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Red blood cell generation from human induced pluripotent stem cells: perspectives for transfusion medicine

Haematologica (Roma), 2010-10, Vol.95 (10), p.1651-1659

2010

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Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

Journal of medical genetics, 2001-06, Vol.38 (6), p.396-400

2001

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Distributed Weighted Matching

Distributed Computing, 2004, p.335-348

2004

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Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains

Human genetics, 2001-03, Vol.108 (2), p.140-147

2001

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The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro

Human molecular genetics, 2002-11, Vol.11 (23), p.2829-2836

2002

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Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro

Human mutation, 2005-06, Vol.25 (6), p.543-549

2005

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Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

Human mutation, 2002-02, Vol.19 (2), p.183-183

2002

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Efficient Adaptive Collect Using Randomization

Distributed Computing, 2004, p.159-173

2004

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An Induced Pluripotent Stem Cell Model for Friedreich's Ataxia (IN8-1.007)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.IN8-1.007-IN8-1.007

2012

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An Induced Pluripotent Stem Cell Model for Friedreich's Ataxia (P05.022)

Neurology, 2012-04, Vol.78 (Meeting Abstracts 1), p.P05-P05.022

2012

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A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein

Human genetics, 2005-10, Vol.117 (6), p.528-535

2005

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Ultrasound‐Guided Approaches to Improve Orthotopic Mouse Xenograft Models for Hepatocellular Carcinoma

Current protocols in mouse biology, 2019-06, Vol.9 (2), p.e62-n/a

2019

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Geometric Routing Without Geometry

Lecture notes in computer science, 2005, p.307-322

2005

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Efficient adaptive collect using randomization

Distributed computing, 2006-02, Vol.18 (3), p.179-188

2006

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Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients

Journal of molecular medicine (Berlin, Germany), 2002-02, Vol.80 (2), p.124-131

2002

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Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

Human mutation, 2001-08, Vol.18 (2), p.101-108

2001

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Cloning and Characterization of a Putative Human Glycerol 3-Phosphate Permease Gene (SLC37A1 or G3PP) on 21q22.3: Mutation Analysis in Two Candidate Phenotypes, DFNB10 and a Glycerol Kinase Deficiency

Genomics (San Diego, Calif.), 2000-12, Vol.70 (2), p.190-200

2000

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Catching a Viral Video

2010 IEEE International Conference on Data Mining Workshops, 2010, p.296-304

2010

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Refined Localization of Autosomal Recessive Nonsyndromic Deafness DFNB10 Locus Using 34 Novel Microsatellite Markers, Genomic Structure, and Exclusion of Six Known Genes in the Region

Genomics (San Diego, Calif.), 2000-08, Vol.68 (1), p.22-29

2000

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A cone-based distributed topology-control algorithm for wireless multi-hop networks

IEEE/ACM transactions on networking, 2005-02, Vol.13 (1), p.147-159

2005

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Bitcoin Transaction Malleability and MtGox

Computer Security - ESORICS 2014, p.313-326

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High-throughput discovery of novel developmental phenotypes

Nature (London), 2016-09, Vol.537 (7621), p.508-514

2016

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Algorithms for Wireless Capacity

IEEE/ACM transactions on networking, 2014-06, Vol.22 (3), p.745-755

2014

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Network correlated data gathering with explicit communication: NP-completeness and algorithms

IEEE/ACM transactions on networking, 2006-02, Vol.14 (1), p.41-54

2006

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Red blood cell generation from human induced pluripotent stem cells: perspectives for transfusion medicine

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

Distributed Weighted Matching

Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains

The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro

Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro

Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

Efficient Adaptive Collect Using Randomization

An Induced Pluripotent Stem Cell Model for Friedreich's Ataxia (IN8-1.007)

An Induced Pluripotent Stem Cell Model for Friedreich's Ataxia (P05.022)

A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein

Ultrasound‐Guided Approaches to Improve Orthotopic Mouse Xenograft Models for Hepatocellular Carcinoma

Geometric Routing Without Geometry

Efficient adaptive collect using randomization

Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients

Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

Cloning and Characterization of a Putative Human Glycerol 3-Phosphate Permease Gene (SLC37A1 or G3PP) on 21q22.3: Mutation Analysis in Two Candidate Phenotypes, DFNB10 and a Glycerol Kinase Deficiency

Catching a Viral Video

Refined Localization of Autosomal Recessive Nonsyndromic Deafness DFNB10 Locus Using 34 Novel Microsatellite Markers, Genomic Structure, and Exclusion of Six Known Genes in the Region

A cone-based distributed topology-control algorithm for wireless multi-hop networks

Bitcoin Transaction Malleability and MtGox

High-throughput discovery of novel developmental phenotypes

Algorithms for Wireless Capacity

Network correlated data gathering with explicit communication: NP-completeness and algorithms

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