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T Reynolds

Showing results (371-380 of 433) with videos related to

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Molecular Biology and Evolution|May 2, 2017
Differential Retention of Gene Functions in a Secondary Metabolite ClusterHannah T Reynolds, Jason C Slot, Hege H Divon, et al.
Human Mutation|April 17, 1999
Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. OnlineK J Norrgard, R J Pomponio, K L Swango, et al.
Catheterization and Cardiovascular Diagnosis|March 1, 1996
Subclavian vein anatomic subtypes defined by digital cinefluroscopic venography prior to permanent pacemaker lead insertionD E Smith, T M Doherty, G T Reynolds, et al.
Equine Veterinary Journal|October 1, 1977
The value of arterial blood pressure measurement in assessing the prognosis in equine colicC C Gay, J Carter, M McCarthy, et al.
Human Gene Therapy|June 10, 1996
A phase I study of an adeno-associated virus-CFTR gene vector in adult CF patients with mild lung diseaseT Flotte, B Carter, C Conrad, et al.
Pharmacology and Therapeutics in Dentistry|January 1, 1980
Anticaries and antiplaque potential of free-fatty acids in vitro and in vivoG S Schuster, T R Dirksen, A E Ciarlone, et al.
British Medical Journal|August 5, 1978
Antibodies to Yersinia enterocolitica serotype 3 in thyroid diseaseM T Reynolds, C T Keane, G H Tomkin, et al.
Science (New York, N.Y.)|August 4, 2012
A 200-second quasi-periodicity after the tidal disruption of a star by a dormant black holeR C Reis, J M Miller, M T Reynolds, et al.
Lancet (London, England)|September 12, 1998
Efficient and persistent gene transfer of AAV-CFTR in maxillary sinusJ A Wagner, T Reynolds, M L Moran, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Quantitative Magnetic Resonance Cerebral Spinal Fluid Flow Properties and Executive Function Cognitive Outcomes in Congenital Heart DiseaseVincent Kyu Lee, William T Reynolds, Julia Wallace, et al.
Pageof 44

Showing results (371-380 of 433) with videos related to

Sort By:
Pageof 44
Molecular Biology and Evolution|May 2, 2017
Differential Retention of Gene Functions in a Secondary Metabolite ClusterHannah T Reynolds, Jason C Slot, Hege H Divon, et al.
Human Mutation|April 17, 1999
Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. OnlineK J Norrgard, R J Pomponio, K L Swango, et al.
Catheterization and Cardiovascular Diagnosis|March 1, 1996
Subclavian vein anatomic subtypes defined by digital cinefluroscopic venography prior to permanent pacemaker lead insertionD E Smith, T M Doherty, G T Reynolds, et al.
Equine Veterinary Journal|October 1, 1977
The value of arterial blood pressure measurement in assessing the prognosis in equine colicC C Gay, J Carter, M McCarthy, et al.
Human Gene Therapy|June 10, 1996
A phase I study of an adeno-associated virus-CFTR gene vector in adult CF patients with mild lung diseaseT Flotte, B Carter, C Conrad, et al.
Pharmacology and Therapeutics in Dentistry|January 1, 1980
Anticaries and antiplaque potential of free-fatty acids in vitro and in vivoG S Schuster, T R Dirksen, A E Ciarlone, et al.
British Medical Journal|August 5, 1978
Antibodies to Yersinia enterocolitica serotype 3 in thyroid diseaseM T Reynolds, C T Keane, G H Tomkin, et al.
Science (New York, N.Y.)|August 4, 2012
A 200-second quasi-periodicity after the tidal disruption of a star by a dormant black holeR C Reis, J M Miller, M T Reynolds, et al.
Lancet (London, England)|September 12, 1998
Efficient and persistent gene transfer of AAV-CFTR in maxillary sinusJ A Wagner, T Reynolds, M L Moran, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Quantitative Magnetic Resonance Cerebral Spinal Fluid Flow Properties and Executive Function Cognitive Outcomes in Congenital Heart DiseaseVincent Kyu Lee, William T Reynolds, Julia Wallace, et al.
Pageof 44