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Genomics
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March 1, 1996
Molecular cloning and chromosomal localization of the human cyclin C (CCNC) and cyclin E (CCNE) genes: deletion of the CCNC gene in human tumors
H Li, J M Lahti, M Valentine, et al.
Neurobiology of Aging
|
December 21, 2018
Selective reduction of APP-BACE1 activity improves memory via NMDA-NR2B receptor-mediated mechanisms in aged PDAPP mice
Charles E Evans, Rhian S Thomas, Thomas J Freeman, et al.
Clinical Radiology
|
September 4, 2007
Primary ciliary dyskinesia in the paediatric population: range and severity of radiological findings in a cohort of patients receiving tertiary care
K Jain, S P G Padley, E J Goldstraw, et al.
European Journal of Pharmacology
|
July 20, 2010
TPI 1020, a novel anti-inflammatory, nitric oxide donating compound, potentiates the bronchodilator effects of salbutamol in conscious guinea-pigs
Dawn L Turner, Nicolay Ferrari, William R Ford, et al.
Gynecologic Oncology
|
February 27, 2004
Occult cancer of the fallopian tube in a BRCA2 germline mutation carrier at prophylactic salpingo-oophorectomy
A R McEwen, D T McConnell, D N Kenwright, et al.
Medical Education
|
May 25, 2005
Blurring the boundaries: scenario-based simulation in a clinical setting
R L Kneebone, J Kidd, D Nestel, et al.
Genome Announcements
|
April 18, 2015
Whole-Genome Sequences of Five Burkholderia pseudomallei Isolates from Australian Cystic Fibrosis Patients
Linda T Viberg, Erin P Price, Timothy J Kidd, et al.
The Journal of Biological Chemistry
|
November 16, 2001
PITSLRE p110 protein kinases associate with transcription complexes and affect their activity
Janeen H Trembley, Dongli Hu, Li-Chung Hsu, et al.
Thorax
|
December 3, 2003
Burkholderia pseudomallei: another emerging pathogen in cystic fibrosis
M R O'Carroll, T J Kidd, C Coulter, et al.
Pediatric Blood & Cancer
|
October 24, 2009
Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene
B Kanathezhath, F K Hazard, H Guo, et al.
Page
of 41
Search research articles
Search
Showing results (241-250 of 403) with videos related to
Sort By:
Page
of 41
Genomics
|
March 1, 1996
Molecular cloning and chromosomal localization of the human cyclin C (CCNC) and cyclin E (CCNE) genes: deletion of the CCNC gene in human tumors
H Li, J M Lahti, M Valentine, et al.
Neurobiology of Aging
|
December 21, 2018
Selective reduction of APP-BACE1 activity improves memory via NMDA-NR2B receptor-mediated mechanisms in aged PDAPP mice
Charles E Evans, Rhian S Thomas, Thomas J Freeman, et al.
Clinical Radiology
|
September 4, 2007
Primary ciliary dyskinesia in the paediatric population: range and severity of radiological findings in a cohort of patients receiving tertiary care
K Jain, S P G Padley, E J Goldstraw, et al.
European Journal of Pharmacology
|
July 20, 2010
TPI 1020, a novel anti-inflammatory, nitric oxide donating compound, potentiates the bronchodilator effects of salbutamol in conscious guinea-pigs
Dawn L Turner, Nicolay Ferrari, William R Ford, et al.
Gynecologic Oncology
|
February 27, 2004
Occult cancer of the fallopian tube in a BRCA2 germline mutation carrier at prophylactic salpingo-oophorectomy
A R McEwen, D T McConnell, D N Kenwright, et al.
Medical Education
|
May 25, 2005
Blurring the boundaries: scenario-based simulation in a clinical setting
R L Kneebone, J Kidd, D Nestel, et al.
Genome Announcements
|
April 18, 2015
Whole-Genome Sequences of Five Burkholderia pseudomallei Isolates from Australian Cystic Fibrosis Patients
Linda T Viberg, Erin P Price, Timothy J Kidd, et al.
The Journal of Biological Chemistry
|
November 16, 2001
PITSLRE p110 protein kinases associate with transcription complexes and affect their activity
Janeen H Trembley, Dongli Hu, Li-Chung Hsu, et al.
Thorax
|
December 3, 2003
Burkholderia pseudomallei: another emerging pathogen in cystic fibrosis
M R O'Carroll, T J Kidd, C Coulter, et al.
Pediatric Blood & Cancer
|
October 24, 2009
Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene
B Kanathezhath, F K Hazard, H Guo, et al.
Page
of 41