel;
Persico, Antonio M.

Publication type:

Article

Neurocognitive follow‐up in adult siblings with Phelan–McDermid syndrome due to a novel SHANK3 splicing site mutation.

Published in:

2021

By:

Kankuri‐Tammilehto, Minna;
Sauna‐aho, Oili;
Arvio, Maria

Publication type:

Case Study

8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 11, p. 1, doi. 10.1002/mgg3.1811

By:

Ben Ayed, Ikhlas;
Bouzid, Amal;
Kammoun, Fatma;
souissi, Amal;
Jallouli, Olfa;
Mallouli, Salma;
Guidara, Souhir;
Loukil, Salma;
Aloulou, Hajer;
Jbeli, Fida;
Aouichaoui, Sahar;
Abid, Dorra;
Abdelhedi, Fatma;
Triki, Chahnez;
Kamoun, Hassen;
Masmoudi, Saber

Publication type:

Article

CHL1 deletion is associated with cognitive and language disabilities – Case report and review of literature.

Published in:

Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 7, p. 1, doi. 10.1002/mgg3.1725

By:

Tsuboyama, Melissa;
Iqbal, Mohammed Anwar

Publication type:

Article

A 17q24.3 duplication identified in a large Chinese family with brachydactyly‐anonychia.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1392

By:

Liu, Mohan;
Zhang, Xueguang;
Liu, Hongqian;
Shen, Ying

Publication type:

Article

A 235 Kb deletion at 17q21.33 encompassing the COL1A1, and two additional secondary copy number variants in an infant with type I osteogenesis imperfecta: A rare case report.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 6, p. 1, doi. 10.1002/mgg3.1241

By:

Numbere, Numbereye;
Weber, David R.;
Porter, George;
Iqbal, Mohammed A.

Publication type:

Article

18q12.3‐q21.1 microdeletion detected in the prenatally alcohol‐exposed dizygotic twin with discordant fetal alcohol syndrome phenotype.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 4, p. 1, doi. 10.1002/mgg3.1192

By:

Kahila, Hanna;
Marjonen, Heidi;
Auvinen, Pauliina;
Avela, Kristiina;
Riikonen, Raili;
Kaminen‐Ahola, Nina

Publication type:

Article

A novel interstitial deletion of chromosome 2q21.1‐q23.3: Case report and literature review.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 4, p. 1, doi. 10.1002/mgg3.1135

By:

Almuzzaini, Bader;
Alatwi, Nasser S.;
Alsaif, Saif;
Al Balwi, Mohammed A.

Publication type:

Article