Analysis of CDK13-related disorder in a mouse model
CDK13-related disorder, a developmental syndrome associated with intellectual disability, facial dysmorphism, congenital heart defects, brain defects, and growth abnormalities, is a recently identified syndrome caused by mutations in the serine-threonine protein kinase CDK13. CDK13 is thought to pla...
| Main Author: | Abbad, Aseel |
|---|---|
| Format: | Thesis (University of Nottingham only) |
| Language: | English |
| Published: |
2024
|
| Subjects: | |
| Online Access: | https://eprints.nottingham.ac.uk/79950/ |
Similar Items
The prevalence and survival of children with congenital septal defects in the UK using CPRD
by: Onuwe, Toluwalope Yetunde
Published: (2022)
by: Onuwe, Toluwalope Yetunde
Published: (2022)
Genetic studies on congenital heart disorders
by: Aparicio Sánchez, José Juan
Published: (2020)
by: Aparicio Sánchez, José Juan
Published: (2020)
Homocysteine metabolism enzyme gene polymorphisms in non-syndromic Malaysian congenital heart disease patients
by: Mohamad, Nur Afiqah
Published: (2013)
by: Mohamad, Nur Afiqah
Published: (2013)
Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations
by: Granados-Riveron, Javier T., et al.
Published: (2012)
by: Granados-Riveron, Javier T., et al.
Published: (2012)
Elucidating the role of Cdk13 and Prkd1 in heart development and congenital heart disease
by: Waheed Ullah, Qazi
Published: (2024)
by: Waheed Ullah, Qazi
Published: (2024)
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
by: Sifrim, Alejandro, et al.
Published: (2016)
by: Sifrim, Alejandro, et al.
Published: (2016)
Dose reduction using care dose4d technique of siemens dual-source computed tomography on pediatric congenital heart disease
by: Chen, HongYing
Published: (2022)
by: Chen, HongYing
Published: (2022)
Dimensional Accuracy and Clinical Value of 3D Printed Models in Congenital Heart Disease: A Systematic Review and Meta-Analysis
by: Lau, Ivan, et al.
Published: (2019)
by: Lau, Ivan, et al.
Published: (2019)
Tropomyosin 1: multiple roles in the developing heart and in the formation of congenital heart defects
by: England, Jennifer, et al.
Published: (2017)
by: England, Jennifer, et al.
Published: (2017)
Identifying novel genes that cause congenital heart disease
by: Wilsdon, Anna
Published: (2021)
by: Wilsdon, Anna
Published: (2021)
Molecular profiling and combinatorial activity of CCT068127: a potent CDK2 and CDK9 inhibitor
by: Whittaker, Steven R., et al.
Published: (2018)
by: Whittaker, Steven R., et al.
Published: (2018)
Cardiac troponin T is necessary for normal development in the embryonic chick heart
by: England, Jennifer, et al.
Published: (2016)
by: England, Jennifer, et al.
Published: (2016)
Improved resolution and signal-to-noise ratio performance of a confocal fluorescence microscope
by: Kakade, Rohan
Published: (2016)
by: Kakade, Rohan
Published: (2016)
Novel Structural Features of CDK Inhibition Revealed by an ab Initio Computational MethodCombined with Dynamic Simulations
by: Heady, L., et al.
Published: (2006)
by: Heady, L., et al.
Published: (2006)
The effect of tightly-bound water molecules on scaffold diversity in computer-aided de novo ligand design of CDK2 inhibitors
by: Garcia-sosa, A., et al.
Published: (2006)
by: Garcia-sosa, A., et al.
Published: (2006)
N_LyST: a simple and rapid screening test for Lynch Syndrome
by: Susanti, Susanti, et al.
Published: (2018)
by: Susanti, Susanti, et al.
Published: (2018)
The relationship of CDK18 expression in breast cancer to clinicopathological parameters and therapeutic response
by: Barone, Giancarlo, et al.
Published: (2018)
by: Barone, Giancarlo, et al.
Published: (2018)
Segmenting the right ventricle cavity from 4D echocardiography images for stroke volume measurement
by: Abboud, Anas A.
Published: (2014)
by: Abboud, Anas A.
Published: (2014)
Hoxa9 collaborates with E2A-PBX1 in mouse B cell leukemia in association with Flt3 activation and decrease of B cell gene expression
by: Hassawi, Mona, et al.
Published: (2014)
by: Hassawi, Mona, et al.
Published: (2014)
Interrogating the genetic profile of sporadic colorectal cancer
by: Fadhil, Wakkas M.
Published: (2019)
by: Fadhil, Wakkas M.
Published: (2019)
GENE NETWORKS CONTROLLING ANTHER TAPETUM DEVELOPMENT IN BARLEY (Hordeum vulgare) DURING EARLY ANTHER DEVELOPMENT
by: HUA, Miaoyuan
Published: (2021)
by: HUA, Miaoyuan
Published: (2021)
SPACA3gene variants in a New Zealand cohort of infertile and fertile couples
by: Prendergast, Deborah, et al.
Published: (2014)
by: Prendergast, Deborah, et al.
Published: (2014)
Premenstrual syndrome and premenstrual dysphonic disorder
by: Khajehei, Marjan, et al.
Published: (2010)
by: Khajehei, Marjan, et al.
Published: (2010)
Understanding the pathogenesis and potential therapeutics of Myotonic dystrophy
by: Verma, Ayushri
Published: (2024)
by: Verma, Ayushri
Published: (2024)
The potential utility of stem cells in the treatment of congenital heart disease
by: Davies, Ben
Published: (2009)
by: Davies, Ben
Published: (2009)
Overlap of proteomics biomarkers between women with pre-eclampsia and PCOS: a systematic review and biomarker database integration
by: Khan, Gulafshana Hafeez, et al.
Published: (2014)
by: Khan, Gulafshana Hafeez, et al.
Published: (2014)
A draft genome sequences and molecular characterisation of glycoprotein B and lower matrix phosphoprotein of rat cytomegalovirus all-3 strain
by: Quah, Yi Wan
Published: (2013)
by: Quah, Yi Wan
Published: (2013)
Effectiveness of health education in improving knowledge and attitude towards toxoplasmosis among pregnant women in Al Najaf, Iraq
by: Ibadi, Atheer Kadhim
Published: (2016)
by: Ibadi, Atheer Kadhim
Published: (2016)
Relationships Between Stereotyped Movements and Sensory Processing Disorders in Children With and Without Developmental or Sensory Disorders
by: Gal, E., et al.
Published: (2010)
by: Gal, E., et al.
Published: (2010)
Identification of developmental coordination disorder in primary school aged Kuwaiti children
by: Alanzi, Suad Eid Farhan
Published: (2011)
by: Alanzi, Suad Eid Farhan
Published: (2011)
Personalized Three-Dimensional Printed Models in Congenital Heart Disease
by: Sun, Zhonghua, et al.
Published: (2019)
by: Sun, Zhonghua, et al.
Published: (2019)
Characteristics of auditory processing disorder in primary school-aged children
by: Ferguson, Melanie A.
Published: (2014)
by: Ferguson, Melanie A.
Published: (2014)
Analysis of sensitivity and resolution in plasmonic microscopes
by: Pechprasarn, Suejit
Published: (2012)
by: Pechprasarn, Suejit
Published: (2012)
Regression mouse mammary tumour through complement-mediated inflammation of C5A/C5AR axis
by: Kamarudin, Nurul Hazwani
Published: (2015)
by: Kamarudin, Nurul Hazwani
Published: (2015)
Production, Establishment and Characterisation of Monoclonal Antibody Against Breast Cancer Cell Line (Mcf-7)
by: Ong, Boo Kean
Published: (1995)
by: Ong, Boo Kean
Published: (1995)
Elucidating the role of MOZ and its implications for KAT6A Global Developmental Delay syndrome
by: Whitchurch, Jonathan B.
Published: (2019)
by: Whitchurch, Jonathan B.
Published: (2019)
"The problem with running" - Comparing the propulsion strategy of children with Developmental Coordination Disorder and typically developing children
by: Diamond, N., et al.
Published: (2014)
by: Diamond, N., et al.
Published: (2014)
Metabolic interactions between axons and Schwann cells of the mouse sciatic nerve
by: Rich, Laura
Published: (2022)
by: Rich, Laura
Published: (2022)
Brain transcriptome perturbations in the Hfe -/- mouse model of genetic iron loading
by: Johnstone, D., et al.
Published: (2012)
by: Johnstone, D., et al.
Published: (2012)
Exploring the potential to use data linkage for investigating the relationship between birth defects and prenatal alcohol exposure
by: O'Leary, Colleen Marie, et al.
Published: (2013)
by: O'Leary, Colleen Marie, et al.
Published: (2013)
Similar Items
-
The prevalence and survival of children with congenital septal defects in the UK using CPRD
by: Onuwe, Toluwalope Yetunde
Published: (2022) -
Genetic studies on congenital heart disorders
by: Aparicio Sánchez, José Juan
Published: (2020) -
Homocysteine metabolism enzyme gene polymorphisms in non-syndromic Malaysian congenital heart disease patients
by: Mohamad, Nur Afiqah
Published: (2013) -
Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations
by: Granados-Riveron, Javier T., et al.
Published: (2012) -
Elucidating the role of Cdk13 and Prkd1 in heart development and congenital heart disease
by: Waheed Ullah, Qazi
Published: (2024)