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TikTok Extends the Wasteland

The Hedgehog review, 2023-07, Vol.25 (2)

Hewitt, Jeff

2023

Volltextzugriff (PDF)

Somatostatin receptor subtype expression and function in human vascular tissue

American journal of physiology. Heart and circulatory physiology, 2000-06, Vol.278 (6), p.H1815-H1822

2000

Volltextzugriff (PDF)

Regulation of granuloma formation via Myd88 and Nox2 in a model of pulmonary sarcoidosis (MPF5P.741)

The Journal of immunology (1950), 2015-05, Vol.194 (1_Supplement), p.137-137.4

2015

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Biomining with bacteriophage: Selectivity of displayed peptides for naturally occurring sphalerite and chalcopyrite

Biotechnology and bioengineering, 2009-02, Vol.102 (2), p.644-650

2009

Volltextzugriff (PDF)

Identification and Cloning of Novel Mutations In a Compound Heterozygous Factor V Deficient Patient

Blood, 2010-11, Vol.116 (21), p.2210-2210

2010

Volltextzugriff (PDF)

Novel Compound Heterozygous Factor V Deficiency with Severe Clinical Phenotype

Blood, 2009-11, Vol.114 (22), p.3490-3490

2009

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A novel compensating mechanism for homozygous coagulation factor V deficiency suggested by enhanced activated partial thromboplastin time after reconstitution with normal factor V

British journal of haematology, 2010-10, Vol.151 (2), p.198-200

2010

Volltextzugriff (PDF)

Differential Effect of a His Tag at the N- and C-Termini: Functional Studies with Recombinant Human Serum Transferrin

Biochemistry (Easton), 2002-07, Vol.41 (30), p.9448-9454

2002

Volltextzugriff (PDF)

Engineering the Primary Substrate Specificity of Streptomyces griseus Trypsin

Biochemistry (Easton), 2003-08, Vol.42 (30), p.9060-9066

2003

Volltextzugriff (PDF)

Molecular determination of the breakpoints of a 161 556 bp deletion at chromosome 13q34 that presented as severe factor VII deficiency in a neonate

British journal of haematology, 2008-03, Vol.140 (5), p.589-592

2008

Volltextzugriff (PDF)

Germline mutation identified after amplification of nuclear DNA from citrated plasma

British journal of haematology, 2007-01, Vol.136 (1), p.171-172

2007

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Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion

British journal of haematology, 2005-02, Vol.128 (3), p.380-385

2005

Volltextzugriff (PDF)

Cloning, mutagenesis, and structural analysis of human pancreatic α-amylase expressed in Pichia pastoris

Protein science, 1999-03, Vol.8 (3), p.635-643

1999

Volltextzugriff (PDF)

Identification of the epitope of a monoclonal antibody that disrupts binding of human transferrin to the human transferrin receptor

The FEBS journal, 2005-12, Vol.272 (24), p.6344-6353

2005

Volltextzugriff (PDF)

What's really slowing your digital transformation?

Logistics Management (2002), 2020-04, Vol.59 (4), p.18-20

2020

Volltextzugriff (PDF)

What's really slowing your digital transformation?

Supply Chain Management Review, 2020-03, Vol.24 (2), p.60-62

2020

Volltextzugriff (PDF)

Confirmation of paternity suggests a new mutation in the factor VII gene: ‘Pater certus quouque est’ ‐ Response to Girolami et al

British journal of haematology, 2005-08, Vol.130 (3), p.459-460

2005

Volltextzugriff (PDF)

Somatostatin receptor subtype expression and function in human vascular tissue

American journal of physiology. Heart and circulatory physiology, 2000-06, Vol.47 (6), p.H1815-H1822

2000

Volltextzugriff (PDF)

Effect of endothelial and adventitial injury on somatostatin receptor expression

Surgery, 2000-05, Vol.127 (5), p.577-583

2000

Volltextzugriff (PDF)

The role of data, analytics and insights in health care

Chain drug review, 2016-08, p.14

Hewitt, Jeff

2016

Volltextzugriff (PDF)

Equus caballus gelsolin

European journal of biochemistry, 1998-02, Vol.251 (3), p.613-621

1998

Volltextzugriff (PDF)

Nucleotide sequence of the phosphotransacetylase gene of Escherichia coli strain K12

Biochimica et biophysica acta, 1994-10, Vol.1219 (2), p.559-562

1994

Volltextzugriff (PDF)

Equus caballus gelsolin cDNA sequence and protein structural implications

European journal of biochemistry, 1998-02, Vol.251 (3), p.613-621

1998

Volltextzugriff (PDF)

Isolation of a murine glucose-dependent insulinotropic polypeptide (GIP) cDNA from a tumor cell line (STC6-14) and quantification of glucose-induced increases in GIP mRNA

Biochimica et biophysica acta, 1996-08, Vol.1308 (2), p.111-113

1996

Volltextzugriff (PDF)

A novel compensating mechanism for homozygous coagulation factor V deficiency suggested by enhanced activated partial thromboplastin time after reconstitution with normal factor V

British journal of haematology, 2010, Vol.151 (2), p.198-200

2010

Volltextzugriff (PDF)

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TikTok Extends the Wasteland

Somatostatin receptor subtype expression and function in human vascular tissue

Regulation of granuloma formation via Myd88 and Nox2 in a model of pulmonary sarcoidosis (MPF5P.741)

Biomining with bacteriophage: Selectivity of displayed peptides for naturally occurring sphalerite and chalcopyrite

Identification and Cloning of Novel Mutations In a Compound Heterozygous Factor V Deficient Patient

Novel Compound Heterozygous Factor V Deficiency with Severe Clinical Phenotype

A novel compensating mechanism for homozygous coagulation factor V deficiency suggested by enhanced activated partial thromboplastin time after reconstitution with normal factor V

Differential Effect of a His Tag at the N- and C-Termini: Functional Studies with Recombinant Human Serum Transferrin

Engineering the Primary Substrate Specificity of Streptomyces griseus Trypsin

Molecular determination of the breakpoints of a 161 556 bp deletion at chromosome 13q34 that presented as severe factor VII deficiency in a neonate

Germline mutation identified after amplification of nuclear DNA from citrated plasma

Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion

Cloning, mutagenesis, and structural analysis of human pancreatic α-amylase expressed in Pichia pastoris

Identification of the epitope of a monoclonal antibody that disrupts binding of human transferrin to the human transferrin receptor

What's really slowing your digital transformation?

What's really slowing your digital transformation?

Confirmation of paternity suggests a new mutation in the factor VII gene: ‘Pater certus quouque est’ ‐ Response to Girolami et al

Somatostatin receptor subtype expression and function in human vascular tissue

Effect of endothelial and adventitial injury on somatostatin receptor expression

The role of data, analytics and insights in health care

Equus caballus gelsolin

Nucleotide sequence of the phosphotransacetylase gene of Escherichia coli strain K12

Equus caballus gelsolin cDNA sequence and protein structural implications

Isolation of a murine glucose-dependent insulinotropic polypeptide (GIP) cDNA from a tumor cell line (STC6-14) and quantification of glucose-induced increases in GIP mRNA

A novel compensating mechanism for homozygous coagulation factor V deficiency suggested by enhanced activated partial thromboplastin time after reconstitution with normal factor V

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