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Differential Myosin 5a splice variants in innervation of pelvic organs

Frontiers in physiology, 2023-12, Vol.14, p.1304537-1304537

2023

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Myosin 5a in the Urinary Bladder: Localization, Splice Variant Expression, and Functional Role in Neurotransmission

Frontiers in physiology, 2022-07, Vol.13, p.890102-890102

2022

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Myosin Va plays a role in nitrergic smooth muscle relaxation in gastric fundus and corpora cavernosa of penis

PloS one, 2014-02, Vol.9 (2), p.e86778-e86778

2014

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Upregulation of the coagulation factor VII gene during glucose deprivation is mediated by activating transcription factor 4

PloS one, 2012-07, Vol.7 (7), p.e40994

2012

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Expression of Myosin 5a splice variants in murine stomach

Neurogastroenterology and motility, 2021-10, Vol.33 (10), p.e14162-n/a

2021

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MP42-10 AUGMENTED BLADDER SMOOTH MUSCLE RESPONSIVENESS TO HYPERGLYCEMIA THROUGH A CAVEOLAE-DEPENDENT ACTIVATION OF RHO KINASE PATHWAY

The Journal of urology, 2017-04, Vol.197 (4), p.e548-e548

2017

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MP42-14 PURINERGIC P2X4 RECEPTOR EXPRESSION AND FUNCTION IN RODENT BLADDER SMOOTH MUSCLE

The Journal of urology, 2017-04, Vol.197 (4), p.e549-e549

2017

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Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity

Thrombosis and haemostasis, 2002-11, Vol.88 (5), p.750

2002

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Polymorphisms in the factor VII gene and ischemic stroke in young adults

Blood coagulation & fibrinolysis, 2010-07, Vol.21 (5), p.442-447

2010

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CCAAT/Enhancer-binding Protein-β Participates in Insulin-responsive Expression of the Factor VII Gene

The Journal of biological chemistry, 2007-10, Vol.282 (43), p.31156-31165

2007

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A new mutation in the HNF4 binding region of the factor VII promoter in a patient with severe factor VII deficiency

Blood, 2000-12, Vol.96 (13), p.4370-4372

2000

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Severe Factor VII Deficiency Due to a Mutation Disrupting an Sp1 Binding Site in the Factor VII Promoter

Blood, 1998-09, Vol.92 (5), p.1639-1645

1998

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Suppression of dimethylhydrazine-induced carcinogenesis in mice by dietary addition of the Bowman-Birk protease inhibitor

Cancer research (Chicago, Ill.), 1990-02, Vol.50 (3), p.580-586

1990

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AB295. SPR-22 Functional relevance of purinergic P2X4R in bladder smooth muscle

Translational andrology and urology, 2016-12, Vol.5 (S2), p.AB295-AB295

2016

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Mechanism underlying factor VII deficiency in Jewish populations with the Ala244Val mutation

British journal of haematology, 1999-06, Vol.105 (4), p.1101-1108

1999

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CCAAT/Enhancer-binding Protein-Î² Participates in Insulin-responsive Expression of the Factor VII Gene

The Journal of biological chemistry, 2007-10, Vol.282 (43), p.31156

2007

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Recombinant NFAT1 (NFATp) is regulated by calcineurin in T cells and mediates transcription of several cytokine genes

Molecular and Cellular Biology, 1996-07, Vol.16 (7), p.3955-3966

1996

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T-cell receptor stimulation elicits an early phase of activation and a later phase of deactivation of the transcription factor NFAT1

Molecular and Cellular Biology, 1996-07, Vol.16 (7), p.3945-3954

1996

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Severe factor VII deficiency due to a mutation disrupting an Sp1 binding site in the factor VII promoter

Blood, 1998-09, Vol.92 (5), p.1639-1645

1998

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Characterization of Two Naturally Occurring Mutations in the Second Epidermal Growth Factor-Like Domain of Factor VII

Blood, 1999-02, Vol.93 (4), p.1237-1244

1999

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Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15-base pair insertion in the F7 gene

Blood, 2001-02, Vol.97 (4), p.960-965

2001

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The Effect of the B and Z DNA Conformations on the Introduction of Photodynamic Damage

Bioscience, 1983-12, Vol.33 (11), p.715-716

1983

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A new mutation in the HNF4 binding region of the factor VII promoter in a patient with severe factor VII deficiency

Blood, 2000-12, Vol.96 (13), p.4370-4372

2000

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Mechanism underlying factor VII deficiency in Jewish populations with the Ala 244 Val mutation

British journal of haematology, 1999-06, Vol.105 (4), p.1101-1108

1999

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Characterization of Two Naturally Occurring Mutations in the Second Epidermal Growth Factor-Like Domain of Factor VII

Blood, 1999-02, Vol.93 (4), p.1237-1244

1999

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Differential Myosin 5a splice variants in innervation of pelvic organs

Myosin 5a in the Urinary Bladder: Localization, Splice Variant Expression, and Functional Role in Neurotransmission

Myosin Va plays a role in nitrergic smooth muscle relaxation in gastric fundus and corpora cavernosa of penis

Upregulation of the coagulation factor VII gene during glucose deprivation is mediated by activating transcription factor 4

Expression of Myosin 5a splice variants in murine stomach

MP42-10 AUGMENTED BLADDER SMOOTH MUSCLE RESPONSIVENESS TO HYPERGLYCEMIA THROUGH A CAVEOLAE-DEPENDENT ACTIVATION OF RHO KINASE PATHWAY

MP42-14 PURINERGIC P2X4 RECEPTOR EXPRESSION AND FUNCTION IN RODENT BLADDER SMOOTH MUSCLE

Two naturally occurring mutations on FVII gene (S363I-W364C) altering intrinsic catalytic activity

Polymorphisms in the factor VII gene and ischemic stroke in young adults

CCAAT/Enhancer-binding Protein-β Participates in Insulin-responsive Expression of the Factor VII Gene

A new mutation in the HNF4 binding region of the factor VII promoter in a patient with severe factor VII deficiency

Severe Factor VII Deficiency Due to a Mutation Disrupting an Sp1 Binding Site in the Factor VII Promoter

Suppression of dimethylhydrazine-induced carcinogenesis in mice by dietary addition of the Bowman-Birk protease inhibitor

AB295. SPR-22 Functional relevance of purinergic P2X4R in bladder smooth muscle

Mechanism underlying factor VII deficiency in Jewish populations with the Ala244Val mutation

CCAAT/Enhancer-binding Protein-Î² Participates in Insulin-responsive Expression of the Factor VII Gene

Recombinant NFAT1 (NFATp) is regulated by calcineurin in T cells and mediates transcription of several cytokine genes

T-cell receptor stimulation elicits an early phase of activation and a later phase of deactivation of the transcription factor NFAT1

Severe factor VII deficiency due to a mutation disrupting an Sp1 binding site in the factor VII promoter

Characterization of Two Naturally Occurring Mutations in the Second Epidermal Growth Factor-Like Domain of Factor VII

Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15-base pair insertion in the F7 gene

The Effect of the B and Z DNA Conformations on the Introduction of Photodynamic Damage

A new mutation in the HNF4 binding region of the factor VII promoter in a patient with severe factor VII deficiency

Mechanism underlying factor VII deficiency in Jewish populations with the Ala 244 Val mutation

Characterization of Two Naturally Occurring Mutations in the Second Epidermal Growth Factor-Like Domain of Factor VII

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