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Search results 1 to 21 out of 21 for Sept5

Category restricted to Publication

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Publication

17224448 | J:120894

First Author:	Taniguchi M
Year:	2007
Journal:	J Biol Chem
Title:	Phosphorylation of adult type Sept5 (CDCrel-1) by cyclin-dependent kinase 5 inhibits interaction with syntaxin-1.
Volume:	282
Issue:	11
Pages:	7869-76

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Publication

18385322 | -

First Author:	Amin ND
Year:	2008
Journal:	J Neurosci
Title:	Cyclin-dependent kinase 5 phosphorylation of human septin SEPT5 (hCDCrel-1) modulates exocytosis.
Volume:	28
Issue:	14
Pages:	3631-43

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Publication

10321247 | -

First Author:	Beites CL
Year:	1999
Journal:	Nat Neurosci
Title:	The septin CDCrel-1 binds syntaxin and inhibits exocytosis.
Volume:	2
Issue:	5
Pages:	434-9

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Publication

16767699 | -

First Author:	Bläser S
Year:	2006
Journal:	J Pathol
Title:	Human endothelial cell septins: SEPT11 is an interaction partner of SEPT5.
Volume:	210
Issue:	1
Pages:	103-10

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Publication

773946 | -

First Author:	Byers B
Year:	1976
Journal:	J Cell Biol
Title:	A highly ordered ring of membrane-associated filaments in budding yeast.
Volume:	69
Issue:	3
Pages:	717-21

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Publication

22314400 | -

First Author:	Mostowy S
Year:	2012
Journal:	Nat Rev Mol Cell Biol
Title:	Septins: the fourth component of the cytoskeleton.
Volume:	13
Issue:	3
Pages:	183-94

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Publication

21990096 | -

First Author:	Hall PA
Year:	2012
Journal:	J Pathol
Title:	Mammalian septins: dynamic heteromers with roles in cellular morphogenesis and compartmentalization.
Volume:	226
Issue:	2
Pages:	287-99

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Publication

24469395 | -

First Author:	Zhai G
Year:	2014
Journal:	Mol Cell Biol
Title:	Sept6 is required for ciliogenesis in Kupffer's vesicle, the pronephros, and the neural tube during early embryonic development.
Volume:	34
Issue:	7
Pages:	1310-21

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Publication

4950437 | -

First Author:	Hartwell LH
Year:	1971
Journal:	Exp Cell Res
Title:	Genetic control of the cell division cycle in yeast. IV. Genes controlling bud emergence and cytokinesis.
Volume:	69
Issue:	2
Pages:	265-76

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Publication

19240081 | J:147200

First Author:	Suzuki G
Year:	2009
Journal:	Hum Mol Genet
Title:	Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice.
Volume:	18
Issue:	9
Pages:	1652-60

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Publication

22589251 | J:185360

First Author:	Harper KM
Year:	2012
Journal:	Hum Mol Genet
Title:	Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain.
Volume:	21
Issue:	15
Pages:	3489-99

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Publication

17564677 | J:122593

First Author:	Fujishima K
Year:	2007
Journal:	J Neurochem
Title:	Targeted disruption of Sept3, a heteromeric assembly partner of Sept5 and Sept7 in axons, has no effect on developing CNS neurons.
Volume:	102
Issue:	1
Pages:	77-92

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Publication

22575789 | J:186260

First Author:	Yoshida A
Year:	2012
Journal:	Hear Res
Title:	Localization of septin proteins in the mouse cochlea.
Volume:	289
Issue:	1-2
Pages:	40-51

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Publication

18809578 | J:142823

First Author:	Tsang CW
Year:	2008
Journal:	Mol Cell Biol
Title:	Superfluous role of mammalian septins 3 and 5 in neuronal development and synaptic transmission.
Volume:	28
Issue:	23
Pages:	7012-29

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Publication

15213102 | J:93756

First Author:	Kato K
Year:	2004
Journal:	Blood
Title:	Genetic deletion of mouse platelet glycoprotein Ibbeta produces a Bernard-Soulier phenotype with increased alpha-granule size.
Volume:	104
Issue:	8
Pages:	2339-44

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Publication

15355307 | J:116266

First Author:	Beites CL
Year:	2005
Journal:	Biochem J
Title:	The septin Sept5/CDCrel-1 competes with alpha-SNAP for binding to the SNARE complex.
Volume:	385
Issue:	Pt 2
Pages:	347-53

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Publication

11242049 | J:67409

First Author:	Lindsay EA
Year:	2001
Journal:	Nature
Title:	Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
Volume:	410
Issue:	6824
Pages:	97-101

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Publication

16684884 | J:110101

First Author:	Paylor R
Year:	2006
Journal:	Proc Natl Acad Sci U S A
Title:	Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.
Volume:	103
Issue:	20
Pages:	7729-34

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Publication

39638997 | J:359574

First Author:	Eom TY
Year:	2024
Journal:	Nat Commun
Title:	Tbx1 haploinsufficiency leads to local skull deformity, paraflocculus and flocculus dysplasia, and motor-learning deficit in 22q11.2 deletion syndrome.
Volume:	15
Issue:	1
Pages:	10510

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Publication

21821099 | J:184660

First Author:	Kvajo M
Year:	2012
Journal:	Neuroscience
Title:	Avoiding mouse traps in schizophrenia genetics: lessons and promises from current and emerging mouse models.
Volume:	211

Pages:	136-64

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Publication

15489334 | -

First Author:	Gerhard DS
Year:	2004
Journal:	Genome Res
Title:	The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Volume:	14
Issue:	10B
Pages:	2121-7

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