Michael John Ackerman, MD, PhD, FACC

  • 34761 Citations
  • 103 Scopus h-Index
1991 …2020
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Research Output 1991 2019

2011
51 Citations (Scopus)

Unexplained drownings and the cardiac channelopathies: A molecular autopsy series

Tester, D. J., Medeiros-Domingo, A., Will, M. L. & Ackerman, M. J., 2011, In : Mayo Clinic Proceedings. 86, 10, p. 941-947 7 p.

Research output: Contribution to journalArticle

Channelopathies
Autopsy
Mutation
Long QT Syndrome
Ryanodine Receptor Calcium Release Channel
2010
13 Citations (Scopus)
Long QT Syndrome
Sympathectomy
Anesthesia
Anesthetics
Premedication
390 Citations (Scopus)

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Kapplinger, J. D., Tester, D. J., Alders, M., Benito, B., Berthet, M., Brugada, J., Brugada, P., Fressart, V., Guerchicoff, A., Harris-Kerr, C., Kamakura, S., Kyndt, F., Koopmann, T. T., Miyamoto, Y., Pfeiffer, R., Pollevick, G. D., Probst, V., Zumhagen, S., Vatta, M., Towbin, J. A. & 9 others, Shimizu, W., Schulze-Bahr, E., Antzelevitch, C., Salisbury, B. A., Guicheney, P., Wilde, A. A. M., Brugada, R., Schott, J. J. & Ackerman, M. J., Jan 2010, In : Heart Rhythm. 7, 1, p. 33-46 14 p.

Research output: Contribution to journalArticle

Brugada Syndrome
Sodium Channels
Genetic Testing
Mutation
Healthy Volunteers
19 Citations (Scopus)

A ZASP missense mutation, S196L, leads to cytoskeletal and electrical abnormalities in a mouse model of cardiomyopathy

Li, Z., Ai, T., Samani, K., Xi, Y., Tzeng, H. P., Xie, M., Wu, S., Ge, S., Taylor, M. D., Dong, J. W., Cheng, J., Ackerman, M. J., Kimura, A., Sinagra, G., Brunelli, L., Faulkner, G. & Vatta, M., Dec 2010, In : Circulation: Arrhythmia and Electrophysiology. 3, 6, p. 646-656 11 p.

Research output: Contribution to journalArticle

Dilated Cardiomyopathy
Missense Mutation
Cardiomyopathies
Sudden Cardiac Death
Mutation
38 Citations (Scopus)

Cardiac channel molecular autopsy for sudden unexpected death in epilepsy

Johnson, J. N., Tester, D. J., Bass, N. E. & Ackerman, M. J., 2010, In : Journal of Child Neurology. 25, 7, p. 916-921 6 p.

Research output: Contribution to journalArticle

Sudden Death
Autopsy
Epilepsy
Long QT Syndrome
Ryanodine Receptor Calcium Release Channel
270 Citations (Scopus)

Characteristics and clinical significance of late gadolinium enhancement by contrast-enhanced magnetic resonance imaging in patients with hypertrophic cardiomyopathy

Rubinshtein, R., Glockner, J., Ommen, S. R., Araoz, P. A., Ackerman, M. J., Sorajja, P., Bos, J. M., Tajik, A. J., Valeti, U. S., Nishimura, R. A. & Gersh, B. J., Jan 2010, In : Circulation: Heart Failure. 3, 1, p. 51-58 8 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Gadolinium
Magnetic Resonance Imaging
Sudden Cardiac Death
Defibrillators
172 Citations (Scopus)

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

Girolami, F., Ho, C. Y., Semsarian, C., Baldi, M., Will, M. L., Baldini, K., Torricelli, F., Yeates, L., Cecchi, F., Ackerman, M. J. & Olivotto, I., Apr 6 2010, In : Journal of the American College of Cardiology. 55, 14, p. 1444-1453 10 p.

Research output: Contribution to journalArticle

Sarcomeres
Hypertrophic Cardiomyopathy
Mutation
Proteins
Genes
55 Citations (Scopus)
Ion Channels
Cardiac Arrhythmias
Mutation
Genes
Proteins
27 Citations (Scopus)

Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation

Tester, D. J., Valdivia, C., Harris-Kerr, C., Alders, M., Salisbury, B. A., Wilde, A. A. M., Makielski, J. C. & Ackerman, M. J., Jul 2010, In : Heart Rhythm. 7, 7, p. 912-919 8 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Mutation
HEK293 Cells
Referral and Consultation
Sodium Channels
17 Citations (Scopus)

Exercise extreme caution when calling rare genetic variants novel arrhythmia syndrome susceptibility mutations

Wilde, A. A. M. & Ackerman, M. J., Dec 2010, In : Heart Rhythm. 7, 12, p. 1883-1885 3 p.

Research output: Contribution to journalArticle

Brugada Syndrome
Cardiac Electrophysiologic Techniques
Genetic Association Studies
Genetic Predisposition to Disease
Cardiac Arrhythmias
189 Citations (Scopus)

Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K ATP channel Kir6.1 as a pathogenic substrate for J-wave syndromes

Medeiros-Domingo, A., Tan, B. H., Crotti, L., Tester, D. J., Eckhardt, L., Cuoretti, A., Kroboth, S. L., Song, C., Zhou, Q., Kopp, D., Schwartz, P. J., Makielski, J. C. & Ackerman, M. J., Oct 2010, In : Heart Rhythm. 7, 10, p. 1466-1471 6 p.

Research output: Contribution to journalArticle

Adenosine Triphosphate
Brugada Syndrome
Mutation
KATP Channels
Missense Mutation
11 Citations (Scopus)

Gene-specific paradoxical QT responses during rapid eye movement sleep in women with congenital long QT syndrome

Lanfranchi, P. A., Ackerman, M. J., Kara, T., Shamsuzzaman, A. S. M., Wolk, R., Jurak, P., Amin, R. & Somers, V., 2010, In : Heart Rhythm. 7, 8, p. 1067-1074 8 p.

Research output: Contribution to journalArticle

Long QT Syndrome
REM Sleep
Sleep
Genes
Cardiac Arrhythmias

Genetics and Genomics of Hypertrophic Cardiomyopathy

Martijn Bos, J., Ommen, S. R. & Ackerman, M. J., 2010, Essentials of Genomic and Personalized Medicine. Elsevier Inc., p. 336-349 14 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Hypertrophic Cardiomyopathy
Genomics
Hypertrophy
Heart Failure
Syncope
3 Citations (Scopus)

Genetics of Heart Failure and Sudden Death

Vatta, M. & Ackerman, M. J., Oct 2010, In : Heart Failure Clinics. 6, 4, p. 507-514 8 p.

Research output: Contribution to journalArticle

Channelopathies
Long QT Syndrome
Penetrance
Sudden Cardiac Death
Sudden Death
32 Citations (Scopus)

Genomic risk factors in sudden infant death syndrome

Van Norstrand, D. W. & Ackerman, M. J., 2010, In : Genome Medicine. 2, 11, 86.

Research output: Contribution to journalArticle

Sudden Infant Death
Channelopathies
Infant Mortality
Nicotine
Energy Metabolism
65 Citations (Scopus)

Implantable cardioverter defibrillator therapy for congenital long QT syndrome: A single-center experience

Horner, J. M., Kinoshita, M., Webster, T. L., Haglund, C. M., Friedman, P. A. & Ackerman, M. J., Nov 2010, In : Heart Rhythm. 7, 11, p. 1616-1622 7 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Implantable Defibrillators
Therapeutics
Ventricular Fibrillation
Secondary Prevention
57 Citations (Scopus)

Loss-of-function mutation of the SCN3B-encoded sodium channel 3 subunit associated with a case of idiopathic ventricular fibrillation

Valdivia, C. R., Medeiros-Domingo, A., Ye, B., Shen, W. K., Algiers, T. J., Ackerman, M. J. & Makielski, J. C., Jun 2010, In : Cardiovascular Research. 86, 3, p. 392-400 9 p.

Research output: Contribution to journalArticle

Sodium Channels
Mutation
HEK293 Cells
COS Cells
Brugada Syndrome
21 Citations (Scopus)

Mutation-Specific Risk in Two Genetic Forms of Type 3 Long QT Syndrome

Liu, J. F., Moss, A. J., Jons, C., Benhorin, J., Schwartz, P. J., Spazzolini, C., Crotti, L., Ackerman, M. J., McNitt, S., Robinson, J. L., Qi, M., Goldenberg, I. & Zareba, W., Jan 15 2010, In : American Journal of Cardiology. 105, 2, p. 210-213 4 p.

Research output: Contribution to journalArticle

Mutation
Syncope
Long QT Syndrome
Parturition
Long QT syndrome type 3
94 Citations (Scopus)

Mutation type is not clinically useful in predicting prognosis in hypertrophic cardiomyopathy

Landstrom, A. P. & Ackerman, M. J., Dec 7 2010, In : Circulation. 122, 23, p. 2441-2449 9 p.

Research output: Contribution to journalArticle

Predictive Value of Tests
Hypertrophic Cardiomyopathy
Genotype
Mutation
46 Citations (Scopus)

Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing

Tester, D. J., Benton, A. J., Train, L., Deal, B., Baudhuin, L. M. & Ackerman, M. J., Oct 15 2010, In : American Journal of Cardiology. 106, 8, p. 1124-1128 5 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Genetic Testing
Syncope
Genes
Exons
255 Citations (Scopus)

Prevention of torsade de pointes in hospital settings: A scientific statement from the American heart association and the American college of cardiology foundation

Drew, B. J., Ackerman, M. J., Funk, M., Gibler, W. B., Kligfield, P., Menon, V., Philippides, G. J., Roden, D. M. & Zareba, W., Mar 2010, In : Circulation. 121, 8, p. 1047-1060 14 p.

Research output: Contribution to journalArticle

American Heart Association
Torsades de Pointes
Hospital Units
Electrophysiology
Physiologic Monitoring
164 Citations (Scopus)
International Nurses
Torsades de Pointes
Critical Care
Electrocardiography
Polyvinyl Chloride
13 Citations (Scopus)

Properties of WT and mutant hERG K+ channels expressed in neonatal mouse cardiomyocytes

Lin, E. C., Holzem, K. M., Anson, B. D., Moungey, B. M., Balijepalli, S. Y., Tester, D. J., Ackerman, M. J., Delisle, B. P., Balijepalli, R. C. & January, C. T., Jun 2010, In : American Journal of Physiology - Heart and Circulatory Physiology. 298, 6

Research output: Contribution to journalArticle

Cardiac Myocytes
Ether
Long QT Syndrome
Genes
Romano-Ward Syndrome

Response to Ho

Landstrom, A. P. & Ackerman, M. J., Dec 7 2010, In : Circulation. 122, 23, p. 2440 1 p.

Research output: Contribution to journalArticle

161 Citations (Scopus)

Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals

Goldenberg, I., Horr, S., Moss, A. J., Lopes, C. M., Barsheshet, A., McNitt, S., Zareba, W., Andrews, M. L., Robinson, J. L., Locati, E. H., Ackerman, M. J., Benhorin, J., Kaufman, E. S., Napolitano, C., Platonov, P. G., Priori, S. G., Qi, M., Schwartz, P. J., Shimizu, W., Towbin, J. A. & 3 others, Vincent, G. M., Wilde, A. A. M. & Zhang, L., Dec 28 2010, In : Journal of the American College of Cardiology. 57, 1, p. 51-59 9 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Reference Values
Genotype
Sudden Cardiac Death
Heart Arrest
68 Citations (Scopus)

Role of family history of sudden death in risk stratification and prevention of sudden death with implantable defibrillators in hypertrophic cardiomyopathy

Bos, J. M., Maron, B. J., Ackerman, M. J., Haas, T. S., Sorajja, P., Nishimura, R. A., Gersh, B. J. & Ommen, S. R., Nov 15 2010, In : American Journal of Cardiology. 106, 10, p. 1481-1486 6 p.

Research output: Contribution to journalArticle

Implantable Defibrillators
Hypertrophic Cardiomyopathy
Sudden Death
Primary Prevention
Ventricular Fibrillation
7 Citations (Scopus)

SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103Tyr

Killen, S. A. S., Kunic, J., Wang, L., Lewis, A., Levy, B. P., Ackerman, M. J. & George, A. L., May 14 2010, In : BMC Medical Genetics. 11, 1, 74.

Research output: Contribution to journalArticle

Allelic Imbalance
African Americans
Sudden Infant Death
Alleles
Sudden Death
81 Citations (Scopus)

Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

Tan, B. H., Pundi, K. N., Van Norstrand, D. W., Valdivia, C. R., Tester, D. J., Medeiros-Domingo, A., Makielski, J. C. & Ackerman, M. J., Jun 2010, In : Heart Rhythm. 7, 6, p. 771-778 8 p.

Research output: Contribution to journalArticle

Sudden Infant Death
Sodium Channels
Mutation
Channelopathies
Genes
4 Citations (Scopus)

The prevalence and diagnostic/prognostic utility of sinus arrhythmia in the evaluation of congenital long QT syndrome

Johnson, J. N. & Ackerman, M. J., Dec 2010, In : Heart Rhythm. 7, 12, p. 1785-1789 5 p.

Research output: Contribution to journalArticle

Sinus Arrhythmia
Long QT Syndrome
Andersen Syndrome
Romano-Ward Syndrome
Torsades de Pointes
6 Citations (Scopus)

Transient QT interval prolongation in an infant with Simpson-Golabi-Behmel syndrome

Gertsch, E., Kirmani, S., Ackerman, M. J. & Babovic-Vuksanovic, D., Sep 2010, In : American Journal of Medical Genetics, Part A. 152, 9, p. 2379-2382 4 p.

Research output: Contribution to journalArticle

Gigantism
Multiple Abnormalities
Long QT Syndrome
Congenital Heart Defects
Intellectual Disability
45 Citations (Scopus)

Trigger-specific risk factors and response to therapy in long QT syndrome type 2

Kim, J. A., Lopes, C. M., Moss, A. J., McNitt, S., Barsheshet, A., Robinson, J. L., Zareba, W., Ackerman, M. J., Kaufman, E. S., Towbin, J. A., Vincent, M. & Goldenberg, I., Dec 2010, In : Heart Rhythm. 7, 12, p. 1797-1805 9 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Arousal
Exercise
Mutation
Therapeutics
25 Citations (Scopus)

Z-Disc Genes in Hypertrophic Cardiomyopathy. Stretching the Cardiomyopathies?

Bos, J. M. & Ackerman, M. J., Mar 16 2010, In : Journal of the American College of Cardiology. 55, 11, p. 1136-1138 3 p.

Research output: Contribution to journalArticle

Familial Hypertrophic Cardiomyopathy
Microfilament Proteins
Hypertrophic Cardiomyopathy
Actin Cytoskeleton
Cardiomyopathies
2009
48 Citations (Scopus)

A functional and structural study of tropon in C mutations related to hypertrophic cardiomyopathy

Pinto, J. R., Parvatiyar, M. S., Jones, M. A., Liang, J., Ackerman, M. J. & Potter, J. D., Jul 10 2009, In : Journal of Biological Chemistry. 284, 28, p. 19090-19100 11 p.

Research output: Contribution to journalArticle

Troponin C
Hypertrophic Cardiomyopathy
Troponin
Mutation
Myosins
103 Citations (Scopus)

Cardiac Ankyrin Repeat Protein Gene (ANKRD1) Mutations in Hypertrophic Cardiomyopathy

Arimura, T., Bos, J. M., Sato, A., Kubo, T., Okamoto, H., Nishi, H., Harada, H., Koga, Y., Moulik, M., Doi, Y. L., Towbin, J. A., Ackerman, M. J. & Kimura, A., Jul 21 2009, In : Journal of the American College of Cardiology. 54, 4, p. 334-342 9 p.

Research output: Contribution to journalArticle

Ankyrin Repeat
Connectin
Hypertrophic Cardiomyopathy
Mutation
Proteins
85 Citations (Scopus)

Cardiomyopathic and channelopathic causes of sudden unexplained death in infants and children

Tester, D. J. & Ackerman, M. J., 2009, In : Annual Review of Medicine. 60, p. 69-84 16 p.

Research output: Contribution to journalArticle

Sudden Death
Channelopathies
Autopsy
Testing
Arrhythmogenic Right Ventricular Dysplasia
55 Citations (Scopus)

Clinical Implications for Patients With Long QT Syndrome Who Experience a Cardiac Event During Infancy

Spazzolini, C., Mullally, J., Moss, A. J., Schwartz, P. J., McNitt, S., Ouellet, G., Fugate, T., Goldenberg, I., Jons, C., Zareba, W., Robinson, J. L., Ackerman, M. J., Benhorin, J., Crotti, L., Kaufman, E. S., Locati, E. H., Qi, M., Napolitano, C., Priori, S. G., Towbin, J. A. & 1 others, Vincent, G. M., Aug 25 2009, In : Journal of the American College of Cardiology. 54, 9, p. 832-837 6 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Heart Arrest
Sudden Cardiac Death
Syncope
Heart Rate
96 Citations (Scopus)

Device complications and inappropriate implantable cardioverter defibrillator shocks in patients with hypertrophic cardiomyopathy

Lin, G. D., Nishimura, R. A., Gersh, B. J., Phil, D., Ommen, S. R., Ackerman, M. J. & Brady, P. A., May 2009, In : Heart. 95, 9, p. 709-714 6 p.

Research output: Contribution to journalArticle

Implantable Defibrillators
Hypertrophic Cardiomyopathy
Shock
Equipment and Supplies
Atrial Fibrillation
236 Citations (Scopus)

Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy

Bos, J. M., Towbin, J. A. & Ackerman, M. J., Jul 14 2009, In : Journal of the American College of Cardiology. 54, 3, p. 201-211 11 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Genetic Testing
Therapeutics
Medicine
Genetic Association Studies
20 Citations (Scopus)

Diastolic Dysfunction and Its Histopathological Correlation in Obstructive Hypertrophic Cardiomyopathy in Children and Adolescents

Menon, S. C., Eidem, B. W., Dearani, J. A., Ommen, S. R., Ackerman, M. J. & Miller, D., Dec 2009, In : Journal of the American Society of Echocardiography. 22, 12, p. 1327-1334 8 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Muscle Cells
Fibrosis
Hypertrophy
Left Ventricular Dysfunction
16 Citations (Scopus)

Expression patterns of cardiac myofilament proteins

Theis, J. L., Bos, J. M., Theis, J. D., Miller, D. V., Dearani, J. A., Schaff, H. V., Gersh, B. J., Ommen, S. R., Moss, R. L. & Ackerman, M. J., Jul 2009, In : Circulation: Heart Failure. 2, 4, p. 325-333 9 p.

Research output: Contribution to journalArticle

Myofibrils
Hypertrophic Cardiomyopathy
Proteins
Mutation
Sarcomeres
237 Citations (Scopus)

Genetic testing for long-qt syndrome: Distinguishing pathogenic mutations from benign variants

Kapa, S., Tester, D. J., Salisbury, B. A., Harris-Kerr, C., Pungliya, M. S., Alders, M., Wilde, A. A. M. & Ackerman, M. J., Nov 2009, In : Circulation. 120, 18, p. 1752-1760 9 p.

Research output: Contribution to journalArticle

Genetic Testing
Mutation
Long QT Syndrome
Missense Mutation
Virulence
164 Citations (Scopus)

Genotype-Phenotype Aspects of Type 2 Long QT Syndrome

Shimizu, W., Moss, A. J., Wilde, A. A. M., Towbin, J. A., Ackerman, M. J., January, C. T., Tester, D. J., Zareba, W., Robinson, J. L., Qi, M., Vincent, G. M., Kaufman, E. S., Hofman, N., Noda, T., Kamakura, S., Miyamoto, Y., Shah, S., Amin, V., Goldenberg, I., Andrews, M. L. & 1 others, McNitt, S., Nov 24 2009, In : Journal of the American College of Cardiology. 54, 22, p. 2052-2062 11 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Genotype
Phenotype
Mutation
Missense Mutation
72 Citations (Scopus)
Brugada Syndrome
Sudden Infant Death
Sodium Channels
Oxidation-Reduction
Phosphorylation
5 Citations (Scopus)

GWAS or Gee Whiz, PSAS or Pshaw: Elucidating the biologic and clinical significance of genetic variation in cardiovascular disease

Landstrom, A. P. & Ackerman, M. J., Dec 2009, In : Heart Rhythm. 6, 12, p. 1751-1753 3 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Sudden Cardiac Death
Single Nucleotide Polymorphism
Coronary Artery Disease
Cardiovascular Diseases
22 Citations (Scopus)

Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutations

McLeod, C. J., Bos, J. M., Theis, J. L., Edwards, W. D., Gersh, B. J., Ommen, S. R. & Ackerman, M. J., Nov 2009, In : American Heart Journal. 158, 5, p. 799-805 7 p.

Research output: Contribution to journalArticle

Myofibrils
Hypertrophic Cardiomyopathy
Renin-Angiotensin System
Mutation
Muscle Cells

Hypertrophic Cardiomyopathy in the Era of Genomic Medicine

Bos, J. M., Ommen, S. R. & Ackerman, M. J., 2009, Genomic and Personalized Medicine, Two-Vol Set. Elsevier Inc., p. 716-728 13 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Hypertrophic Cardiomyopathy
Medicine
162 Citations (Scopus)

Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy

Johnson, J. N., Hofman, N., Haglund, C. M., Cascino, G. D., Wilde, A. A. M. & Ackerman, M. J., Jan 20 2009, In : Neurology. 72, 3, p. 224-231 8 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Epilepsy
Seizures
Phenotype
Anticonvulsants
212 Citations (Scopus)

Left cardiac sympathetic denervation for the treatment of long QT syndrome and catecholaminergic polymorphic ventricular tachycardia using video-assisted thoracic surgery

Collura, C. A., Johnson, J. N., Moir, C. & Ackerman, M. J., Jun 2009, In : Heart Rhythm. 6, 6, p. 752-759 8 p.

Research output: Contribution to journalArticle

Video-Assisted Thoracic Surgery
Long QT Syndrome
Sympathectomy
Secondary Prevention
Primary Prevention
17 Citations (Scopus)

Long QT syndrome due to a novel mutation in SCN5A: Treatment with ICD placement at 1 month and left cardiac sympathetic denervation at 3 months of age

Silver, E. S., Liberman, L., Chung, W. K., Spotnitz, H. M., Chen, J. M., Ackerman, M. J., Moir, C., Hordof, A. J. & Pass, R. H., Oct 2009, In : Journal of Interventional Cardiac Electrophysiology. 26, 1, p. 41-45 5 p.

Research output: Contribution to journalArticle

Torsades de Pointes
Long QT Syndrome
Sympathectomy
Mutation
Newborn Infant
49 Citations (Scopus)

Molecular evolution of the junctophilin gene family

Garbino, A., Van Oort, R. J., Dixit, S. S., Landstrom, A. P., Ackerman, M. J. & Wehrens, X. H. T., May 2009, In : Physiological Genomics. 37, 3, p. 175-186 12 p.

Research output: Contribution to journalArticle

Molecular Evolution
Genes
Calcium Channels
Membranes
Protein Isoforms