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WNT9B gene

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

Papers overview

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2016
2016
Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) is a well-known malformation pattern of the Müllerian ducts (MDs) characterized… Expand
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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… Expand
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2014
2014
BACKGROUND The heritable multifactorial etiology of human nonsyndromic cleft lip with or without cleft palate (CL ± P) is not… Expand
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2014
2014
Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a rare congenital female genital anomaly, which is caused by aplasia of the… Expand
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Highly Cited
2011
Highly Cited
2011
The primary excretory organ in vertebrates is the kidney, which is responsible for blood filtration, solute homeostasis and pH… Expand
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Highly Cited
2010
Highly Cited
2010
β-catenin-dependent Wnt signaling is initiated as Wnt binds to both the receptor FZD and coreceptor LRP5/6, which then assembles… Expand
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Highly Cited
2010
Highly Cited
2010
Wnt/β-catenin signaling is initiated at the cell surface by association of secreted Wnt with its receptors Frizzled (Fz) and low… Expand
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Highly Cited
2009
Highly Cited
2009
Although many vertebrate organs, such as kidneys, lungs and liver, are composed of epithelial tubules, little is known of the… Expand
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Highly Cited
2007
Highly Cited
2007
Mammalian nephrons form as a result of a complex morphogenesis and patterning of a simple epithelial precursor, the renal vesicle… Expand
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2001
2001
WNT14B was cloned and characterized in this study. WNT14B encoded 357-amino acid WNT family protein with the signal peptide and… Expand
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