WNT9B gene

Known as: WNT15, WNT9B, WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 9B 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1997-2017
02419972017

Papers overview

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2015
2015
BACKGROUND Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare syndrome that is characterized by congenital aplasia of the… (More)
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2015
2015
OBJECTIVE Nonsyndromic cleft lip with or without cleft palate (NSCL±P) is a common craniofacial anomaly of complex etiology in… (More)
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2014
2014
The WNT9B gene is a common organizing signal regulating different segments of the mammalian urogenital system and plays a primary… (More)
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2012
2012
Outgrowth and fusion of the lateral and medial nasal processes and of the maxillary process of the first branchial arch are… (More)
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2012
2012
The wingless-type MMTV integration site family (Wnt) signalling pathway plays a crucial role in craniofacial development… (More)
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2005
2005
WNT signals, transduced through Frizzled (FZD) receptors with extracellular WNT-binding domain and cytoplasmic Dishevelled… (More)
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2002
2002
WNT signals are transduced through seven-transmembrane-type WNT receptors encoded by Frizzled (FZD) genes to the beta-catenin… (More)
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2001
2001
WNT proteins play key roles in carcinogenesis. We have previously cloned and characterized WNT14 and WNT14B/WNT15. WNT14 and… (More)
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2001
2001
Human WNT3A and WNT14 cDNAs were cloned and characterized. WNT3A and WNT14 encoded WNT family protein of 352 and 365 amino acids… (More)
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1997
1997
The Wnt gene family consists of at least 15 structurally related genes that encode secreted extracellular signaling factors. Wnt… (More)
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