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SET-NUP214 fusion in acute myeloid leukemia- and T-cell acute lymphoblastic leukemia-derived cell lines

Author(s): Quentmeier Hilmar | Schneider Björn | Röhrs Sonja | Romani Julia | Zaborski Margarete | MacLeod Roderick | Drexler Hans
Serological and Molecular Typing of Plum pox Virus Isolates in the Transylvania, Romania

Author(s): Ioan ZAGRAI | Luminita ZAGRAI | Beatrix FERENCZ | Ioana PETRICELE | Doru PAMFIL | Octavian POPESCU | Alexandru BRICIU | Angela FESTILA
X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation

Author(s): Ferreira Susana | Matoso Eunice | Pinto Marta | Almeida Joana | Liehr Thomas | Melo Joana | Carreira Isabel
Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions

Author(s): Uddin Raihan | Zhang Yang | Siu Victoria | Fan Yao-Shan | O'Reilly Richard | Rao Jay | Singh Shiva
WCDMA Multiservice Uplink Capacity of Highways Cigar-Shaped Microcells

Author(s): Bazil Taha-Ahmed | Miguel Calvo Ramon
Precise detection of rearrangement breakpoints in mammalian chromosomes

Author(s): Lemaitre Claire | Tannier Eric | Gautier Christian | Sagot Marie-France
Comparative genome mapping of the deer mouse (Peromyscus maniculatus) reveals greater similarity to rat (Rattus norvegicus) than to the lab mouse (Mus musculus)

Author(s): Ramsdell Clifton | Lewandowski Adrienne | Glenn Julie | Vrana Paul | O'Neill Rachel | Dewey Michael
Partial duplication of the PRLR and SPEF2 genes at the late feathering locus in chicken

Author(s): Elferink Martin | Vallée Amélie | Jungerius Annemieke | Crooijmans Richard | Groenen Martien
Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report

Author(s): Murthy Sabita | Malhotra Ashok | Jacob Preenu | Naveed Sehba | Al-Rowaished Eman | Mani Sara | Padariyakam Shabeer | Pramathan R | Nath Ravi | Al-Ali Mahmoud | Al-Gazali Lihadh
TFIP11, CCNL1 and EWSR1 Protein-protein Interactions, and Their Nuclear Localization

Author(s): Sissada Tannukit | Xin Wen | HongJun Wang | Michael L. Paine
High-resolution array CGH clarifies events occurring on 8p in carcinogenesis

Author(s): Cooke Susanna | Pole Jessica | Chin Suet-Feung | Ellis Ian | Caldas Carlos | Edwards Paul
ComPhy: prokaryotic composite distance phylogenies inferred from whole-genome gene sets

Author(s): Lin Guan | Cai Zhipeng | Lin Guohui | Chakraborty Sounak | Xu Dong
Chromosomal plasticity and evolutionary potential in the malaria vector Anopheles gambiae sensu stricto: insights from three decades of rare paracentric inversions

Author(s): Pombi Marco | Caputo Beniamino | Simard Frederic | Di Deco Maria | Coluzzi Mario | Torre Alessandra | Costantini Carlo | Besansky Nora | Petrarca Vincenzo
Distal Xq duplication and functional Xq disomy

Author(s): Sanlaville Damien | Schluth-Bolard Caroline | Turleau Catherine
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation

Author(s): Auber Bernd | Bruemmer Verena | Zoll Barbara | Burfeind Peter | Boehm Detlef | Liehr Thomas | Brockmann Knut | Wilichowski Ekkehard | Argyriou Loukas | Bartels Iris
Bayesian DNA copy number analysis

Author(s): Rancoita Paola | Hutter Marcus | Bertoni Francesco | Kwee Ivo
Jacobsen syndrome

Author(s): Mattina Teresa | Perrotta Concetta | Grossfeld Paul
Gene synteny comparisons between different vertebrates provide new insights into breakage and fusion events during mammalian karyotype evolution

Author(s): Kemkemer Claus | Kohn Matthias | Cooper David | Froenicke Lutz | Högel Josef | Hameister Horst | Kehrer-Sawatzki Hildegard
A mitotic recombination map proximal to the APC locus on chromosome 5q and assessment of influences on colorectal cancer risk

Author(s): Howarth Kimberley | Ranta Susanna | Winter Eitan | Teixeira Ana | Schaschl Helmut | Harvey John | Rowan Andrew | Jones Angela | Spain Sarah | Clark Susan | Guenther Thomas | Stewart Aengus | Silver Andrew | Tomlinson Ian
The mitochondrial genome structure of Xenoturbella bocki (phylum Xenoturbellida) is ancestral within the deuterostomes

Author(s): Bourlat Sarah | Rota-Stabelli Omar | Lanfear Robert | Telford Maximilian
Most parsimonious haplotype allele sharing determination

Author(s): Cai Zhipeng | Sabaa Hadi | Wang Yining | Goebel Randy | Wang Zhiquan | Xu Jiaofen | Stothard Paul | Lin Guohui
Multichromosomal median and halving problems under different genomic distances

Author(s): Tannier Eric | Zheng Chunfang | Sankoff David
Distinct retroelement classes define evolutionary breakpoints demarcating sites of evolutionary novelty

Author(s): Longo Mark | Carone Dawn | Green Eric | O'Neill Michael | O'Neill Rachel
Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 → qter) detected in an autistic boy

Author(s): Carreira Isabel | Melo Joana | Rodrigues Carlos | Backx Liesbeth | Vermeesch Joris | Weise Anja | Kosyakova Nadezda | Oliveira Guiomar | Matoso Eunice
Analysis of fine-scale mammalian evolutionary breakpoints provides new insight into their relation to genome organisation

Author(s): Lemaitre Claire | Zaghloul Lamia | Sagot Marie-France | Gautier Christian | Arneodo Alain | Tannier Eric | Audit Benjamin
Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?

Author(s): Lissoni Sara | Baronchelli Simona | Villa Nicoletta | Lucchini Valeria | Betri Enrico | Cavalli Pietro | Dalprà Leda
Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities

Author(s): Katayama Kentaro | Miyamoto Sayaka | Furuno Aki | Akiyama Kouyou | Takahashi Sakino | Suzuki Hiroetsu | Tsuji Takehito | Kunieda Tetsuo
Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2

Author(s): Bernard Veronica | Minnerop Martina | Bürk Katrin | Kreuz Friedmar | Gillessen-Kaesbach Gabriele | Zühlke Christine
Long-range regulation is a major driving force in maintaining genome integrity

Author(s): Mongin Emmanuel | Dewar Ken | Blanchette Mathieu
A balanced t(5;17) (p15;q22-23) in chondroblastoma: frequency of the re-arrangement and analysis of the candidate genes

Author(s): Romeo Salvatore | Szuhai Karoly | Nishimori Isao | Ijszenga Marije | Wijers-Koster Pauline | Taminiau Antonie | Hogendoorn Pancras
Genomic aberrations in borderline ovarian tumors

Author(s): Micci Francesca | Haugom Lisbeth | Ahlquist Terje | Andersen Hege | Abeler Vera | Davidson Ben | Trope Claes | Lothe Ragnhild | Heim Sverre
Whole-genome sequencing of a laboratory-evolved yeast strain

Author(s): Araya Carlos | Payen Celia | Dunham Maitreya | Fields Stanley
Characterization and frequency of a newly identified HIV-1 BF1 intersubtype circulating recombinant form in São Paulo, Brazil

Author(s): Sanabani Sabri | de Souza Pastena Évelyn | Neto Walter | Martinez Vanessa | Sabino Ester
The role of recombination in the emergence of a complex and dynamic HIV epidemic

Author(s): Zhang Ming | Foley Brian | Schultz Anne-Kathrin | Macke Jennifer | Bulla Ingo | Stanke Mario | Morgenstern Burkhard | Korber Bette | Leitner Thomas
Reconstructing genome trees of prokaryotes using overlapping genes

Author(s): Cheng Chih-Hsien | Yang Chung-Han | Chiu Hsien-Tai | Lu Chin Lung
Exploring the 7p22.1 Chromosome as a Candidate Region for Autism

Author(s): Nadia Bayou | Ahlem Belhadj | Hussein Daoud | Sylvain Briault | M. Bechir Helayem | Habiba Chaabouni | Ridha M'rad
Non random distribution of genomic features in breakpoint regions involved in chronic myeloid leukemia cases with variant t(9;22) or additional chromosomal rearrangements

Author(s): Albano Francesco | Anelli Luisa | Zagaria Antonella | Coccaro Nicoletta | Casieri Paola | Rossi Antonella | Vicari Laura | Liso Vincenzo | Rocchi Mariano | Specchia Giorgina
Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation

Author(s): Wu Ye | Ji Taoyun | Wang Jingmin | Xiao Jing | Wang Huifang | Li Jie | Gao Zhijie | Yang Yanling | Cai Bin | Wang Liwen | Zhou Zhongshu | Tian Lili | Wang Xiaozhu | Zhong Nan | Qin Jiong | Wu Xiru | Jiang Yuwu
Genomic characterization of large rearrangements of the LDLR gene in Czech patients with familial hypercholesterolemia

Author(s): Goldmann Radan | Tichý Lukáš | Freiberger Tomáš | Zapletalová Petra | Letocha Ondřej | Soška Vladimír | Fajkus Jiří | Fajkusová Lenka
Novel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiency

Author(s): Coeli Fernanda | Soardi Fernanda | Bernardi Renan | de Araújo Marcela | Paulino Luciana | Lau Ivy | Petroli Reginaldo | de Lemos-Marini Sofia | Baptista Maria | Guerra-Júnior Gil | de-Mello Maricilda
Viral replication is enhanced by an HIV-1 intersubtype recombination-derived Vpu protein

Author(s): De Candia Cristian | Espada Constanza | Duette Gabriel | Ghiglione Yanina | Turk Gabriela | Salomón Horacio | Carobene Mauricio
A novel spliced fusion of MLL with CT45A2 in a pediatric biphenotypic acute leukemia

Author(s): Cerveira Nuno | Meyer Claus | Santos Joana | Torres Lurdes | Lisboa Susana | Pinheiro Manuela | Bizarro Susana | Correia Cecília | Norton Lucília | Marschalek Rolf | Teixeira Manuel
Phosphorylation of HOX11/TLX1 on Threonine-247 during mitosis modulates expression of cyclin B1

Author(s): Chen Edwin | Huang Xiaoyong | Zheng Yanzhen | Li You-Jun | Chesney Alden | Ben-David Yaacov | Yang Eric | Hough Margaret
Prenatal diagnosis and molecular cytogenetic analysis of a de novo isodicentric chromosome 18

Author(s): Zhang Yanliang | Dai Yong | Ren Jinghui | Wang Linqian
Breakpoint structure of the Anopheles gambiae 2Rb chromosomal inversion

Author(s): Lobo Neil | Sangaré Djibril | Regier Allison | Reidenbach Kyanne | Bretz David | Sharakhova Maria | Emrich Scott | Traore Sekou | Costantini Carlo | Besansky Nora | Collins Frank
Debugging, Advanced Debugging and Runtime Analysis

Author(s): Salim Istyaq | Aufaq Zargar
Bcr is a substrate for Transglutaminase 2 cross-linking activity

Author(s): Yi Sun-Ju | Groffen John | Heisterkamp Nora
Enrichment of intersubtype HIV-1 recombinants in a dual infection system using HIV-1 strain-specific siRNAs

Author(s): Gao Yong | Abreha Measho | Nelson Kenneth | Baird Heather | Dudley Dawn | Abraha Awet | Arts Eric
Developing high throughput genotyped chromosome segment substitution lines based on population whole-genome re-sequencing in rice (Oryza sativa L.)

Author(s): Xu Jianjun | Zhao Qiang | Du Peina | Xu Chenwu | Wang Baohe | Feng Qi | Liu Qiaoquan | Tang Shuzhu | Gu Minghong | Han Bin | Liang Guohua
Tyrosine kinase inhibitors: Multi-targeted or single-targeted?

Author(s): Fleur Broekman | Elisa Giovannetti | Godefridus J Peters
Diagnostic value of cancer-testis antigen mRNA in peripheral blood from hepatocellular carcinoma patients

Author(s): Li Zhao, Dong-Cheng Mou, Ji-Run Peng, Lei Huang, Zeng-An Wu, Xi-Sheng Leng
PTPRF is disrupted in a patient with syndromic amastia

Author(s): Ausavarat Surasawadee | Tongkobpetch Siraprapa | Praphanphoj Verayuth | Mahatumarat Charan | Rojvachiranonda Nond | Snabboon Thiti | Markello Thomas | Gahl William | Suphapeetiporn Kanya | Shotelersuk Vorasuk
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene

Author(s): Ghahramani Seno Mohammad | Kwan Benjamin | Lee-Ng Ka Ki | Moessner Rainald | Lionel Anath | Marshall Christian | Scherer Stephen
Fusion of the NUP98 gene with the LEDGF/p52 gene defines a recurrent acute myeloid leukemia translocation

Author(s): Hussey Damian | Moore Sarah | Nicola Mario | Dobrovic Alexander
Computer aided analysis of additional chromosome aberrations in Philadelphia chromosome positive acute lymphoblastic leukaemia using a simplified computer readable cytogenetic notation

Author(s): Bradtke Jutta | Balz Harald | Fonatsch Christa | Heinze Barbara | Jauch Anna | Mohr Brigitte | Schoch Claudia | Rieder Harald
Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AI1 viral integration site to 14q13.3-q21.1

Author(s): Gough Sheryl | McDonald Margaret | Chen Xiao-Ning | Korenberg Julie | Neri Antonino | Kahn Tomas | Eccles Michael | Morris Christine
Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

Author(s): Belogianni Ioulia | Apessos Angela | Mihalatos Markos | Razi Evangelia | Labropoulos Stefanos | Petounis Andreas | Gaki Vasiliki | Keramopoulos Antonios | Pandis Nikos | Kyriacou Kyriacos | Hadjisavvas Andreas | Kosmidis Paris | Yannoukakos Drakoulis | Nasioulas Georgios
Real-time PCR quantitation of glucocorticoid receptor alpha isoform

Author(s): Melo Murilo | Faria Cláudia | Melo Keli | Rebouças Nancy | Longui Carlos
CGHPRO – A comprehensive data analysis tool for array CGH

Author(s): Chen Wei | Erdogan Fikret | Ropers H-Hilger | Lenzner Steffen | Ullmann Reinhard
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome

Author(s): Schüle Birgitt | Albalwi Mohammed | Northrop Emma | Francis David | Rowell Margaret | Slater Howard | Gardner RJ McKinlay | Francke Uta
RESPIRATORY RATE IS A VALID AND RELIABLE MARKER FOR THE ANAEROBIC THRESHOLD: IMPLICATIONS FOR MEASURING CHANGE IN FITNESS

Author(s): Daniel G. Carey | Leslie A. Schwarz | German J. Pliego | Robert L. Raymond
Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes

Author(s): Stefan Mihaela | Claiborn Kathryn | Stasiek Edyta | Chai Jing-Hua | Ohta Tohru | Longnecker Richard | Greally John | Nicholls Robert
Comparison of chromosomal and array-based comparative genomic hybridization for the detection of genomic imbalances in primary prostate carcinomas

Author(s): Ribeiro Franclim | Henrique Rui | Hektoen Merete | Berg Marianne | Jerónimo Carmen | Teixeira Manuel | Lothe Ragnhild
High-resolution comparative mapping among man, cattle and mouse suggests a role for repeat sequences in mammalian genome evolution

Author(s): Schibler Laurent | Roig Anne | Mahe Marie-Françoise | Laurent Pascal | Hayes Hélène | Rodolphe François | Cribiu Edmond
BCR and its mutants, the reciprocal t(9;22)-associated ABL/BCR fusion proteins, differentially regulate the cytoskeleton and cell motility

Author(s): Zheng Xiaomin | Güller Saskia | Beissert Tim | Puccetti Elena | Ruthardt Martin
Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications

Author(s): Torres-Juan Laura | Rosell Jordi | Sánchez-de-la-Torre Manuel | Fibla Joan | Heine-Suñer Damià
High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic

Author(s): Vasickova Petra | Machackova Eva | Lukesova Miroslava | Damborsky Jiri | Horky Ondrej | Pavlu Hana | Kuklova Jitka | Kosinova Veronika | Navratilova Marie | Foretova Lenka
Phylogenomics of species from four genera of New World monkeys by flow sorting and reciprocal chromosome painting

Author(s): Dumas Francesca | Stanyon Roscoe | Sineo Luca | Stone Gary | Bigoni Francesca
A high resolution radiation hybrid map of bovine chromosome 14 identifies scaffold rearrangement in the latest bovine assembly

Author(s): Marques Elisa | de Givry Simon | Stothard Paul | Murdoch Brenda | Wang Zhiquan | Womack James | Moore Stephen
Gene expression profiling reveals different pathways related to Abl and other genes that cooperate with c-Myc in a model of plasma cell neoplasia

Author(s): Park Eun Sung | Shaughnessy John | Gupta Shalu | Wang Hongyang | Lee Ju-Seog | Woo Hyun Goo | Zhan Fenghuang | Owens James | Potter Michael | Janz Siegfried | Mushinski J Frederic
PCR-based karyotyping of Anopheles gambiae inversion 2Rj identifies the BAMAKO chromosomal form

Author(s): Coulibaly Mamadou | Pombi Marco | Caputo Beniamino | Nwakanma Davis | Jawara Musa | Konate Lassana | Dia Ibrahima | Fofana Abdrahamane | Kern Marcia | Simard Frédéric | Conway David | Petrarca Vincenzo | Torre Alessandra | Traoré Sékou | Besansky Nora
Functional annotation of 19,841 Populus nigra full-length enriched cDNA clones

Author(s): Nanjo Tokihiko | Sakurai Tetsuya | Totoki Yasushi | Toyoda Atsushi | Nishiguchi Mitsuru | Kado Tomoyuki | Igasaki Tomohiro | Futamura Norihiro | Seki Motoaki | Sakaki Yoshiyuki | Shinozaki Kazuo | Shinohara Kenji
Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region

Author(s): Jiang Yong-hui | Wauki Kekio | Liu Qian | Bressler Jan | Pan Yanzhen | Kashork Catherine | Shaffer Lisa | Beaudet Arthur
Chromosomal assignment of canine THADA gene to CFA 10q25

Author(s): Soller Jan | Beuing Claudia | Escobar Hugo | Winkler Susanne | Reimann-Berg Nicola | Drieschner Norbert | Dolf Gaudenz | Schelling Claude | Nolte Ingo | Bullerdiek Jörn
Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature

Author(s): Vorsanova Svetlana | Iourov Ivan | Voinova-Ulas Victoria | Weise Anja | Monakhov Victor | Kolotii Alexei | Soloviev Ilia | Novikov Petr | Yurov Yuri | Liehr Thomas
The Creatine Transporter Gene Paralogous at 16p11.2 Is Expressed in Human Brain

Author(s): Nadia Bayou | Ridha M'rad | Ahlem Belhaj | Hussein Daoud | Ramzi Zemni | Sylvain Briault | M. Béchir Helayem | Lamia Ben Jemaa | Habiba Chaabouni
FISH mapping of Philadelphia negative BCR/ABL1 positive CML

Author(s): Virgili Anna | Brazma Diana | Reid Alistair | Howard-Reeves Julie | Valgañón Mikel | Chanalaris Anastasios | De Melo Valeria | Marin David | Apperley Jane | Grace Colin | Nacheva Ellie
Breakpoint Tuning in DCT-Based Nonlinear Layered Video Codecs

Author(s): Antonio Garrido | Francisco Delicado | Luis Orozco-Barbosa | Pedro Cuenca
Antifungal susceptibility testing ? available methods and interpretative difficulties

Author(s): Małgorzata Prażyńska | Eugenia Gospodarek | Emilia Ciok-Pater
In Vitro Activities of Nine Current Antibiotics against Culprit Bacteria in Nosocomial Infections in an Institution in Northern Taiwan

Author(s): Sai-Cheong Lee | Shie-Shian Huang | Lai-Chu See | Ming-Han Tsai | Wen-Ben Shieh
MOLECULAR PATHOGENESIS OF SECONDARY ACUTE PROMYELOCYTIC LEUKEMIA

Author(s): Melanie Joannides | Ashley N Mays | Anita R Mistry | Syed Khizer Hasan | Andreas Reiter | Joseph L Wiemels | Carolyn A Felix | Francesco Lo-Coco | Neil Osheroff | Ellen Solomon | David Grimwade
Benchmarking homogenization algorithms for monthly data

Author(s): V. K. C. Venema | O. Mestre | E. Aguilar | I. Auer | J. A. Guijarro | P. Domonkos | G. Vertacnik | T. Szentimrey | P. Stepanek | P. Zahradnicek | J. Viarre | G. Müller-Westermeier | M. Lakatos | C. N. Williams | M. J. Menne | R. Lindau | D. Rasol | E. Rustemeier | K. Kolokythas | T. Marinova | L. Andresen | F. Acquaotta | S. Fratianni | S. Cheval | M. Klancar | M. Brunetti | C. Gruber | M. Prohom Duran | T. Likso | P. Esteban | T. Brandsma
ENERGY EFFICIENCY. TRENDS AND INFLUENCE FACTORS

Author(s): Gheorghe ZAMAN | Zizi GOSCHIN
Association study between schizophrenia and the DISC1 gene polymorphism

Author(s): Ali Mohammad Foroughmand | Maryam Haidari | Hamid Galehdari | Atefeh Pooryasin | Seyed Reza Kazeminejad | Shiva Hosseini | Nahid Khajeh-Mogehi
The rise and fall of breakpoint reuse depending on genome resolution

Author(s): Attie Oliver | Darling Aaron | Yancopoulos Sophia
Genome dedoubling by DCJ and reversal

Author(s): Thomas Antoine | Varré Jean-Stéphane | Ouangraoua Aïda
DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation

Author(s): Kato Takema | Inagaki Hidehito | Tong Maoqing | Kogo Hiroshi | Ohye Tamae | Yamada Kouji | Tsutsumi Makiko | Emanuel Beverly | Kurahashi Hiroki
Breakpoint characterization of a novel large intragenic deletion of MUTYH detected in a MAP patient: Case report

Author(s): Torrezan Giovana | da Silva Felipe | Krepischi Ana | Santos Érika | de O Ferreira Fábio | Rossi Benedito | Carraro Dirce
Breakpoint Tuning in DCT-Based Nonlinear Layered Video Codecs

Author(s): Cuenca Pedro | Orozco-Barbosa Luis | Delicado Francisco | Garrido Antonio
Is thermospheric long-term cooling due to CO2 or O3?

Author(s): P. L. Walsh | W. L. Oliver
Recombination in Hepatitis C Virus

Author(s): Fernando González-Candelas | F. Xavier López-Labrador | María Alma Bracho
Benchmarking monthly homogenization algorithms

Author(s): V. K. C. Venema | O. Mestre | E. Aguilar | I. Auer | J. A. Guijarro | P. Domonkos | G. Vertacnik | T. Szentimrey | P. Stepanek | P. Zahradnicek | J. Viarre | G. Müller-Westermeier | M. Lakatos | C. N. Williams | M. Menne | R. Lindau | D. Rasol | E. Rustemeier | K. Kolokythas | T. Marinova | L. Andresen | F. Acquaotta | S. Fratianni | S. Cheval | M. Klancar | M. Brunetti | C. Gruber | M. Prohom Duran | T. Likso | P. Esteban | T. Brandsma
Breakpoint characterization of large deletions in EXT1 or EXT2 in 10 Multiple Osteochondromas families

Author(s): Jennes Ivy | de Jong Danielle | Mees Kirsten | Hogendoorn Pancras | Szuhai Karoly | Wuyts Wim
Accurate and exact CNV identification from targeted high-throughput sequence data

Author(s): Nord Alex | Lee Ming | King Mary-Claire | Walsh Tom
Arm-specific dynamics of chromosome evolution in malaria mosquitoes

Author(s): Sharakhova Maria | Xia Ai | Leman Scotland | Sharakhov Igor
A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability

Author(s): Khan Muzammil | Rafiq Muhammad | Noor Abdul | Ali Nadir | Ali Ghazanfar | Vincent John | Ansar Muhammad
Sequence characteristics of T4-like bacteriophage IME08 genome termini revealed by high throughput sequencing

Author(s): Jiang Xiaofang | Jiang Huanhuan | Li Cun | Wang Sheng | Mi Zhiqiang | An Xiaoping | Chen Jiankui | Tong Yigang
Detection of recurrent rearrangement breakpoints from copy number data

Author(s): Ritz Anna | Paris Pamela | Ittmann Michael | Collins Colin | Raphael Benjamin
Close 3D proximity of evolutionary breakpoints argues for the notion of spatial synteny

Author(s): Véron Amélie | Lemaitre Claire | Gautier Christian | Lacroix Vincent | Sagot Marie-France
Delineating Chromosomal Breakpoints in Radiation-Induced Papillary Thyroid Cancer

Author(s): Heinz-Ulrich G. Weier | Yuko Ito | Johnson Kwan | Jan Smida | Jingly F. Weier | Ludwig Hieber | Chun-Mei Lu | Lars Lehmann | Mei Wang | Haig J. Kassabian | Hui Zeng | Benjamin O’Brien
Genomic imbalances in esophageal carcinoma cell lines involve Wnt pathway genes

Author(s): Jacqueline Brown | Hannelie Bothma | Robin Veale | Pascale Willem
WCDMA Multiservice Uplink Capacity of Highways Cigar-Shaped Microcells

Author(s): Taha-Ahmed Bazil | Ramon MiguelCalvo
Effect of plasticizer, pH and hydration on the mechanical and barrier properties of zein and ethylcellulose films

Author(s): C.A. Romero Bastida | M.O. Martin Polo | G. Velazquez | J.A. Torres
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