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Etiology of a genetically complex seizure disorder in Celf4 mutant mice

Genes, brain and behavior, 2011-10, Vol.10 (7), p.765-777

2011

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Effects of estrogen on cognition, mood, and cerebral blood flow in AD: a controlled study

Neurology, 2000-06, Vol.54 (11), p.2061-2066

2000

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Platelet‐activating factor‐acetylhydrolase A379V (exon 11) gene polymorphism is an independent and functional risk factor for premature myocardial infarction

Journal of thrombosis and haemostasis, 2006-05, Vol.4 (5), p.1023-1028

2006

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Mitochondrial deoxyribonucleic acid 4977-bp deletion is associated with diminished fertility and motility of human sperm

Biology of reproduction, 1995-04, Vol.52 (4), p.729-736

1995

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High prevalence of incidental brain findings in primary dysmenorrhoea

European journal of pain, 2015-09, Vol.19 (8), p.1071-1074

2015

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Risk Factors Contributing to Early Occurrence of Port Site Metastases of Laparoscopic Surgery for Malignancy

Gynecologic oncology, 1999-01, Vol.72 (1), p.38-44

1999

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Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa

Molecular human reproduction, 1998-07, Vol.4 (7), p.657-666

1998

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A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib

Cancer cell, 2005-11, Vol.8 (5), p.407-419

2005

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Port Site Metastasis after Laparoscopic-Assisted Vaginal Hysterectomy for Endometrial Cancer: Possible Mechanisms and Prevention

Gynecologic oncology, 1997-07, Vol.66 (1), p.151-155

1997

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Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia

Journal of medical genetics, 1996-05, Vol.33 (5), p.371-375

1996

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Structure−Activity Relationship Studies of Salinosporamide A (NPI-0052), a Novel Marine Derived Proteasome Inhibitor

Journal of medicinal chemistry, 2005-06, Vol.48 (11), p.3684-3687

2005

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Stromelysin‐1 promoter 5A/6A polymorphism is an independent genetic prognostic risk factor and interacts with smoking cessation after index premature myocardial infarction

Journal of thrombosis and haemostasis, 2005-09, Vol.3 (9), p.1998-2005

2005

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Role of BMK1 in regulation of growth factor-induced cellular responses

Immunologic research, 2000-01, Vol.21 (2-3), p.233-237

2000

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A Combined Cross-sectional and Longitudinal Study of Predicting Metabolic Syndrome and Cardiovascular Disease by Using Haemoglobin in the Elderly

West Indian medical journal, 2017-01

2017

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Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese

Human genetics, 1998-09, Vol.103 (3), p.304-310

1998

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MEKK3 Directly Regulates MEK5 Activity as Part of the Big Mitogen-activated Protein Kinase 1 (BMK1) Signaling Pathway

The Journal of biological chemistry, 1999-12, Vol.274 (51), p.36035-36038

1999

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Association Between FRAX Without BMD and Incidence of Falls in Middle-Aged and Old People: An Epidemiological Cohort Survey

Journal of clinical densitometry, 2014-07, Vol.17 (3), p.416-417

2014

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G-33a mutation in the promoter region of thrombomodulin gene and its association with coronary artery disease and plasma soluble thrombomodulin levels

The American journal of cardiology, 2000, Vol.85 (1), p.8-12

2000

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Gonadotropin-releasing hormone-agonist as a neoadjuvant therapy for Sertoli–Leydig cell tumors of the ovary

International journal of gynecology and obstetrics, 1999-08, Vol.66 (2), p.189-190

1999

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An Autologous Oral DNA Vaccine Protects against Murine Melanoma

Proceedings of the National Academy of Sciences - PNAS, 2000-05, Vol.97 (10), p.5492-5497

2000

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Steroid cell tumors of the ovary: clinical, ultrasonic, and MRI diagnosis—a case report

European journal of radiology, 1998-02, Vol.26 (3), p.269-273

1998

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BMK1 Mediates Growth Factor-induced Cell Proliferation through Direct Cellular Activation of Serum and Glucocorticoid-inducible Kinase

The Journal of biological chemistry, 2001-03, Vol.276 (12), p.8631-8634

2001

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Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese

The journal of clinical endocrinology and metabolism, 2000-02, Vol.85 (2), p.597-600

2000

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Use of a long-acting gonadotropin-releasing hormone agonist for treatment of steroid cell tumors of the ovary

Fertility and sterility, 1998-02, Vol.69 (2), p.353-355

1998

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Posterior uterine wall rupture during labour

Human reproduction (Oxford), 2000-05, Vol.15 (5), p.1198-1199

2000

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Etiology of a genetically complex seizure disorder in Celf4 mutant mice

Effects of estrogen on cognition, mood, and cerebral blood flow in AD: a controlled study

Platelet‐activating factor‐acetylhydrolase A379V (exon 11) gene polymorphism is an independent and functional risk factor for premature myocardial infarction

Mitochondrial deoxyribonucleic acid 4977-bp deletion is associated with diminished fertility and motility of human sperm

High prevalence of incidental brain findings in primary dysmenorrhoea

Risk Factors Contributing to Early Occurrence of Port Site Metastases of Laparoscopic Surgery for Malignancy

Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa

A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib

Port Site Metastasis after Laparoscopic-Assisted Vaginal Hysterectomy for Endometrial Cancer: Possible Mechanisms and Prevention

Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia

Structure−Activity Relationship Studies of Salinosporamide A (NPI-0052), a Novel Marine Derived Proteasome Inhibitor

Stromelysin‐1 promoter 5A/6A polymorphism is an independent genetic prognostic risk factor and interacts with smoking cessation after index premature myocardial infarction

Role of BMK1 in regulation of growth factor-induced cellular responses

A Combined Cross-sectional and Longitudinal Study of Predicting Metabolic Syndrome and Cardiovascular Disease by Using Haemoglobin in the Elderly

Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese

MEKK3 Directly Regulates MEK5 Activity as Part of the Big Mitogen-activated Protein Kinase 1 (BMK1) Signaling Pathway

Association Between FRAX Without BMD and Incidence of Falls in Middle-Aged and Old People: An Epidemiological Cohort Survey

G-33a mutation in the promoter region of thrombomodulin gene and its association with coronary artery disease and plasma soluble thrombomodulin levels

Gonadotropin-releasing hormone-agonist as a neoadjuvant therapy for Sertoli–Leydig cell tumors of the ovary

An Autologous Oral DNA Vaccine Protects against Murine Melanoma

Steroid cell tumors of the ovary: clinical, ultrasonic, and MRI diagnosis—a case report

BMK1 Mediates Growth Factor-induced Cell Proliferation through Direct Cellular Activation of Serum and Glucocorticoid-inducible Kinase

Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese

Use of a long-acting gonadotropin-releasing hormone agonist for treatment of steroid cell tumors of the ovary

Posterior uterine wall rupture during labour

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