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SMC1A wt Allele

Known as: KIAA0178, Structural Maintenance of Chromosomes 1A wt Allele, Smcb 
Human SMC1A wild-type allele is located within Xp11.22-p11.21 and is approximately 49 kb in length. This allele, which encodes Structural Maintenance… 
National Institutes of Health

Related topics

Related topics

4 relations
Cell Cycle ControlMitosisStructural Maintenance of Chromosomes Protein 1AXp11.22-p11.21

Papers overview

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2016
2016
Analisis Kebangkrutan dengan Menggunakan Metode Altman Z-score Springate dan Zmijewski pada Perusahaan Semen yang Terdaftar di BEI Periode 2011-2015
Bankruptcy is a condition which is avoided by the entire company. One way to avoid bankruptcy is to identify it early or as soon… 
2014
2014
OPTIMALISASI PORTOFOLIO MENGGUNAKAN CAPITAL ASSET PRICING MODEL (CAPM) DAN MEAN VARIANCE EFFICIENT PORTFOLIO (MVEP) (Studi Kasus: Saham-Saham LQ45)
Investment is planting some funds to get profit. However, there is a positive relationship between risk and return that is High… 
2010
2010
Upbeat and Quirky, With a Bit of a Build: Communicating Meaning and Meeting Information Needs in the Music Industry
Music is widely used to accompany moving images, in films, advertising, television programmes and computer games. The process of… 
2009
2009
Analysis on Selective Function of SMCB in National Standard
The definition and characteristics of SMCB in the national standard were introduced and the emphasis was paid on the selective… 
2008
2008
Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes
Cornelia de Lange syndrome (CdLS) is a rare, multiple congenital anomaly/mental retardation syndrome characterized by varied… 
Highly Cited
2007
Highly Cited
2007
Incidence and clinical features of X‐linked Cornelia de Lange syndrome due to SMC1L1 mutations
Cornelia de Lange syndrome (CdLS) is a multisystem developmental disorder characterized by facial dysmorphism, growth and mental… 
2007
2007
Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients
Cornelia de Lange syndrome (CdLS; OMIM 122470) is a rare multiple congenital anomaly/mental retardation syndrome characterized by… 
2007
2007
Packet Switching and Replication of Multicast Traffic by Crosspoint Buffered Packet Switches
Multicast traffic is expected to increase in packet-oriented networks by the inclusion of broadcast and multimedia-on-demand… 
Highly Cited
1996
Highly Cited
1996
Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
To test the centromere misdivision model of isochromosome formation, we have defined the breakpoints of cytogenetically… 
1986
1986
Crevettes de la famille des Pandalidae récoltées durant ces dernières années en Polynésie française Description de Plesionika chacei et P. carsini spp. nov
— Trap fishing in French Polynesia, at Mururoa (Tuamotu Archipelago), Tubuai (Austral Islands), and Tahiti obtained twelve… 
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