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*  Characterization of the effects of a 7 amino-acid delet | Open-i
Characterization of the effects of a 7 amino-acid deletion in p6gag to the HIV-1 proteins expression, release and maturation. ... Molecular Sequence Data. *Protein Structure, Tertiary. *Receptors, CCR5/metabolism. *Sequence Deletion. *Species Specificity ... It contains a 7 amino-acid deletion in its p6gag. We conducted a cohort study to compare viral loads and CD4 cell count changes ... An HIV-1-NL4-3 mutant virus which contains a 7 amino-acid deletion in p6gag (designated as 7d virus) was generated and its live ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC4263662_pone.0114441.g003&req=4
*  Defective Interfering Particles And Their Role In Disease Progression And Persistence
... are internal deletion mutants of viruses that replicate at the disbursement of the parent virus. This review article aim... ... Defective interfering particles (DIPs) are internal deletion mutants of viruses that replicate at the disbursement of the ... Fungal Genome Sequencing. *Fungal Hyphae. *Fungal Nail Infection. *Fungal Pathogens. *Gallbladder tuberculosis ...
  https://www.omicsonline.org/proceedings/defective-interfering-particles-and-their-role-in-disease-progression-and-persistence-65037.html
*  Replication error deficient and proficient colorectal cancer gene expression differences caused by 3'UTR polyT sequence...
Sequence analysis of the 3'UTRs of a selection of the most differentially expressed genes shows that they all contain deletions ... Analysis of the incidence of mononucleotide repeat sequences in the 3'UTRs, 5'UTRs, and coding sequences of those genes most ... are found in the 3'UTR sequence of most genes. The relevant sequences are typically A/U-rich elements or U repeats. Microarray ... These cancers are typically pseudodiploid, accumulate mutations in repetitive sequences as a result of their mismatch repair ...
  https://www.rdm.ox.ac.uk/publications/179140
*  CDH1 Sequencing and Deletion/Duplication - Quest Diagnostics Nichols Institute of Valencia
Sequencing and deletion/duplication analyses of the CDH1 gene will identify individuals at risk for CHD1-related cancers. ...
  http://www.specialtylabs.com/tests/details.asp?id=92568
*  Stk11 Sequencing And Deletion/duplication - Quest Diagnostics Nichols Institute of Valencia
Sequencing and deletion/duplication analyses of the STK11 gene will identify individuals who are affected with PJS and ...
  http://specialtylabs.com/tests/details.asp?id=92565
*  Ornithine Transcarbamylase Deficiency (OTC) Sequencing and Deletion/Duplication
Background Information for Ornithine Transcarbamylase Deficiency (OTC) Sequencing and Deletion/Duplication:. Characteristics: ... The breakpoints of large deletions/duplications will not be determined.. Compliance Statement C: For human genetic inheritable ... Methodology: Bidirectional sequencing of the entire coding region and intron-exon boundaries of the OTC gene. Multiplex ... Limitations: Diagnostic errors can occur due to rare sequence variations. Regulatory region mutations and deep intronic ...
  http://ltd.aruplab.com/Tests/Pub/2004896
*  Peutz-Jeghers Syndrome (STK11) Sequencing and Deletion/Duplication
Background Information for Peutz-Jeghers Syndrome (STK11) Sequencing and Deletion/Duplication. Characteristics: Hamartomatous ... Deletion/duplication breakpoints will not be determined. Compliance Statement C: For human genetic inheritable conditions and ... Methodology: Bidirectional sequencing and multiplex ligation-dependent probe amplification (MLPA) of the entire coding region ... 2008398 - Peutz-Jeghers Syndrome (STK11) Sequencing and Deletion/Duplication. http://ltd.aruplab.com/tests/pub/2008398 ...
  http://ltd.aruplab.com/Tests/Pub/2008398
*  Cobalamin/Propionate/Homocysteine Metabolism Related Disorders Panel, Sequencing and Deletion/Duplication
Genes Sequenced: ABCD4, ACSF3, AMN, CBS, CD320, CUBN, GIF, HCFC1, LMBRD1, MAT1A, MCEE, MMAA, MMAB, MMACHC, MMADHC, MTHFR, MTR, ... Genes Deletion/Duplication: ABCD4, ACSF3, AMN, CBS, CD320, CUBN, GIF, LMBRD1, MAT1A, MCEE, MMAA, MMAB, MMACHC, MMADHC, MTHFR, ... Genes Deletion/Duplication: ABCD4, ACSF3, AMN, CBS, CD320, CUBN, GIF, LMBRD1, MAT1A ... Genes Sequenced: ABCD4, ACSF3, AMN, CBS, CD320, CUBN, GIF, HCFC1, LMBRD1, MAT1A ...
  http://ltd.aruplab.com/tests/pub/2011157
*  Vascular Malformations Panel, Sequencing and Deletion/Duplication, 14 Genes
Sequencing and Deletion/Duplication. *2009326 Cerebral Cavernous Malformation (CCM) Panel, Sequencing and Deletion/Duplication ... 2001976 Juvenile Polyposis (SMAD4) Deletion/Duplication. *2002470 PTEN-Related Disorders (PTEN) Sequencing and Deletion/ ... 2003405 Pulmonary Arterial Hypertension (BMPR2) Sequencing and Deletion/Duplication. *2007852 RASA1-Related Disorders (RASA1) ... 0051382 Hereditary Hemorrhagic Telangiectasia (ACVRL1 and ENG) Sequencing and Deletion Duplication. *0051510 Juvenile Polyposis ...
  http://ltd.aruplab.com/Tests/Pub/2007384
*  Holoprosencephaly Panel, Nonsyndromic, Sequencing and Deletion/Duplication, 11 Genes, Fetal
2008863 - Holoprosencephaly Panel, Nonsyndromic, Sequencing and Deletion/Duplication, 11 Genes, Fetal. http://ltd.aruplab.com/ ...
  http://ltd.aruplab.com/Tests/Pub/2008863
*  21 New Sequencing and Deletion / Duplication Tests Added | Connective Tissue Gene Tests
March 5, 2015 - Connective Tissue Gene Tests (CTGT) is pleased to announce 21 new Sequencing and Deletion / Duplication tests. ...
  http://ctgt.net/news/21-new-sequencing-and-deletion-duplication-tests-added-0
*  Tay-Sachs Disease (HEXA) Sequencing and 7.6kb Deletion
Large deletions/duplications in HEXA, other than the 7.6kb deletion, will not be detected.. Compliance Statement C: For human ... Background for Tay-Sachs Disease (HEXA) Sequencing and 7.6kb Deletion:. Characteristics: Hexosaminidase A (HEX A) enzyme ... Methodology: Bidirectional sequencing of all coding regions and intron/exon boundaries of the HEXA gene. Agarose gel ... 2009298 - Tay-Sachs Disease (HEXA) Sequencing and 7.6kb Deletion. http://ltd.aruplab.com/tests/pub/2009298 ...
  http://ltd.aruplab.com/tests/pub/2009298
*  Nucleotide sequence and deletion analysis of the xylanase gene (xynZ) of Clostridium thermocellum. - CORE
Nucleotide sequence and deletion analysis of the xylanase gene (xynZ) of Clostridium thermocellum. By O Grépinet, M C Chebrou ... The nucleotide sequence of the xynZ gene, encoding the extracellular xylanase Z of Clostridium thermocellum, was determined. ... Deletions removing up to 508 codons from the 5' end of the gene did not affect the activity of the encoded polypeptide, showing ...
  https://core.ac.uk/display/3295781
*  Sequence Similarity - 1F0F: Cecropin A(1-8)-magainin 2(1-12) gig deletion modification in dodecylphosphocholine...
Structures of protein chains with identical sequences (sequence identity > 95%) are aligned, superimposed and clustered. ... Sequence Similarity Clusters for the Entities in PDB 1F0F Legend Entity #1 , Chains: A CECROPIN A-MAGAININ 2 HYBRID PEPTIDE ... Blast this sequence against all of PDB Archive.. Rank. In each cluster, the chains are sorted (i.e. ranked) according to the ... In the table for each entity, view a list of similar sequences by selecting the link associated with the percentage cutoff. ...
  http://www.rcsb.org/pdb/explore/sequenceCluster.do?structureId=1F0F
*  Infantile Epilepsy Panel, Sequence Analysis and Exon-Level Deletion/Duplication
Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map. ...
  http://ltd.aruplab.com/Tests/Pub/2007535
*  IDENTIFICATION AND CLINICAL ASSESSMENT OF DELETION STRUCTURAL VARIANTS IN WHOLE GENOME SEQUENCES OF ACUTELY ILL NEONATES
... ... Deletion structural variants (SVs) 50 nucleotides are implicated in many genetic diseases and with WGS data can now be ... Pipeline usage in 10 proband family sets revealed a possibly causative deletion SV in the MMP21 gene for two siblings. MMP21 is ... CONCLUSIONS The identification of deletion SVs has the potential to increase the diagnostic yield of WGS data. The methods ...
  https://kuscholarworks.ku.edu/handle/1808/14508
*  Fluorescence in situ hybridization analysis with LIST specific probes reveals a high deletion mutation rate in isolated...
We have analyzed patients with isolated lissencephaly sequence (ILS) by FISH with probes at D17S379, an anonymous locus distal ... Deletions were found in eight additional individuals.. Conclusion:. The overall deletion mutation rate detectable by FISH with ... In 110 patients with ILS, a deletion at D17S379 was detected in 23.6%. Of those patients without a deletion, 32 were available ... situ hybridization analysis with LIST specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence ...
  https://insights.ovid.com/gemed/199811000/00125817-199811000-00007
*  Five novel ZEB1 mutations including a 0.34 Mb deletion detected by whole genome sequencing in patients with posterior...
Five novel ZEB1 mutations including a 0.34 Mb deletion detected by whole genome sequencing in patients with posterior ... Five novel ZEB1 mutations including a 0.34 Mb deletion detected by whole genome sequencing in patients with posterior ... Methods : Ocular examination, Sanger sequencing of ZEB1 coding regions in all probands and whole genome sequencing in one ... Five novel ZEB1 mutations including a 0.34 Mb deletion detected by whole genome sequencing in patients with posterior ...
  https://iovs.arvojournals.org/article.aspx?articleid=2690899
*  Partial promoter substitutions generating transcriptional sentinels of diverse signaling pathways in embryonic stem cells and...
Rationale for Rosa26 promoter sequence deletion and replacement. Our approach was to partially delete the regulatory sequences ... 3000 bp deletion points noted above (Fig. 1D). The TA-CFP sequence was inserted at the −228 and −60 bp deletion points. ... By employing the constitutively active Rosa26 gene and analyzing its upstream promoter sequences, we made successive deletions ... The −228 deletion endpoint satisfied these criteria, whereas the −60 deletion retained high constitutive activity. Fortunately ...
  http://dmm.biologists.org/content/5/6/956
*  Ultrasensitive Detection of Chimerism by Single-Molecule Molecular Inversion Probe Capture and High-Throughput Sequencing of...
... of Chimerism by Single-Molecule Molecular Inversion Probe Capture and High-Throughput Sequencing of Copy Number Deletion ... of Chimerism by Single-Molecule Molecular Inversion Probe Capture and High-Throughput Sequencing of Copy Number Deletion ... of Chimerism by Single-Molecule Molecular Inversion Probe Capture and High-Throughput Sequencing of Copy Number Deletion ... Methods: We designed a 159-smMIP panel targeting 40 autosomal regions of frequent homozygous deletion across human populations ...
  http://clinchem.aaccjnls.org/content/early/2018/03/16/clinchem.2017.284737
*  Characterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markers | BMC Genomics | Full Text
The amplicon content of partial AZFc deletion products was characterized with novel amplicon-specific sequence markers. Data ... and although high diversity of partial deletion products and sequence conversion profiles were recorded, the AZFc marker ... Although partial AZFc deletion products are highly heterogeneous in terms of amplicon content, this plasticity is not ... Yet, partial AZFc deletions yield phenotypes ranging from normospermia to azoospermia, thwarting definite conclusions on their ...
  https://bmcgenomics.biomedcentral.com/articles/10.1186/1471-2164-8-342
*  Mutation services, Point mutations deletion mutations. 100% sequence guarantee - From Bioneer
Send us your sequence, gene ID or an accession number. Let us know what you need and we will deliver! Bioneer also offers ... purify and sequence your gene of interest. If you like, our free codon optimization will increase protein expression rates and ... In as little as 2 weeks, you can have your gene cloned in hand and 100% sequence guaranteed. And with Bioneer's great pricing ... Automatic DNA sequencer (ABI 3730) 를 이용한 100% sequence guarantee. Applications. Protein 기능 향상. 단백질의 3차구조를 기반으로 특정부위의 아미노산들을 ...
  http://www.bioneer.co.kr/products/GeneSynthesis/Mutagenesis-overview.aspx
*  RNA Therapeutics - & related info | Mendeley
Sequence Deletion. *Signal Transduction. *Signaling. *Squamous Cell. *Squamous Cell: genetics. *Stem Cell State ...
  https://www.mendeley.com/research-papers/rna-therapeutics-1/
*  Mutation Analysis of the THRA1 Gene in Breast Cancer: Deletion/Fusion of the Gene to a Novel Sequence on 17q in the BT474 Cell...
Mutation Analysis of the THRA1 Gene in Breast Cancer: Deletion/Fusion of the Gene to a Novel Sequence on 17q in the BT474 Cell ... Mutation Analysis of the THRA1 Gene in Breast Cancer: Deletion/Fusion of the Gene to a Novel Sequence on 17q in the BT474 Cell ... Mutation Analysis of the THRA1 Gene in Breast Cancer: Deletion/Fusion of the Gene to a Novel Sequence on 17q in the BT474 Cell ... Mutation Analysis of the THRA1 Gene in Breast Cancer: Deletion/Fusion of the Gene to a Novel Sequence on 17q in the BT474 Cell ...
  http://cancerres.aacrjournals.org/content/54/7/1791.long