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Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymes

Clinical chemistry (Baltimore, Md.), 1997-09, Vol.43 (9), p.1657-1659

1997

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Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus

Blood, 2003-06, Vol.101 (12), p.4808-4815

2003

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A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Blood, 1998-08, Vol.92 (4), p.1119-1124

1998

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A 13‐bp deletion in αIIb gene is a founder mutation that predominates in Palestinian‐Arab patients with Glanzmann thrombasthenia

Journal of thrombosis and haemostasis, 2005-12, Vol.3 (12), p.2764-2772

2005

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A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia

Journal of thrombosis and haemostasis, 2005-12, Vol.3 (12), p.2764

2005

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Evaluating the Short-Run Benefits of Six Department of Energy R&D Projects

The Journal of technology transfer, 2005-07, Vol.30 (3), p.287-301

2005

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Factor VIII gene rearrangement in hemophilia A carrier detection: a word of caution [letter]

Blood, 1994-08, Vol.84 (4), p.1351-1352

1994

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More on the Agenda

Social science quarterly, 1996-09, Vol.77 (3), p.516-519

1996

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Erratum: Aragonite crystalline matrix as an instructive microenvironment for neural development. Journal of Tissue Engineering and Regenerative Medicine 2008; 2: 463-471

Journal of tissue engineering and regenerative medicine, 2009-02, Vol.3 (2), p.160-160

2009

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XDH gene mutation is the underlying cause of classical xanthinuria: A second report

Kidney international, 2000-06, Vol.57 (6), p.2215-2220

2000

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SYNOVIAL AND SERUM LEVELS OF METHOTREXATE DURING METHOTREXATE THERAPY OF RHEUMATOID ARTHRITIS

Rheumatology (Oxford, England), 1989-10, Vol.28 (5), p.422-423

1989

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Detection of the Glanzmann's thrombasthenia mutations in Arab and Iraqi-Jewish patients by polymerase chain reaction and restriction analysis of blood or urine samples

Thrombosis and haemostasis, 1991, Vol.66 (4), p.500-504

1991

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One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews [see comments]

Blood, 1995-01, Vol.85 (2), p.429-432

1995

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Policy Gridlock in Waste Management: Balancing Federal and State Concerns

Policy studies journal, 1994, Vol.22 (4), p.589-603

1994

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The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin

Blood, 1997-10, Vol.90 (7), p.2654-2659

1997

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Benefit-cost analysis of Automotive Lightweighting Material projects

International journal of energy technology and policy, 2004, Vol.2 (4), p.369

2004

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Equity under and State Responses to the Superfund Amendments and Reauthorization Act of 1986

Policy sciences, 1992-05, Vol.25 (2), p.191-209

Peretz, Jean H.

1992

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Waste management agenda setting: a case of incorrect problem definition?

Waste management & research, 1998-06, Vol.16 (3), p.202-209

Peretz, Jean H.

1998

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Role of CYP2D6 polymorphism in predicting liver fibrosis progression rate in Caucasian patients with chronic hepatitis C

Liver international, 2006-04, Vol.26 (3), p.279-284

2006

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Age Estimates of Two Common Mutations Causing Factor XI Deficiency: Recent Genetic Drift Is Not Necessary for Elevated Disease Incidence among Ashkenazi Jews

American journal of human genetics, 1999-04, Vol.64 (4), p.1071-1075

1999

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Using Scenarios to Assess the Impact of Air Pollution in the Great Smoky Mountains National Park

Public works management & policy, 2005-10, Vol.10 (2), p.170-185

2005

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Screening for Down syndrome in the second trimester of pregnancy

European journal of obstetrics & gynecology and reproductive biology, 1994-05, Vol.55 (1), p.15-16

1994

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Molecular biology techniques in the diagnosis of monogenic diseases

Clinica chimica acta, 1994-02, Vol.225 (1), p.S35-S50

1994

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Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombasthenia

Blood, 2001-08, Vol.98 (4), p.1063-1069

2001

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Method for Gauging Limits to Foresight in Environmental Decision Making

Technological forecasting & social change, 2001-05, Vol.67 (1), p.35-53

2001

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Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymes

Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

A 13‐bp deletion in αIIb gene is a founder mutation that predominates in Palestinian‐Arab patients with Glanzmann thrombasthenia

A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia

Evaluating the Short-Run Benefits of Six Department of Energy R&D Projects

Factor VIII gene rearrangement in hemophilia A carrier detection: a word of caution [letter]

More on the Agenda

Erratum: Aragonite crystalline matrix as an instructive microenvironment for neural development. Journal of Tissue Engineering and Regenerative Medicine 2008; 2: 463-471

XDH gene mutation is the underlying cause of classical xanthinuria: A second report

SYNOVIAL AND SERUM LEVELS OF METHOTREXATE DURING METHOTREXATE THERAPY OF RHEUMATOID ARTHRITIS

Detection of the Glanzmann's thrombasthenia mutations in Arab and Iraqi-Jewish patients by polymerase chain reaction and restriction analysis of blood or urine samples

One of the two common mutations causing factor XI deficiency in Ashkenazi Jews (type II) is also prevalent in Iraqi Jews, who represent the ancient gene pool of Jews [see comments]

Policy Gridlock in Waste Management: Balancing Federal and State Concerns

The Two Common Mutations Causing Factor XI Deficiency in Jews Stem From Distinct Founders: One of Ancient Middle Eastern Origin and Another of More Recent European Origin

Benefit-cost analysis of Automotive Lightweighting Material projects

Equity under and State Responses to the Superfund Amendments and Reauthorization Act of 1986

Waste management agenda setting: a case of incorrect problem definition?

Role of CYP2D6 polymorphism in predicting liver fibrosis progression rate in Caucasian patients with chronic hepatitis C

Age Estimates of Two Common Mutations Causing Factor XI Deficiency: Recent Genetic Drift Is Not Necessary for Elevated Disease Incidence among Ashkenazi Jews

Using Scenarios to Assess the Impact of Air Pollution in the Great Smoky Mountains National Park

Screening for Down syndrome in the second trimester of pregnancy

Molecular biology techniques in the diagnosis of monogenic diseases

Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombasthenia

Method for Gauging Limits to Foresight in Environmental Decision Making

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