Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes - Wikidata - awgldk - TriplyDB

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

http://www.wikidata.org/entity/Q33927713

about

Aneuploidy: cells losing their balance Dissecting Alzheimer disease in Down syndrome using mouse models Mouse models of Down syndrome as a tool to unravel the causes of mental disabilities Dosage compensation is less effective in birds than in mammals Mechanisms of x chromosome dosage compensation.Genetically enhanced asynapsis of autosomal chromatin promotes transcriptional dysregulation and meiotic failure Chromosomal rearrangement interferes with meiotic X chromosome inactivation.The power of comparative and developmental studies for mouse models of Down syndrome Regional differences in dosage compensation on the chicken Z chromosome.Insights into the manifestations, outcomes, and mechanisms of leukemogenesis in Down syndrome Generation of a Mouse Full-length Balancer with Versatile Cassette-shuttling Selection Strategy.Aneuploidy: from a physiological mechanism of variance to Down syndrome.New insights into the troubles of aneuploidy Is it possible to improve neurodevelopmental abnormalities in Down syndrome?Gene copy-number alterations: a cost-benefit analysis.Trans-acting epigenetic effects of chromosomal aneuploidies: lessons from Down syndrome and mouse models.Enhanced apoptosis during early neuronal differentiation in mouse ES cells with autosomal imbalance.Genes and Small RNA Transcripts Exhibit Dosage-Dependent Expression Pattern in Maize Copy-Number Alterations.Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses.Dosage compensation of an aneuploid genome in mouse spermatogenic cells.

P2860

Q24654413-E8F6FF40-42EE-4FFF-BDF8-A75D5818C565 Q26777254-67486FA1-8091-42E2-A23D-0118C9F037A0 Q26863005-858B7115-892E-4A84-9DA7-440E5290396D Q28292598-8DE56AA5-9990-4B58-B502-4E9F180022BE Q35002469-EFB0356E-CD03-42CD-B7F4-BD9056EF06C0 Q35678395-97D5CF44-789F-4B88-93A0-ABAA8E476BE7 Q36004650-A4038F82-BC65-4DCF-ACE2-0553F4567AA9 Q36021399-73ED9958-5334-4A60-840F-2711C9673B0E Q36643321-C3F5B853-39EF-44E1-9C7C-76078D119987 Q37142140-16995D42-F5EB-410F-8649-DB60977D9786 Q37148542-FB190D5D-550D-4887-A500-3DFCB57DDB71 Q37543845-B451518D-B729-4E94-B5B7-B8FAF65909D6 Q37574324-9EA9CCC0-6B73-44B8-AC6A-FF7852F89903 Q37912174-216DEE34-EC46-4B17-ADF9-6A9B0E90B8F0 Q38078490-76DA0C73-CBF1-45A3-9054-B7A54754FF2B Q39027010-868D3A88-2E88-4724-B323-BCBFBAB6A3B9 Q39915424-4795C531-9375-40A2-9083-38CD59C4F3E7 Q41986489-536E118F-17EF-4552-9ECC-29E41C1A1E58 Q48126436-68B32B8D-9EB9-44DF-AAE5-14FFD4EEEA22 Q53053884-FA7E0854-8762-4CA4-B968-B855127BE5C8

P2860

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

http://www.wikidata.org/entity/Q33927713

description

2005 nî lūn-bûn

@nan

2005 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի մարտին հրատարակված գիտական հոդված

@hy

2005年の論文

@ja

2005年論文

@yue

2005年論文

@zh-hant

2005年論文

@zh-hk

2005年論文

@zh-mo

2005年論文

@zh-tw

2005年论文

@wuu

name

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

@ast

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

@en

type

label

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

@ast

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

@en

prefLabel

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

@ast

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

@en

P1433

Q33927713-36FF9C2C-EE94-4A7F-9531-7A9121ABC1F6

P1476

Q33927713-D98FF55D-A52A-4DFF-8D76-6EA8F744C9DE

P2093

Q33927713-5A257BDB-6B91-4AFE-9FBC-6F20A3149DCD

Q33927713-821FE00E-2FA8-46BD-96B7-5FA5D0C3E8BB

Q33927713-A17AE601-7A45-4AB4-8CCB-CBD69DB40681

Q33927713-C25BD2D7-DF60-4AB0-B23E-8F6C5A480ACF

Q33927713-C35FF91C-3835-4259-BEC6-7776033274E4

P2860

Q33927713-031A0B93-7955-4BBA-ABAD-95A94F45ADF6

Q33927713-08F659C9-CCF5-4EDE-94D7-78625BA02CD4

Q33927713-09A9E657-D0A8-44AD-81E2-AB79EB2A0318

Q33927713-0F67F49D-2625-4BD2-911C-710DC2F9E24B

Q33927713-1559FA35-5533-4944-A9E3-37BFD4BE332D

Q33927713-23AEAF2A-FF3E-4C70-8F2E-5CD12E02A074

Q33927713-2D85D0E3-95B5-4A10-BF14-8DBC1F2B126C

Q33927713-3212F5AA-7724-4E88-8713-2D020E8B3CCF

Q33927713-4FE0FCB8-2316-469B-BF2D-149FE932F4D9

Q33927713-50FA1206-5563-4559-8557-CB4A7D3DA508

P304

Q33927713-924E498F-D023-44D1-A374-631AD7E950ED

P31

Q33927713-881D51E8-B21B-4381-8FF8-65AED8397350

P356

Q33927713-BE7A7C87-BC27-487C-B0FE-6EF501D8CBDD

P407

Q33927713-EC59ED7C-46B0-4EC6-BC1F-73FD8889656F

P433

Q33927713-B53296F5-C52D-4BF7-83BA-5B4DBA6D5857

P478

Q33927713-FE583F21-F8CE-4D53-B680-92BF34D82F59

P50

Q33927713-64A803BB-CD1D-4BDC-8F28-9A11323E50BC

Q33927713-7C325ED2-E696-43D6-AC1F-84CD0B10F0A8

Q33927713-AC90C108-D7D2-4F1A-B98D-A84275E25A56

Q33927713-D70B75F9-BB0E-4A98-86CF-221535593B90

P577

Q33927713-2778B1C5-D0D6-44A9-A36D-F696D3C7161C

P5875

Q33927713-4202F9C3-25B7-426E-8B24-2CF83F81D9DA

P698

Q33927713-44C7A032-5966-4DEB-BDC3-80167C84FFC4

P932

Q33927713-31C43BA0-B953-4D72-96CA-E69319DF8284

P356

PNAS.0500802102

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes

@en

P2093

Allan Bradley

http://www.w3.org/2001/XMLSchema#string

Jan Bures

http://www.w3.org/2001/XMLSchema#string

Michael Ort

http://www.w3.org/2001/XMLSchema#string

Radek Blatny

http://www.w3.org/2001/XMLSchema#string

Sona Gregorová

http://www.w3.org/2001/XMLSchema#string

P2860

The DNA sequence of human chromosome 21

Global up-regulation of chromosome 21 gene expression in the developing Down syndrome brain

Chromosome 21 and down syndrome: from genomics to pathophysiology

Recent segmental duplications in the human genome

A whole-genome mouse BAC microarray with 1-Mb resolution for analysis of DNA copy number changes by array comparative genomic hybridization.

A chromosome 21 critical region does not cause specific Down syndrome phenotypes.

The "gene dosage effect" hypothesis versus the "amplified developmental instability" hypothesis in Down syndrome.

PWD/Ph and PWK/Ph inbred mouse strains of Mus m. musculus subspecies--a valuable resource of phenotypic variations and genomic polymorphisms.

Too much of a good thing: mechanisms of gene action in Down syndrome.

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome

P304

4500-4505

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1073/PNAS.0500802102

http://www.w3.org/2001/XMLSchema#string

P407

P433

12

http://www.w3.org/2001/XMLSchema#string

P478

102

http://www.w3.org/2001/XMLSchema#string

P50

P577

2005-03-08T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

7978200

http://www.w3.org/2001/XMLSchema#string

P698

15755806

http://www.w3.org/2001/XMLSchema#string

P932

552979

http://www.w3.org/2001/XMLSchema#string