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Showing 1 to 12 of 342 entries
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Support for the Diagnosis of CHARGE Syndrome-Reply.

JAMA otolaryngology-- head & neck surgery

Hirose K, Shinawi M.
PMID: 28241177
JAMA Otolaryngol Head Neck Surg. 2017 Jun 01;143(6):635. doi: 10.1001/jamaoto.2016.4765.

No abstract available.

Note of clarification of data in the paper titled X-ray repair cross-complementing group 1 codon 399 polymorphism and lung cancer risk: an updated meta-analysis.

Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine

Zhai W, Feng R, Wang H, Wang Y.
PMID: 25835974
Tumour Biol. 2015 May;36(5):3179-89. doi: 10.1007/s13277-015-3384-4. Epub 2015 Apr 03.

We read with great interest the paper titled "X-ray repair cross-complementing group 1 codon 399 polymorphism and lung cancer risk: an updated meta-analysis" published by Wang et al in Tumor Biology, 2014, 35:411-418. Their results suggest that codon 399...

What a 'Ku'incidence!: parallel discoveries of a new DNA repair factor.

Cell death and differentiation

Mistrik M, Bartek J.
PMID: 25941165
Cell Death Differ. 2015 Jun;22(6):888-9. doi: 10.1038/cdd.2015.32.

No abstract available.

Computational analysis of protein-DNA interactions from ChIP-seq data.

Methods in molecular biology (Clifton, N.J.)

Rougemont J, Naef F.
PMID: 21938632
Methods Mol Biol. 2012;786:263-73. doi: 10.1007/978-1-61779-292-2_16.

Chromatin immunoprecipitation experiments followed by ultra-high-throughput sequencing (ChIP-seq) is becoming the method of choice to identify transcription factor binding sites in prokaryotes and eukaryotes in vivo. Here, we review the computational steps that are necessary for analyzing the sequenced...

Neuroimaging in frontotemporal lobar degeneration--predicting molecular pathology.

Nature reviews. Neurology

Whitwell JL, Josephs KA.
PMID: 22290573
Nat Rev Neurol. 2012 Jan 31;8(3):131-42. doi: 10.1038/nrneurol.2012.7.

Frontotemporal lobar degeneration (FTLD) encompasses a group of diseases characterized by neuronal loss and gliosis of the frontal and temporal lobes. Almost all cases of FTLD can be classified into three categories on the basis of deposition of one...

Teaching case 3-2019: Are nuclear clefts or invaginations the niche of intranuclear inclusions in FTLD-TDP?.

Clinical neuropathology

Molina-Porcel L, Pérez-Navarro E, García-Forn M, Westaway D, Colom-Cadena M, Gelpi E.
PMID: 31023421
Clin Neuropathol. 2019 May/Jun;38(3):97-99. doi: 10.5414/NP301202.

No abstract available.

Editorial: Single-molecule studies of DNA-protein interactions collection 2021.

Nucleic acids research

Bianco PR, Sale JE, Reyes-Lamothe R.
PMID: 34153108
Nucleic Acids Res. 2021 Jun 21;49(11):6005-6006. doi: 10.1093/nar/gkab497.

No abstract available.

'Screw-cap' clamp loader proteins that thread.

Nature structural & molecular biology

Zhuang Z, Spiering MM, Berdis AJ, Trakselis MA, Benkovic SJ.
PMID: 15221017
Nat Struct Mol Biol. 2004 Jul;11(7):580-1. doi: 10.1038/nsmb0704-580.

No abstract available.

Crystallization of single-strand DNA-binding protein.

Journal of molecular biology

Monzingo AF, Christiansen C.
PMID: 6355489
J Mol Biol. 1983 Nov 05;170(3):801. doi: 10.1016/s0022-2836(83)80135-1.

No abstract available.

Note of clarification of data in the paper titled X-ray repair cross-complementing group 1 Arg194Trp polymorphism is associated with increased risk of lung cancer in Chinese Han population.

Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine

Yang H, Feng R, Wang H, Wang Y.
PMID: 25669171
Tumour Biol. 2015 Apr;36(4):2229-33. doi: 10.1007/s13277-015-3201-0. Epub 2015 Feb 11.

No abstract available.

An end to 40 years of mistakes in DNA-protein association kinetics?.

Biochemical Society transactions

Halford SE.
PMID: 19290859
Biochem Soc Trans. 2009 Apr;37:343-8. doi: 10.1042/BST0370343.

Proteins that bind to specific sequences in long DNA molecules have to locate their target sites amid myriad alternative sequences, yet they do so at remarkably rapid rates, sometimes approaching 10(10) M(-1) x s(-1). Hence, it has been asserted...

Impact of XRCC2 Arg188His polymorphism on cancer susceptibility: a meta-analysis.

PloS one

He Y, Zhang Y, Jin C, Deng X, Wei M, Wu Q, Yang T, Zhou Y, Wang Z.
PMID: 24621646
PLoS One. 2014 Mar 12;9(3):e91202. doi: 10.1371/journal.pone.0091202. eCollection 2014.

BACKGROUND: Association between the single nucleotide polymorphism rs3218536 (known as Arg188His) located in the X-ray repair cross complementing group 2 (XRCC2) gene and cancer susceptibility has been widely investigated. However, results thus far have remained controversial. A meta-analysis was...

Showing 1 to 12 of 342 entries