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Polymorphisms in glucocorticoid receptor gene and the outcome of childhood acute lymphoblastic leukemia (ALL)

Leukemia research, 2010-04, Vol.34 (4), p.492-497

2010

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Phosphodiesterase Type 4D Gene Polymorphism: Association with the Response to Short-Acting Bronchodilators in Paediatric Asthma Patients

Mediators of Inflammation, 2011-01, Vol.2011 (2011), p.113-118

2011

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Variants of the KCNMB3 regulatory subunit of maxi BK channels affect channel inactivation

Physiological genomics, 2003-11, Vol.15 (3), p.191-198

2003

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Polymorphisms of asparaginase pathway and asparaginase-related complications in children with acute lymphoblastic leukemia

Clinical cancer research, 2015-01, Vol.21 (2), p.329-334

2015

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Polymorphisms in multidrug resistance-associated protein gene 4 is associated with outcome in childhood acute lymphoblastic leukemia

Blood, 2009-08, Vol.114 (7), p.1383-1386

2009

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ATF5 polymorphisms influence ATF function and response to treatment in children with childhood acute lymphoblastic leukemia

Blood, 2011-11, Vol.118 (22), p.5883-5890

2011

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RGS 5 gene and therapeutic response to short acting bronchodilators in paediatric asthma patients

Pediatric pulmonology, 2013-10, Vol.48 (10), p.970-975

2013

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RGS5 gene and therapeutic response to short acting bronchodilators in paediatric asthma patients

Pediatric pulmonology, 2013-10, Vol.48 (10), p.970-975

2013

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Bim Polymorphisms: Influence on Function and Response to Treatment in Children with Acute Lymphoblastic Leukemia

Clinical cancer research, 2013-09, Vol.19 (18), p.5240-5249

2013

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Role of NOS3 DNA variants in externalizing behavioral problems observed in childhood leukemia survivors

Journal of pediatric hematology/oncology, 2013-05, Vol.35 (4), p.e157-e162

2013

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Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

Annals of neurology, 1999-02, Vol.45 (2), p.200-206

1999

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Genetics of Vitamin D 1α-Hydroxylase Deficiency in 17 Families

American journal of human genetics, 1998-12, Vol.63 (6), p.1694-1702

1998

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Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17q

Epilepsy research, 2010-01, Vol.88 (1), p.65-75

2010

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Mapping of a Gene Determining Familial Partial Epilepsy with Variable Foci to Chromosome 22q11-q12

American journal of human genetics, 1999-12, Vol.65 (6), p.1698-1710

1999

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Linkage Mapping by Simultaneous Screening of Multiple Polymorphic Loci Using Alu Oligonucleotide-Directed PCR

Proceedings of the National Academy of Sciences - PNAS, 1992-09, Vol.89 (18), p.8448-8451

1992

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The Genetic Clock and the Age of the Founder Effect in Growing Populations: A Lesson from French Canadians and Ashkenazim

American journal of human genetics, 1997-09, Vol.61 (3), p.768-771

1997

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A missense mutation (W155R) in an American patient with Friedreich Ataxia

Human mutation, 1999, Vol.13 (6), p.506-506

1999

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Mapping autosomal recessive vitamin D dependency type I to chromosome 12q14 by linkage analysis

American journal of human genetics, 1990-07, Vol.47 (1), p.28-36

1990

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Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13–14

Journal of bone and mineral research, 1992-12, Vol.7 (12), p.1447-1453

1992

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Linkage disequilibrium analysis in young populations : Pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

American journal of human genetics, 1996-09, Vol.59 (3), p.633-643

1996

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Human 25‐hydroxyvitamin D 24‐hydroxylase cytochrome P450 subunit maps to a different chromosomal location than that of pseudovitamin D‐deficient rickets

Journal of bone and mineral research, 1993-11, Vol.8 (11), p.1397-1406

1993

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The in vitro DNA conformation of the Friedreich's ataxia repeat sequence mutation correlates with in vivo inhibition of gene expression and DNA replication [Abstract]

Clinical and investigative medicine, 1999-04, Vol.22 (2), p.67

1999

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Isobutyl acetate: electronic state spectroscopy by high-resolution vacuum ultraviolet photoabsorption, He(I) photoelectron spectroscopy and ab initio calculations

The European physical journal. D, Atomic, molecular, and optical physics, 2017-05, Vol.71 (5), p.1-8, Article 129

2017

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Electronic state spectroscopy by high-resolution vacuum ultraviolet photoabsorption, He(I) photoelectron spectroscopy and ab initio calculations of ethyl acetate

The European physical journal. D, Atomic, molecular, and optical physics, 2016-06, Vol.70 (6), p.1-9, Article 138

2016

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Polymorphisms in glucocorticoid receptor gene and the outcome of childhood acute lymphoblastic leukemia (ALL)

Phosphodiesterase Type 4D Gene Polymorphism: Association with the Response to Short-Acting Bronchodilators in Paediatric Asthma Patients

Variants of the KCNMB3 regulatory subunit of maxi BK channels affect channel inactivation

Polymorphisms of asparaginase pathway and asparaginase-related complications in children with acute lymphoblastic leukemia

Polymorphisms in multidrug resistance-associated protein gene 4 is associated with outcome in childhood acute lymphoblastic leukemia

ATF5 polymorphisms influence ATF function and response to treatment in children with childhood acute lymphoblastic leukemia

RGS 5 gene and therapeutic response to short acting bronchodilators in paediatric asthma patients

RGS5 gene and therapeutic response to short acting bronchodilators in paediatric asthma patients

Bim Polymorphisms: Influence on Function and Response to Treatment in Children with Acute Lymphoblastic Leukemia

Role of NOS3 DNA variants in externalizing behavioral problems observed in childhood leukemia survivors

Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

Genetics of Vitamin D 1α-Hydroxylase Deficiency in 17 Families

Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17q

Mapping of a Gene Determining Familial Partial Epilepsy with Variable Foci to Chromosome 22q11-q12

Linkage Mapping by Simultaneous Screening of Multiple Polymorphic Loci Using Alu Oligonucleotide-Directed PCR

The Genetic Clock and the Age of the Founder Effect in Growing Populations: A Lesson from French Canadians and Ashkenazim

A missense mutation (W155R) in an American patient with Friedreich Ataxia

Mapping autosomal recessive vitamin D dependency type I to chromosome 12q14 by linkage analysis

Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13–14

Linkage disequilibrium analysis in young populations : Pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

Human 25‐hydroxyvitamin D 24‐hydroxylase cytochrome P450 subunit maps to a different chromosomal location than that of pseudovitamin D‐deficient rickets

The in vitro DNA conformation of the Friedreich's ataxia repeat sequence mutation correlates with in vivo inhibition of gene expression and DNA replication [Abstract]

Diagnostic microRNA profiling in cutaneous T-cell lymphoma (CTCL)

Isobutyl acetate: electronic state spectroscopy by high-resolution vacuum ultraviolet photoabsorption, He(I) photoelectron spectroscopy and ab initio calculations

Electronic state spectroscopy by high-resolution vacuum ultraviolet photoabsorption, He(I) photoelectron spectroscopy and ab initio calculations of ethyl acetate

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