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Sankar Surendran

university of texas system

H指数:24

被引数:2,397

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Severity of pulmonary hypertension and pregnancy outcomes: newer insights from the M-PAC registry

EUROPEAN HEART JOURNAL

IF35.6

2024-10-280

PRE

Possible role of Fas antigen (CD 95) in human amniotic epithelial cell death:: An in vitro study

CELL BIOLOGY INTERNATIONAL

IF3.1

2013-01-027

PREAI

Arginine stimulates cdx2-transformed intestinal epithelial cell migration via a mechanism requiring both nitric oxide and phosphorylation of p70 S6 kinase

JOURNAL OF NUTRITION

IF3.8

2008-09-0185

OAAI

Canavan disease: A monogenic trait with complex genomic interaction (vol 80, pg 74, 2003)

MOLECULAR GENETICS AND METABOLISM

IF3.5

2006-03-010

PREAI

Aspartoacylase gene knockout in the mouse: Impact on reproduction

REPRODUCTIVE TOXICOLOGY

IF2.8

2005-07-016

PRE

Abnormal expression of genes associated with development and inflammation in the heart of mouse maternal Phenylketonuria offspring

INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY

IF2.6

2005-07-0115

PREAI

Expression of calpastatin, minopontin, NIPSNAP1, rabaptin-5 and neuronatin in the phenylketonuria (PKU) mouse brain: Possible role on cognitive defect seen in PKU

NEUROCHEMISTRY INTERNATIONAL

IF4

2005-06-0125

PREAI

Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2005-03-22164

OAAI

Aspartoacylase gene knockout results in severe vacuolation in the white matter and gray matter of the spinal cord in the mouse

NEUROBIOLOGY OF DISEASE

IF5.6

2005-03-0121

PREAI

Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2004-11-19168

OAAI

Trends in enzyme therapy for phenylketonuria

MOLECULAR THERAPY

IF12

2004-08-0187

OAAI

Biopterin responsive phenylalanine hydroxylase deficiency

GENETICS IN MEDICINE

IF6.2

2004-01-0154

OAAI

Canavan disease: a monogenic trait with complex genomic interaction

MOLECULAR GENETICS AND METABOLISM

IF3.5

2003-09-0137

PREAI

Expression of glutamate transporter, GABRA6, serine proteinase inhibitor 2 and low levels of glutamate and GABA in the brain of knock-out mouse for Canavan disease

BRAIN RESEARCH BULLETIN

IF3.7

2003-08-0120

PREAI

Adeno-associated virus-mediated aspartoacylase gene transfer to the brain of knockout mouse for Canavan disease

腺相关病毒介导的天冬氨酸酰化酶基因转移至Canavan病基因敲除小鼠的大脑

MOLECULAR THERAPY

IF12

2003-05-0191

OAAI

High levels of orexin A in the brain of the mouse model for phenylketonuria: Possible role of orexin A in hyperactivity seen in children with PKU

NEUROCHEMICAL RESEARCH

IF3.8

2003-01-0110

PREAI