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siRNA therapeutics: big potential from small RNAs

Gene therapy, 2005-01, Vol.12 (1), p.5-11

2005

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Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Nature genetics, 2000-09, Vol.26 (1), p.81-84

2000

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Mutation in the Gene for Bone Morphogenetic Protein Receptor II as a Cause of Primary Pulmonary Hypertension in a Large Kindred

The New England journal of medicine, 2001-08, Vol.345 (5), p.319-324

2001

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Mutations in PROP1 cause familial combined pituitary hormone deficiency

Nature genetics, 1998-02, Vol.18 (2), p.147-149

1998

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Role of the Angiotensin Type 2 Receptor Gene in Congenital Anomalies of the Kidney and Urinary Tract, CAKUT, of Mice and Men

Molecular cell, 1999, Vol.3 (1), p.1-10

1999

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Gross BMPR2 gene rearrangements constitute a new cause for primary pulmonary hypertension

Genetics in medicine, 2005-03, Vol.7 (3), p.169-174

2005

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Multilocus Analysis of Hypertension: A Hierarchical Approach

Human heredity, 2004-01, Vol.57 (1), p.28-38

2004

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Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.917-923

1999

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Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32

Nature genetics, 1997-03, Vol.15 (3), p.277-280

1997

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The molecular genetics of growth hormone deficiency

Human genetics, 1998-09, Vol.103 (3), p.255-272

1998

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Characterization of an Intron Splice Enhancer that Regulates Alternative Splicing of Human GH Pre-mRNA

Human molecular genetics, 1998-09, Vol.7 (9), p.1491-1496

1998

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Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis

The New England journal of medicine, 2007-03, Vol.356 (13), p.1317-1326

2007

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Transcripts from a novel BMPR2 termination mutation escape nonsense mediated decay by downstream translation re-initiation: implications for treating pulmonary hypertension

Clinical genetics, 2010-03, Vol.77 (3), p.280-286

2010

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Nucleic acid aptamers for biosensors and bio-analytical applications

Analyst (London), 2009-09, Vol.134 (9), p.1765-1775

2009

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Molecular recognition of acute myeloid leukemia using aptamers

Leukemia, 2009-02, Vol.23 (2), p.235-244

2009

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Clinical and Pathologic Features of Familial Interstitial Pneumonia

American journal of respiratory and critical care medicine, 2005-11, Vol.172 (9), p.1146-1152

2005

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Isolated growth hormone deficiency type II caused by a point mutation that alters both splice site strength and splicing enhancer function

Clinical genetics, 2008-12, Vol.74 (6), p.539-545

2008

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Genetic basis of pulmonary arterial hypertension: Current understanding and future directions

Journal of the American College of Cardiology, 2004-06, Vol.43 (12), p.S33-S39

2004

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Interpreting FCI scores: Normalized gain, preinstruction scores, and scientific reasoning ability

American journal of physics, 2005-12, Vol.73 (12), p.1172-1182

2005

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CD4+ T cell activation and tolerance induction in B cell knockout mice

The Journal of experimental medicine, 1996-04, Vol.183 (4), p.1339-1344

1996

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Marine macroalgal biodiversity hotspots: why is there high species richness and endemism in southern Australian marine benthic flora?

Biodiversity and conservation, 2001-09, Vol.10 (9), p.1555-1577

Phillips, Julie A

2001

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Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening

American journal of human genetics, 1996-03, Vol.58 (3), p.617-627

1996

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Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF

Thorax, 2004-11, Vol.59 (11), p.977-980

2004

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Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls

European journal of endocrinology, 1997-11, Vol.137 (5), p.474-481

1997

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Premarital cohabitation and marital disruption among white, black, and Mexican American women

Journal of marriage and family, 2005-05, Vol.67 (2), p.296-314

2005

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siRNA therapeutics: big potential from small RNAs

Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Mutation in the Gene for Bone Morphogenetic Protein Receptor II as a Cause of Primary Pulmonary Hypertension in a Large Kindred

Mutations in PROP1 cause familial combined pituitary hormone deficiency

Role of the Angiotensin Type 2 Receptor Gene in Congenital Anomalies of the Kidney and Urinary Tract, CAKUT, of Mice and Men

Gross BMPR2 gene rearrangements constitute a new cause for primary pulmonary hypertension

Multilocus Analysis of Hypertension: A Hierarchical Approach

Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32

The molecular genetics of growth hormone deficiency

Characterization of an Intron Splice Enhancer that Regulates Alternative Splicing of Human GH Pre-mRNA

Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis

Transcripts from a novel BMPR2 termination mutation escape nonsense mediated decay by downstream translation re-initiation: implications for treating pulmonary hypertension

Nucleic acid aptamers for biosensors and bio-analytical applications

Molecular recognition of acute myeloid leukemia using aptamers

Clinical and Pathologic Features of Familial Interstitial Pneumonia

Isolated growth hormone deficiency type II caused by a point mutation that alters both splice site strength and splicing enhancer function

Genetic basis of pulmonary arterial hypertension: Current understanding and future directions

Interpreting FCI scores: Normalized gain, preinstruction scores, and scientific reasoning ability

CD4+ T cell activation and tolerance induction in B cell knockout mice

Marine macroalgal biodiversity hotspots: why is there high species richness and endemism in southern Australian marine benthic flora?

Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening

Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF

Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls

Premarital cohabitation and marital disruption among white, black, and Mexican American women

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