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SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

Genetics in medicine, 2008-08, Vol.10 (8), p.586-592

2008

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Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy

Haematologica (Roma), 2011-01, Vol.96 (1), p.24-32

2011

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Pulmonary hypertension and nitric oxide depletion in sickle cell disease

Blood, 2010-08, Vol.116 (5), p.687-692

2010

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Quantitative trait loci for baseline white blood cell count, platelet count, and mean platelet volume

Mammalian genome, 2005-10, Vol.16 (10), p.749-763

2005

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Quantitative trait loci for baseline erythroid traits

Mammalian genome, 2006-04, Vol.17 (4), p.298-309

2006

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Prevention and management of stroke in sickle cell anemia

Hematology, 2006, Vol.2006 (1), p.54-57

Platt, Orah S

2006

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Quantitative trait loci for peripheral blood cell counts: a study in baboons

Mammalian genome, 2007-05, Vol.18 (5), p.361-372

2007

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Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss

Physiological genomics, 2009-08, Vol.38 (3), p.281-290

2009

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Protective effects of phosphodiesterase‐4 (PDE‐4) inhibition in the early phase of pulmonary arterial hypertension in transgenic sickle cell mice

The FASEB journal, 2008-06, Vol.22 (6), p.1849-1860

2008

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Age- and gender-dependent obesity in individuals with 16p11.2 deletion

Journal of genetics and genomics, 2011-09, Vol.38 (9), p.403-409

2011

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Genetic influences on peripheral blood cell counts: a study in baboons

Blood, 2005-08, Vol.106 (4), p.1210-1214

2005

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Transposing Sequences between Fetal and Adult Hemoglobins Indicates Which Subunits and Regulatory Molecule Interfaces Are Functionally Related

Biochemistry (Easton), 2000-04, Vol.39 (13), p.3774-3781

2000

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Association Between Microdeletion and Microduplication at 16p11.2 and Autism

Obstetrical & gynecological survey, 2008-06, Vol.63 (6), p.361-363

2008

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Sickle cell anemia as an inflammatory disease

The Journal of clinical investigation, 2000-08, Vol.106 (3), p.337-338

Platt, O S

2000

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Sickle cell paths converge on hydroxyurea

Nature medicine, 1995-04, Vol.1 (4), p.307-308

Platt, Orah S

1995

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Safety of Hydroxyurea in Children With Sickle Cell Anemia: Results of the HUG-KIDS Study, a Phase I/II Trial

Blood, 1999-09, Vol.94 (5), p.1550-1554

1999

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Sickle Reticulocytes Adhere to VCAM-1

Blood, 1995-01, Vol.85 (1), p.268-274

1995

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Phosphodiesterase-4 Inhibition Reduces Ischemic/Reperfusion Liver Injury in a Mouse Model for Sickle Cell Disease

Blood, 2008-11, Vol.112 (11), p.1444-1444

2008

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Acquisition of mutans streptococci and caries prevalence in pediatric sickle cell anemia patients receiving long-term antibiotic therapy

Pediatric dentistry, 2005-05, Vol.27 (3), p.186

2005

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Editorial: The acute chest syndrome of sickle cell disease

The New England journal of medicine, 2000-06, Vol.342 (25), p.1904

Platt, Orah S

2000

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Therapy with oral clotrimazole induces inhibition of the Gardos channel and reduction of erythrocyte dehydration in patients with sickle cell disease

The Journal of clinical investigation, 1996-03, Vol.97 (5), p.1227-1234

1996

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Joint Estimation of Incidence and Diagnostic Error Rates from Irregular Longitudinal Data

Journal of the American Statistical Association, 1989-12, Vol.84 (408), p.972-979

1989

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Hydroxyurea: Effects on Hemoglobin F Production in Patients With Sickle Cell Anemia

Blood, 1992-05, Vol.79 (10), p.2555-2565

1992

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Reliability of Tanner stage assessments in a multi-center study

American journal of human biology, 1990, Vol.2 (5), p.503-510

1990

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A Large-Scale Mutagenesis and Strain Characterization Project To Identify Genetic Variability in Mice: Resources Available from the Jackson Laboratory Program for Genomic Applications (JAX PGA)

Blood, 2004-11, Vol.104 (11), p.1578-1578

2004

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SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

Abnormal modulation of cell protective systems in response to ischemic/reperfusion injury is important in the development of mouse sickle cell hepatopathy

Pulmonary hypertension and nitric oxide depletion in sickle cell disease

Quantitative trait loci for baseline white blood cell count, platelet count, and mean platelet volume

Quantitative trait loci for baseline erythroid traits

Prevention and management of stroke in sickle cell anemia

Quantitative trait loci for peripheral blood cell counts: a study in baboons

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss

Protective effects of phosphodiesterase‐4 (PDE‐4) inhibition in the early phase of pulmonary arterial hypertension in transgenic sickle cell mice

Age- and gender-dependent obesity in individuals with 16p11.2 deletion

Genetic influences on peripheral blood cell counts: a study in baboons

Transposing Sequences between Fetal and Adult Hemoglobins Indicates Which Subunits and Regulatory Molecule Interfaces Are Functionally Related

Association Between Microdeletion and Microduplication at 16p11.2 and Autism

Sickle cell anemia as an inflammatory disease

Sickle cell paths converge on hydroxyurea

Safety of Hydroxyurea in Children With Sickle Cell Anemia: Results of the HUG-KIDS Study, a Phase I/II Trial

Sickle Reticulocytes Adhere to VCAM-1

Phosphodiesterase-4 Inhibition Reduces Ischemic/Reperfusion Liver Injury in a Mouse Model for Sickle Cell Disease

Acquisition of mutans streptococci and caries prevalence in pediatric sickle cell anemia patients receiving long-term antibiotic therapy

Editorial: The acute chest syndrome of sickle cell disease

Therapy with oral clotrimazole induces inhibition of the Gardos channel and reduction of erythrocyte dehydration in patients with sickle cell disease

Joint Estimation of Incidence and Diagnostic Error Rates from Irregular Longitudinal Data

Hydroxyurea: Effects on Hemoglobin F Production in Patients With Sickle Cell Anemia

Reliability of Tanner stage assessments in a multi-center study

A Large-Scale Mutagenesis and Strain Characterization Project To Identify Genetic Variability in Mice: Resources Available from the Jackson Laboratory Program for Genomic Applications (JAX PGA)

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