about
Splice variants of the relaxin and INSL3 receptors reveal unanticipated molecular complexityGonadotropin-releasing hormone agonists sensitize, and resensitize, prostate cancer cells to docetaxel in a p53-dependent mannerOrientation of amide-nitrogen-15 chemical shift tensors in peptides: a quantum chemical study.Telomere DNA deficiency is associated with development of human embryonic aneuploidyImproved sensitivity to detect recombination using qPCR for Dyskeratosis Congenita PGD.Powerful SNP-set analysis for case-control genome-wide association studies.Lack of association of KATNAL1 gene sequence variants and azoospermia in humansVariability of Gene Expression Identifies Transcriptional Regulators of Early Human Embryonic Development.Single embryo transfer with comprehensive chromosome screening results in improved ongoing pregnancy rates and decreased miscarriage rates.Massively Systematic Transcript End Readout, "MASTER": Transcription Start Site Selection, Transcriptional Slippage, and Transcript Yields.Interactions between RNA polymerase and the core recognition element are a determinant of transcription start site selectionRare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeGenetic polymorphisms of peptidase inhibitor 3 (elafin) are associated with acute respiratory distress syndrome.Genetic Mutation that May Contribute to Failure of Prolapse Surgery in White Women: A Case-Control Study.Next Generation Sequencing-Based Comprehensive Chromosome Screening in Mouse Polar Bodies, Oocytes, and Embryos.Identification and characterization of Aurora kinase B and C variants associated with maternal aneuploidy.Trophectoderm DNA fingerprinting by quantitative real-time PCR successfully distinguishes sibling human embryosDevelopment and validation of an accurate quantitative real-time polymerase chain reaction-based assay for human blastocyst comprehensive chromosomal aneuploidy screening.Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.Antiinflammatory effects of aprepitant coadministration with cART regimen containing ritonavir in HIV-infected adults.Dual targeting of tumor and endothelial cells by gonadotropin-releasing hormone agonists to reduce melanoma angiogenesis.In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial.Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease.Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial.Uniparental disomy in the human blastocyst is exceedingly rare.Comparative expression analysis of four breast cancer subtypes versus matched normal tissue from the same patients.Clinically recognizable error rate after the transfer of comprehensive chromosomal screened euploid embryos is low.Rare copy number variants in patients with congenital conotruncal heart defects.GSA-Genie: a web application for gene set analysispathVar: a new method for pathway-based interpretation of gene expression variabilityCharacterizing the uterine microbiome: next generation sequencing of the V4 region of the 16S ribosomal geneHigh cellularity of trophectoderm biopsy adversely affects pregnancy outcomesThe accuracy of blastocoel fluid comprehensive chromosomal screening (CCS) is dependent on amplification yield and sequencing depth when using nextgen sequencingUse of whole genome sequencing to identify chromosome-specific egg aneuploidy in a mouse model of natural reproductive agingCreation of a DNA bank from patients with infertility: a powerful resource for advancing the biology of reproductionDetection of contamination by quantitative real-time (q)PCRDevelopment and validation of a next-generation sequencing (NGS)-based 24-chromosome aneuploidy screening systemDevelopment of a SNP array based methodology for mouse single cell comprehensive chromosomal aneuploidy screeningTagging SNP genotyping and targeted next-generation sequencing of the katnal gene to investigate a putative genetic association with azoospermiaTargeted deep sequencing of maternal cohesin genes as putative biomarkers for increased risk of embryonic aneuploidy
P50
Q28264243-D81C837D-1982-467D-A75C-92F7F75C471CQ28537723-5D1D8DAE-1F7C-43EE-891F-FC6D2BC89201Q30328402-4981C05E-10BA-4143-9220-1511A16093F3Q33954500-DC9AF800-641F-4C33-ACF4-DC16E4A4934DQ34145752-A87B8197-C8B2-406F-BFA9-93627CE2F996Q34544433-9C9B69F8-85CB-40E4-A92A-AC1BFD023D55Q34662333-869B9BAB-1720-4795-8265-DB7651CC50D9Q35750406-50E778CF-0BB8-4F78-82B0-66073BBBC641Q35829512-2A2186E5-F5CD-4B6F-ACE3-F4E3111DAA44Q35857698-985A0C4C-9A0A-4ACC-BF77-6EBA40309571Q36012968-E66D5C52-97AA-435A-B30B-3C8F081E5FFEQ36977128-24FC2470-1FC6-400F-BF5C-35AC8B6F259CQ37443227-835ABB09-F6AA-4657-B962-EABBED1BEFFDQ38395196-1E722C1A-2E7E-41A0-9910-BF2BA9A83A63Q38791368-D0DD178D-2851-4D6E-8432-C6D44E376EAFQ38860108-A43E658C-8A69-4F4D-BBD2-3AC1F58CD743Q38965376-59A30EE6-1BD9-4791-A11C-C04B1A270FFFQ39395214-FEFE8358-3C7F-449B-8137-4FCBC0D6429CQ40216740-2CFA0406-85E0-43E6-9E02-0372D01CED56Q41924104-67B9893B-E634-4C1F-8AB5-E03A9AFCDCECQ42946229-1725FF56-6511-48A3-8BDA-63732410D549Q44232985-759A344B-CD5B-4F2D-A37F-43C00BCE2EB6Q45802005-DC59A3D8-2D64-4AD7-A603-2A238F342E3EQ48623792-B04A566C-5E7D-4CAE-9D97-CB7A9C9431ABQ48924750-F5A21AEA-EEF1-453A-8031-9C349CC4B5BDQ53482509-A889B5D7-1F5C-4BF2-8C92-EB007ABC960DQ54183255-DFC50B2F-7F40-4287-88AC-EF12654CF1E5Q55003862-5B5E34BC-6BD4-4922-82D2-FC5BA67B63C0Q58011290-368B5D1B-49C6-40C7-A96E-6D40D1A16117Q58011301-78B0DA6A-25B4-4A1F-8880-5FFDD77CE1A2Q58011326-8A213F18-A49A-4BBD-9BD1-FC5AD0466B3DQ58011332-82BAF449-BEB2-4B09-A7B1-B1FC5A6B96A7Q58011335-9CEF9E8C-5AE1-41DB-B6E6-97AF22F87C22Q58011340-3AE5B471-1BC1-4057-839A-8BF9F2FA320AQ58011354-2E60FCB1-2877-461D-B06E-FB40EBEB0DE8Q58011357-F4222F8B-E19A-4E2A-8A9E-239084C9E65CQ58011361-26794BCB-AF72-4634-9ADB-2E770968B90AQ58011366-D5CC7C0B-0360-488E-BA97-D6D404FE6829Q58011371-FB0D9580-1F2D-4C5D-922F-A87ECB4198D2Q58011373-379F2CCB-D65C-4A68-9B01-197B7831FA69
P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
@hy
name
Deanne M. Taylor
@ast
Deanne M. Taylor
@en
Deanne M. Taylor
@es
Deanne M. Taylor
@nl
Deanne M. Taylor
@sl
type
label
Deanne M. Taylor
@ast
Deanne M. Taylor
@en
Deanne M. Taylor
@es
Deanne M. Taylor
@nl
Deanne M. Taylor
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prefLabel
Deanne M. Taylor
@ast
Deanne M. Taylor
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Deanne M. Taylor
@es
Deanne M. Taylor
@nl
Deanne M. Taylor
@sl
P1053
Q-4777-2017
P106
P1153
55475226700
P21
P31
P3829
P496
0000-0002-3302-4610