Results 111 to 120 of about 638,215 (311)

Chromosomal Partners at Colinearity Breakpoints

, 2016
Chromosomal Partners at Colinearity ...
Asif Chinwalla (2189), Lucinda A Fulton (2196), Richard Durbin (2217), Robert E Fulton (2197), James C Mullikin (2207), David Willey (2215), Thomas Blumenthal (2186), Richard K Wilson (2216), Lincoln D Stein (2183), Michael R Brent (2187), Jacqueline E Schein (2210), Darin Blasiar (2185), John Spieth (2212), Jane Rogers (2209), Todd W Harris (2199), Robert H Waterston (1728), Tracie L Miner (2205), Peter D'Eustachio (2194), David H. A Fitch (2195), Sam Griffiths-Jones (2198), LaDeana W Hillier (2200), Ravi Kamath (2201), Marc Sohrmann (2211), Jason E Stajich (2213), Elaine R Mardis (2203), Robert W Plumb (2208), Alan Coulson (2193), Zhirong Bao (2184), Nansheng Chen (2188), Chaochun Wei (2214), Chris Clee (2191), Patrick Minx (2206), Laura Clarke (2190), Marco A Marra (2204), Avril Coghlan (2192), Patricia E Kuwabara (2202)   +35 more
core   +1 more source

Evolution‐guided yeast complementation reveals functional differences in human PSPH variants

FEBS Open Bio, EarlyView.
Ancient genomes can help guide which human genetic variants are tested experimentally. This study applies that idea to PSPH, a gene involved in serine biosynthesis, and uses high‐throughput yeast complementation to compare variant function. The findings reveal measurable differences among selected alleles and illustrate the value of evolution‐guided ...
Mauricio Campa‐Álvarez, Diana Ascencio, Miguel Vallebueno‐Estrada, Eduardo González‐Orozco, Christian Eduardo Martínez‐Guerrero, Rafael Montiel, Alexander DeLuna   +6 more
wiley   +1 more source

Identification of chromosomal abnormalities in miscarriages using single-nucleotide polymorphism arrays

Archives of Gynecology and Obstetrics
Purpose Chromosome abnormalities are a known cause of miscarriage. A detailed chromosomal study in miscarriages is delineated using high-throughput technologies.
Wantong Zhao, Haiwei Wang, Bin Liang, Hailong Huang, Na Lin, Liangpu Xu   +5 more
doaj   +1 more source

Dual native G‐quadruplex folding is associated with chromatin looping at the MYC locus

FEBS Open Bio, EarlyView.
BG4‐detectable G‐quadruplex (G4) in HaCaT and NHEK keratinocytes identified folded and unfolded G4s enriched at promoters/TSSs and active enhancers, whereas unfolded G4s also overlapped weak/poised enhancers. At MYC–PVT1, 3C‐qPCR detected enhancer–promoter looping only when G4s were simultaneously folded at both regulatory elements under native ...
Dieila Giomo de Lima, Gustavo Narvaes Guimarães, Emilyane de Oliveira Santana Amaral, Bianca Caroline Figueiredo Bianco, Manuel Jara‐Espejo, Sérgio Roberto Peres Line, Ana Paula de Souza, Aline Cristiane Planello   +7 more
wiley   +1 more source

Chromosomal Arms at Colinearity Breakpoints

, 2016
Chromosomal Arms at Colinearity ...
Asif Chinwalla (2189), Lucinda A Fulton (2196), Richard Durbin (2217), Robert E Fulton (2197), James C Mullikin (2207), David Willey (2215), Thomas Blumenthal (2186), Richard K Wilson (2216), Lincoln D Stein (2183), Michael R Brent (2187), Jacqueline E Schein (2210), Darin Blasiar (2185), John Spieth (2212), Jane Rogers (2209), Todd W Harris (2199), Robert H Waterston (1728), Tracie L Miner (2205), Peter D'Eustachio (2194), David H. A Fitch (2195), Sam Griffiths-Jones (2198), LaDeana W Hillier (2200), Ravi Kamath (2201), Marc Sohrmann (2211), Jason E Stajich (2213), Elaine R Mardis (2203), Robert W Plumb (2208), Alan Coulson (2193), Zhirong Bao (2184), Nansheng Chen (2188), Chaochun Wei (2214), Chris Clee (2191), Patrick Minx (2206), Laura Clarke (2190), Marco A Marra (2204), Avril Coghlan (2192), Patricia E Kuwabara (2202)   +35 more
core   +1 more source

Stochastic modelling of chromosomal segregation : errors can introduce correction [PDF]

, 2014
Cell division is a complex process requiring the cell to have many internal checks so that division may proceed and be completed correctly. Failure to divide correctly can have serious consequences, including progression to cancer.
Roitershtein, Alexander, Matzavinos, Anastasios, Voller, Zachary, Liu, Sijia, Shtylla, Blerta, Chaplain, Mark A.J., Chaplain, Mark A.J.; id_orcid   +6 more
core   +1 more source

Chromosomal microarray analysis in 1292 fetuses with ultrasound soft markers during mid-term pregnancy

The Journal of Maternal-Fetal & Neonatal Medicine
Background Soft markers found during mid-term pregnancy ultrasounds can indicate potential chromosomal abnormalities in fetuses. This study evaluates the association between ultrasound soft markers and chromosomal abnormalities, providing insights into ...
Xiaomei Yang, Li Sun, Yasong Xu, Shiyu Sun, Shoulan Zhou, Ping Lv   +5 more
doaj   +1 more source

Identification and characterisation of calcitonin receptor isoforms expressed in glioblastoma derived glioma stem and U‐87 MG cells

FEBS Open Bio, EarlyView.
Glioblastoma cells express calcitonin receptor variants (CT receptor isoforms) that may help them survive stress. Using qPCR, transcript‐specific long‐read nanopore sequencing, immunofluorescence co‐localisation and comparative sequence analysis, this study identifies a novel alternatively spliced CALCR transcript that encodes the CTb receptor isoform ...
Pragya Gupta, Sebastian GB Furness, Tahereh Gharbi, Ric De Paoli‐Iseppi, Shweta S. Joshi, Michael Clark, David L. Hare, Peter Wookey   +7 more
wiley   +1 more source

Chronic lymphocytic leukemia-associated chromosomal abnormalities and miRNA deregulation

, 2012
Yvonne Kiefer1, Christoph Schulte2, Markus Tiemann2, Joern Bullerdiek11Center for Human Genetics, University of Bremen, Bremen, Germany; 2Hematopathology Hamburg, Hamburg, GermanyAbstract: Chronic lymphocytic leukemia is the most common leukemia in ...
Bullerdiek J, Schulte C, Kiefer Y, Tiemann M   +3 more
core  

Newly mapped chromosomal loci of Neurospora crassa. [PDF]

, 1987
Newly mapped chromosomal loci of Neurospora ...
Pollard, V. C., V. C. Pollard, D. D. Perkins, Perkins, D. D.   +3 more
core   +1 more source