Cargando…

The Molecular Effects of a Polymorphism in the 5′UTR of Solute Carrier Family 44, Member 5 that Is Associated with Birth Weight in Holsteins

Dystocia is a major problem for the dairy cattle industry, and the observed high rates of this condition stem from genetic selection to increase subsequent milk production of the calving female. Because smaller birth size does not adversely affect subsequent milk production, selecting for cows with...

Descripción completa

Detalles Bibliográficos
Autores principales:	Sugimoto, Mayumi, Watanabe, Toshio, Sugimoto, Yoshikazu
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399839/ https://www.ncbi.nlm.nih.gov/pubmed/22815983 http://dx.doi.org/10.1371/journal.pone.0041267

Ejemplares similares

Molecular Effects of Polymorphism in the 3’UTR of Unc-5 homolog C Associated with Conception Rate in Holsteins
por: Sugimoto, Mayumi, et al.
Publicado: (2015)

Variant in the 5′ Untranslated Region of Insulin-Like Growth Factor 1 Receptor Is Associated With Susceptibility to Mastitis in Cattle
por: Sugimoto, Mayumi, et al.
Publicado: (2012)

Variants in the 3' UTR of General Transcription Factor IIF, polypeptide 2 affect female calving efficiency in Japanese Black cattle
por: Sasaki, Shinji, et al.
Publicado: (2013)

A missense mutation in solute carrier family 12, member 1 (SLC12A1) causes hydrallantois in Japanese Black cattle
por: Sasaki, Shinji, et al.
Publicado: (2016)

Genome-wide identification of copy number variation using high-density single-nucleotide polymorphism array in Japanese Black cattle
por: Sasaki, Shinji, et al.
Publicado: (2016)

Mapping and Exome Sequencing Identifies a Mutation in the IARS Gene as the Cause of Hereditary Perinatal Weak Calf Syndrome
por: Hirano, Takashi, et al.
Publicado: (2013)

Association between 5’-UTR and 3’-UTR Polymorphisms of the TYMS Gene and Breast Cancer in Kurdish Women of Iraq
por: Mohamad, Kazhal Shekh
Publicado: (2021)

Effects of prenatal heat stress on birth weight and birth weight genetic parameters in German Holstein calves
por: Yin, T., et al.
Publicado: (2023)

Functional polymorphism in the 5′-UTR of CR2 is associated with susceptibility to nasopharyngeal carcinoma
por: FAN, QIN, et al.
Publicado: (2013)

Complexity of the 5′UTR region of the CLCN5 gene: eleven 5′UTR ends are differentially expressed in the human kidney
por: Tosetto, Enrica, et al.
Publicado: (2014)

Prepubertal growth and single nucleotide polymorphism analysis of the growth hormone gene of low birth weight Holstein calves
por: Ro, Younghye, et al.
Publicado: (2018)

Genetic polymorphism of Pit-1 and CSN3 genes in Holstein calves and its associations with calf birth weight
por: Fındık, Ismail, et al.
Publicado: (2022)

Maternal Primary Carnitine Deficiency and a Novel Solute Carrier Family 22 Member 5 (SLC22A5) Mutation
por: Jakoby, Michael, et al.
Publicado: (2021)

DEFB1 gene 5′ untranslated region (UTR) polymorphisms in inflammatory bowel diseases
por: Zanin, Valentina, et al.
Publicado: (2012)

Effects of single nucleotide polymorphism marker density on degree of genetic variance explained and genomic evaluation for carcass traits in Japanese Black beef cattle
por: Ogawa, Shinichiro, et al.
Publicado: (2014)

A common polymorphism in the 5′ UTR of ERCC5 creates an upstream ORF that confers resistance to platinum-based chemotherapy
por: Somers, Joanna, et al.
Publicado: (2015)

Ionotropic Glutamate Receptor AMPA 1 Is Associated with Ovulation Rate
por: Sugimoto, Mayumi, et al.
Publicado: (2010)

Cross-breed comparisons identified a critical 591-kb region for bovine carcass weight QTL (CW-2) on chromosome 6 and the Ile-442-Met substitution in NCAPG as a positional candidate
por: Setoguchi, Kouji, et al.
Publicado: (2009)

Association of the solute carrier family 11 member 1 gene polymorphisms with susceptibility to leprosy in a Brazilian sample
por: Brochado, Maria José Franco, et al.
Publicado: (2016)

High expression of Solute Carrier Family 1, member 5 (SLC1A5) is associated with poor prognosis in clear-cell renal cell carcinoma
por: Liu, Yidong, et al.
Publicado: (2015)

Lack of Evidence of the Role of APOA5 3’UTR Polymorphisms in Iranian Children and Adolescents with Metabolic Syndrome
por: Salehi, Samaneh, et al.
Publicado: (2018)

A Functional 5'-UTR Polymorphism of MYC Contributes to Nasopharyngeal Carcinoma Susceptibility and Chemoradiotherapy Induced Toxicities
por: Guo, Zhen, et al.
Publicado: (2019)

5′-UTR and 3′-UTR Regulation of MICB Expression in Human Cancer Cells by Novel microRNAs
por: Wongfieng, Wipaporn, et al.
Publicado: (2017)

Impact of QTL minor allele frequency on genomic evaluation using real genotype data and simulated phenotypes in Japanese Black cattle
por: Uemoto, Yoshinobu, et al.
Publicado: (2015)

Evolution of alternative and constitutive regions of mammalian 5'UTRs
por: Resch, Alissa M, et al.
Publicado: (2009)

Before It Gets Started: Regulating Translation at the 5′ UTR
por: Araujo, Patricia R., et al.
Publicado: (2012)

Repression-free utrophin-A 5’UTR variants
por: Malik, Debasish, et al.
Publicado: (2019)

The Functional Meaning of 5′UTR in Protein-Coding Genes
por: Ryczek, Natalia, et al.
Publicado: (2023)

Significant associations between 5-hydroxytryptaminetransporter-linked promoter region polymorphisms of the serotonin transporter (solute carrier family 6 member 4) gene and Thai patients with autism spectrum disorder
por: Wongpaiboonwattana, Wikrom, et al.
Publicado: (2020)

Structural Lability in Stem–Loop 1 Drives a 5′ UTR–3′ UTR Interaction in Coronavirus Replication
por: Li, Lichun, et al.
Publicado: (2008)

Association between polymorphisms of thymidylate synthase gene 5′- and 3′-UTR and gastric cancer risk: meta-analysis
por: Mo, Ao, et al.
Publicado: (2016)

An integrated bioinformatic investigation of mitochondrial solute carrier family 25 (SLC25) in colon cancer followed by preliminary validation of member 5 (SLC25A5) in tumorigenesis
por: Chen, Yan-Jie, et al.
Publicado: (2022)

Identification and Characterization of a Splicing Variant in the 5′ UTR of the Human TLR5 Gene
por: Hoang, Thi Xoan, et al.
Publicado: (2017)

Influence of the 5′-terminal sequences on the 5′-UTR structure of HIV-1 genomic RNA
por: Obayashi, Camille Michiko, et al.
Publicado: (2021)

Effect of 5'UTR introns on gene expression in Arabidopsis thaliana
por: Chung, Betty YW, et al.
Publicado: (2006)

Cap-independent translation through the p27 5′-UTR
por: Jiang, Hong, et al.
Publicado: (2007)

5′-UTR RNA G-quadruplexes: translation regulation and targeting
por: Bugaut, Anthony, et al.
Publicado: (2012)

5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasia
por: Damjanovich, Kristy, et al.
Publicado: (2011)

5′-UTR G-quadruplex structures acting as translational repressors
por: Beaudoin, Jean-Denis, et al.
Publicado: (2010)

Secondary structure of the SARS-CoV-2 5’-UTR
por: Miao, Zhichao, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_p93djuu0e16l8qr6a24niodt9q