BRANCHIOOTIC SYNDROME 3 (disorder)

Known as: BO Syndrome 3, BOS3, BRANCHIOOTIC SYNDROME 3 
 
National Institutes of Health

Related topics

Related topics

8 relations
Accessory tragusAutosomal dominant inheritanceBranchiomaPreauricular Fistulae, Congenital
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Broader (1)

Branchio-Oto-Renal Syndrome

Papers overview

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2017
2017
Mesenchymal Stromal Cell Therapy for Chronic Lung Allograft Dysfunction: Results of a First‐in‐Man Study
Chronic lung transplant rejection (termed chronic lung allograft dysfunction [CLAD]) is the main impediment to long-term survival… (More)
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2015
2015
Giant nonlinearity via breaking parity-time symmetry: a route to low-threshold phonon diodes
  • Jing Zhang, Bo Peng, +6 authors Franco Nori
  • 2015
Jing Zhang,1,2,3,* Bo Peng,3 Şahin Kaya Özdemir,3,† Yu-xi Liu,2,4,‡ Hui Jing,5,6 Xin-you Lü,6,7 Yu-long Liu,4 Lan Yang,3,§ and… (More)
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2014
2014
De novo donor HLA-specific antibodies predict development of bronchiolitis obliterans syndrome after lung transplantation.
BACKGROUND Bronchiolitis obliterans syndrome (BOS) is the major cause of late graft failure after lung transplantation. The… (More)
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2014
2014
Lapatinib-incorporated lipoprotein-like nanoparticles: preparation and a proposed breast cancer-targeting mechanism
Aim:Lapatinib is a dual inhibitor of EGFR and human epidermal growth factor receptor 2 (HER2), and used to treat advanced breast… (More)
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2010
2010
Styryl Dyes as Two-Photon Excited Fluorescent Probes for DNA Detection and Two-Photon Laser Scanning Fluorescence Microscopy of Living Cells
Spectral-fluorescent properties of benzothiazole styryl monomer (Bos-3) and homodimer (DBos-21) dyes in presence of DNA were… (More)
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2008
2008
Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement.
We report on a 26-month-old boy with developmental delay and multiple congenital anomalies, including many features suggestive of… (More)
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2005
2005
Estimating a Semi-Parametric Duration Model without Specifying Heterogeneity
This paper presents a new estimator for the mixed proportional hazard model that allows for a nonparametric baseline hazard and… (More)
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Highly Cited
2004
Highly Cited
2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
Urinary tract malformations constitute the most frequent cause of chronic renal failure in the first two decades of life… (More)
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2003
2003
Diversité et valorisation au niveau local des ressources végétales forestières alimentaires du Bénin
Les formations végéta les existantes au Bénin constituent une source et un réservoir pote ntie l de pro luits alimenta ires. Très… (More)
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1996
1996
Defining genes that govern longevity in Caenorhabditis elegans.
We previously identified five regions on the chromosomal map of Caenorhabditis elegans, containing genes that help specify life… (More)
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