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The Requirement for Carotenoids in the Assembly and Function of the Photosynthetic Complexes in Chlamydomonas reinhardtii

Plant physiology (Bethesda), 2013-01, Vol.161 (1), p.535-546

2013

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Connexin-26 mutations in sporadic and inherited sensorineural deafness

The Lancet (British edition), 1998-02, Vol.351 (9100), p.394-398

1998

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Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

Human molecular genetics, 1997-09, Vol.6 (9), p.1605-1609

1997

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Infants Tolerate Spinal Anesthesia with Minimal Overall Autonomic Changes: Analysis of Heart Rate Variability in Former Premature Infants Undergoing Hernia Repair

Anesthesia and analgesia, 1995-01, Vol.80 (1), p.20-27

1995

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Analysis of Clinically Relevant Single-Nucleotide Polymorphisms by Use of Microelectronic Array Technology

Clinical chemistry (Baltimore, Md.), 2002-12, Vol.48 (12), p.2124-2130

2002

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Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform

Genome research, 2005-08, Vol.15 (8), p.1168-1176

2005

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Self-Protection by Cardiac Myocytes Against Hypoxia and Hyperoxia

Circulation research, 1999-10, Vol.85 (8), p.690-698

1999

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Differential expression of Fcγ RIIA, Fcγ RIIB and Fcγ RIIC in hematopoietic cells: Analysis of transcripts

Molecular immunology, 1993-04, Vol.30 (5), p.451-460

1993

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Rheologic Predictors of the Severity of the Painful Sickle Cell Crisis

Blood, 1988-10, Vol.72 (4), p.1216-1223

1988

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Parallel molecular genetic analysis

European journal of human genetics : EJHG, 1998-09, Vol.6 (5), p.417-429

1998

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Vascular endothelial cell-cardiac myocyte crosstalk in achieving a balance between energy supply and energy use

Advances in experimental medicine and biology, 1998, Vol.453, p.507

1998

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Variation in human FCGR2C gene copy number

Immunogenetics (New York), 1994-10, Vol.40 (6), p.456-456

1994

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The Xerocytosis of Hb SC Disease

Blood, 1987-01, Vol.69 (1), p.124-130

1987

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Characterization of the 5′-flanking transcriptional regulatory region of the human Fcγ receptor gene, Fcγ RIIA

Molecular immunology, 1992-10, Vol.29 (10), p.1165-1174

1992

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Fluorescence-based DNA minisequence analysis for detection of known single-base changes in genomic DNA

Molecular and cellular probes, 1995-06, Vol.9 (3), p.175-182

1995

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Polymerase chain reaction (PCR) for detection of PstI polymorphism in the human PF4 gene

Nucleic acids research, 1990-10, Vol.18 (19), p.5919-5919

1990

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Interaction of a rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of α thalassemia

Blood, 1994-06, Vol.83 (11), p.3356-3362

1994

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A large deletion encompassing the entire α-like globin gene cluster in a family of Northern European extraction

Nucleic acids research, 1988-12, Vol.16 (23), p.11223-11235

1988

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Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the ΔF508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) gene

Molecular and cellular probes, 1992-08, Vol.6 (4), p.353-356

1992

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Protection of uninfected human bone marrow cells in long-term culture from G418 toxicity after retroviral-mediated transfer of the NEOr gene

Experimental cell research, 1988-11, Vol.179 (1), p.168-180

1988

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Frequent occurrence of a ζ-globin-region deletion in american blacks accounts for a previously-described restriction site polymorphism

Biochemical and biophysical research communications, 1984-12, Vol.125 (2), p.817-823

1984

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The Effect of Alpha Thalassemia on the Clinical Course of Hemoglobin SC Disease

Annals of the New York Academy of Sciences, 1989-07, Vol.565 (1), p.365-366

1989

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Alpha-Gene Deletions in Black Newborn Infants With Hb Bart’s

Blood, 1980-11, Vol.56 (5), p.931-933

1980

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Duchenne/becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategies

American journal of medical genetics, 1993-12, Vol.48 (4), p.200-208

1993

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Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: Clinical observations and genetic analysis

American journal of medical genetics, 1995-11, Vol.59 (2), p.218-224

1995

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The Requirement for Carotenoids in the Assembly and Function of the Photosynthetic Complexes in Chlamydomonas reinhardtii

Connexin-26 mutations in sporadic and inherited sensorineural deafness

Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

Infants Tolerate Spinal Anesthesia with Minimal Overall Autonomic Changes: Analysis of Heart Rate Variability in Former Premature Infants Undergoing Hernia Repair

Analysis of Clinically Relevant Single-Nucleotide Polymorphisms by Use of Microelectronic Array Technology

Region-specific detection of neuroblastoma loss of heterozygosity at multiple loci simultaneously using a SNP-based tag-array platform

Self-Protection by Cardiac Myocytes Against Hypoxia and Hyperoxia

Differential expression of Fcγ RIIA, Fcγ RIIB and Fcγ RIIC in hematopoietic cells: Analysis of transcripts

Rheologic Predictors of the Severity of the Painful Sickle Cell Crisis

Parallel molecular genetic analysis

Vascular endothelial cell-cardiac myocyte crosstalk in achieving a balance between energy supply and energy use

Variation in human FCGR2C gene copy number

The Xerocytosis of Hb SC Disease

Characterization of the 5′-flanking transcriptional regulatory region of the human Fcγ receptor gene, Fcγ RIIA

Fluorescence-based DNA minisequence analysis for detection of known single-base changes in genomic DNA

Polymerase chain reaction (PCR) for detection of PstI polymorphism in the human PF4 gene

Interaction of a rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of α thalassemia

A large deletion encompassing the entire α-like globin gene cluster in a family of Northern European extraction

Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the ΔF508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) gene

Protection of uninfected human bone marrow cells in long-term culture from G418 toxicity after retroviral-mediated transfer of the NEOr gene

Frequent occurrence of a ζ-globin-region deletion in american blacks accounts for a previously-described restriction site polymorphism

The Effect of Alpha Thalassemia on the Clinical Course of Hemoglobin SC Disease

Alpha-Gene Deletions in Black Newborn Infants With Hb Bart’s

Duchenne/becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategies

Infundibulopelvic stenosis, multicystic kidney, and calyectasis in a kindred: Clinical observations and genetic analysis

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