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Ts1Cje mouse model for Down syndrome research

Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics of Down syndrome (DS) individuals. To varying extent, DS individuals also exhibit other developmental problems such as heart defects, vision impairments, hearing loss, hypothyroidism, dental problems...

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Sonraí Bibleagrafaíochta
Príomhúdar:	Ling, King Hwa
Formáid:	Conference or Workshop Item
Teanga:	English
Foilsithe:	2015
Rochtain Ar Líne:	http://psasir.upm.edu.my/id/eprint/75610/1/Ts1Cje%20mouse%20model%20for%20Down%20syndrome%20research.pdf
Clibeanna:	Cuir Clib Leis Gan Chlibeanna, Bí ar an gcéad duine leis an taifead seo a chlibeáil!

Míreanna Comhchosúla

Transcriptional profiling of the postnatal brain of the Ts1Cje mouse model of Down syndrome
le: Tan, Kai Leng, et al.
Foilsithe: (2014)

The role of JAK-STAT signalling in the developing brain of Ts1Cje mouse model for Down syndrome
le: Lee, Han Chung, et al.
Foilsithe: (2015)

Expression profiling of genes involved in the development and function of skeletal muscles in Ts1Cje mouse model of down syndrome
le: Cheah, Pike See, et al.
Foilsithe: (2018)

Gene network disruptions and neurogenesis defects in the adult Ts1Cje mouse model of Down syndrome
le: Hewitt, Chelsee Ann, et al.
Foilsithe: (2010)

Histological and molecular characterisation of hypotonia in adult Ts1Cje mouse model for down syndrome /
le: Bala, Usman
Foilsithe: (2016)

Histological and molecular characterisation of hypotonia in adult Ts1Cje mouse model for down syndrome
le: Bala, Usman
Foilsithe: (2016)

Expression of gamma secretase and notch signallingpathway in TS1CJE mouse model of down syndrome /
le: Hadri Hadi Md Yusof,

Histological and molecular characterisation of hypotonia in adult Ts1Cje mouse model for down syndrome
le: Bala, Usman
Foilsithe: (2016)

Overexpression of interferon alpha or beta receptors in the brain of adult Ts1Cje mouse model of Down syndrome
le: Tan, Kai Leng, et al.
Foilsithe: (2015)

The expression profile of miR-3099 during neural development of Ts1Cje mouse model of down syndrome
le: Zainal Abidin, Shahidee, et al.
Foilsithe: (2021)

Perturbed metabolic profiles associated with muscle weakness seen in adult Ts1Cje mouse model of Down syndrome
le: Lim, Chai Ling, et al.
Foilsithe: (2019)

Expression of gamma secretase and notch signalling pathway in TS1CJE mouse model of down syndrome
le: Md Yusof, Hadri Hadi
Foilsithe: (2017)

Targeted differential gene expression profiling of skeletal muscles isolated from Ts1Cje mouse model for Down syndrome
le: Leong, Melody Pui Yee, et al.
Foilsithe: (2015)

Ts1Cje mouse model for Down syndrome exhibits motor function deficit; the potential role of MRFS and peripheral nervous system
le: Bala, Usman, et al.
Foilsithe: (2015)

Expression profiling of notch signalling pathway and gamma-secretase activity in the brain of Ts1Cje mouse model of down syndrome
le: Md Yusof, Hadri Hadi, et al.
Foilsithe: (2019)

Disrupted interferon-related molecular networks and the over-expressed Ifnar1 in the brain of adult Ts1Cje mouse model of Down syndrome
le: Tan, Kai Leng, et al.
Foilsithe: (2016)

Transcriptomic and protein expression analyses of skeletal muscles isolated from Ts1cje mouse model for Down syndrome /
le: Leong, Melody Pui Yee.
Foilsithe: (2017)

Identification of disrupted molecular networks involved in brain maturation and function in the TS1CJE mouse model of down syndrome /
le: Tan, Kai Leng.
Foilsithe: (2016)

Transcriptomic and protein expression analyses of skeletal muscles isolated from Ts1cje mouse model for Down syndrome
le: Leong, Melody Pui Yee
Foilsithe: (2017)

Identification of disrupted molecular networks involved in brain maturation and function in the TS1CJE mouse model of down syndrome
le: Tan, Kai Leng
Foilsithe: (2016)

Metabolic profiling of neurospheres derived from embryonic cerebral cortex Ts1Cje mouse model for down syndrome
le: Mohamed Seth, Eryse Amira
Foilsithe: (2019)

Metabolic profiling of neurospheres derived from embryonic cerebral cortex Ts1Cje mouse model for down syndrome /
le: Eryse Amira Mohamed Seth,

The identification of disrupted molecular networks involved in brain maturation and function in the Ts1Cje mouse model of down syndrome.
le: Cheah, P. S.

Transcriptomic and protein expression analyses of skeletal muscles isolated from Ts1cje mouse model for Down syndrome
le: Leong, Melody Pui Yee
Foilsithe: (2017)

Identification of disrupted molecular networks involved in brain maturation and function in the TS1CJE mouse model of down syndrome
le: Tan, Kai Leng
Foilsithe: (2016)

Metabolic profiling of neurospheres derived from embryonic cerebral cortex Ts1Cje mouse model for down syndrome
le: Mohamed Seth, Eryse Amira
Foilsithe: (2019)

Gene and protein expression profiles of JAK-STAT signalling pathway in the developing brain of the Ts1Cje down syndrome mouse model
le: Lee, Han Chung, et al.
Foilsithe: (2019)

Metabolic and functional characterisation of adult skeletal muscle in down syndrome mouse model (Ts1CJe) for insights into hypotonia in human condition /
le: Lim, Chai Ling.
Foilsithe: (2017)

Metabolic and functional characterisation of adult skeletal muscle in down syndrome mouse model (Ts1CJe) for insights into hypotonia in human condition
le: Lim, Chai Ling
Foilsithe: (2017)

Metabolic and functional characterisation of adult skeletal muscle in down syndrome mouse model (Ts1CJe) for insights into hypotonia in human condition
le: Lim, Chai Ling
Foilsithe: (2017)

Defects in nerve conduction velocity and different muscle fibre-type specificity contribute to muscle weakness in Ts1Cje Down syndrome mouse model
le: Bala, Usman, et al.
Foilsithe: (2018)

Functional transcriptome analysis of the postnatal brain of the Ts1Cje mouse model for Down syndrome reveals global disruption of interferon-related molecular networks
le: Ling, King Hwa, et al.
Foilsithe: (2014)

Down syndrome : a promising future, together /
Foilsithe: (1999)

Prenatal screening of down syndrome.
le: Rosli, Rozita, et al.
Foilsithe: (2006)

MicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID and Fragile X syndrome
le: Siew, Wei Hong, et al.
Foilsithe: (2013)

Adolescents with Down Syndrome : toward a more fulfilling life /
Foilsithe: (1997)

Exploring SOD1 gene for the detection of fetal Down syndrome
le: Karrupiah, Thilakavathy, et al.
Foilsithe: (2008)

Nutritional status of children with down syndrome at the Kiwanis Down Syndrome centres in Petaling Jaya and Seremban /
le: Shalini Muthu

Protein expression in down syndrome brain /
Foilsithe: (2001)

Improving the communication of people with down syndrome /
Foilsithe: (1999)