Robert H. Jr. Brown
#183,083
Most Influential Person Now
Robert H. Jr. Brown's AcademicInfluence.com Rankings
Robert H. Jr. Brownbiology Degrees
Biology
#15355
World Rank
#19314
Historical Rank
Molecular Biology
#2636
World Rank
#2677
Historical Rank
Biochemistry
#2697
World Rank
#2880
Historical Rank
Download Badge
Biology
Why Is Robert H. Jr. Brown Influential?
(Suggest an Edit or Addition)Robert H. Jr. Brown's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Dystrophin: The protein product of the duchenne muscular dystrophy locus (1987) (4384)
- Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury (1996) (1314)
- Mutant dynactin in motor neuron disease (2003) (962)
- Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy (1998) (841)
- Dysferlin Interacts with Annexins A1 and A2 and Mediates Sarcolemmal Wound-healing* (2003) (369)
- Inhibition of ICE slows ALS in mice (1997) (343)
- T lymphocytes potentiate endogenous neuroprotective inflammation in a mouse model of ALS (2008) (317)
- A Met-to-Val mutation in the skeletal muscle Na+ channel α-subunit in hyperkalaemic periodic paralysis (1991) (309)
- Targeting Nrf2 Signaling Improves Bacterial Clearance by Alveolar Macrophages in Patients with COPD and in a Mouse Model (2011) (282)
- Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis (2010) (254)
- Neonatal Neuronal Circuitry Shows Hyperexcitable Disturbance in a Mouse Model of the Adult-Onset Neurodegenerative Disease Amyotrophic Lateral Sclerosis (2008) (223)
- Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita (1992) (213)
- A sodium channel defect in hyperkalemic periodic paralysis: Potassium-induced failure of inactivation (1991) (195)
- Dysferlin in Membrane Trafficking and Patch Repair (2007) (148)
- Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel (1992) (146)
- Decreased pulmonary vascular permeability in aquaporin-1-null humans (2002) (113)
- Tetanus toxin C fragment-conjugated nanoparticles for targeted drug delivery to neurons. (2007) (95)
- Toxic mutants in Charcot's sclerosis (1995) (69)
- Postischemic Infusion of Cu/Zn Superoxide Dismutase or SOD:Tet451 Reduces Cerebral Infarction Following Focal Ischemia/Reperfusion in Rats (1997) (67)
- Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis (1995) (62)
- Methylprednisolone increases dystrophin levels by inhibiting myotube death during myogenesis of normal human muscle in vitro (1991) (59)
- SOD1 aggregates in ALS: Cause, correlate or consequence? (1998) (57)
- VEGF increases blood–brain barrier permeability to Evans blue dye and tetanus toxin fragment C but not adeno-associated virus in ALS mice (2008) (51)
- ATF3 expression improves motor function in the ALS mouse model by promoting motor neuron survival and retaining muscle innervation (2014) (48)
- A glial cell line-derived neurotrophic factor (GDNF):tetanus toxin fragment C protein conjugate improves delivery of GDNF to spinal cord motor neurons in mice (2006) (46)
- Hypokalemic periodic paralysis mutations: Confirmation of mutation and analysis of founder effect (1996) (42)
- Molecular biology of Duchenne muscular dystrophy (1988) (33)
- A survival motor neuron:tetanus toxin fragment C fusion protein for the targeted delivery of SMN protein to neurons (2004) (29)
- Different gene loci for hyperkalemic and hypokalemic periodic paralysis (1991) (26)
- IGF-1:Tetanus toxin fragment C fusion protein improves delivery of IGF-1 to spinal cord but fails to prolong survival of ALS mice (2009) (24)
- Heteroplasmy in Chronic External Ophthalmoplegia: Clinical and Molecular Observations (1990) (22)
- Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes (2006) (20)
- Insect GDNF:TTC fusion protein improves delivery of GDNF to mouse CNS. (2009) (17)
- Putting the heat on ALS (2004) (15)
- Proteolytic fragment or new gene product? (1988) (13)
- Molecular genetic analysis of dysferlin in Japanese patients with Miyoshi myopathy (1999) (12)
- A novel mutation in the spastin gene in a family with spastic paraplegia (2002) (12)
- Ion Channel Mutations in Periodic Paralysis and Related Myotonic Diseases a (1993) (9)
- Serum Nogo-A levels are not elevated in amyotrophic lateral sclerosis patients (2009) (9)
- Restrictive Lung Disease in the Cu/Zn Superoxide-Dismutase 1 G93A Amyotrophic Lateral Sclerosis Mouse Model. (2017) (8)
- Polyubiquitin Gene Expression following Cerebral Ischemia a (1993) (8)
- Neuron Research Leaps Ahead (2008) (4)
- Recombinant GDNF: tetanus toxin fragment C fusion protein produced from insect cells. (2009) (3)
- Glucocorticoids increase myoblast proliferation rates by inhibiting death of cycling cells (1991) (3)
- Harvey Macrophages in Patients with COPD and in a Mouse Model Targeting Nrf 2 Signaling Improves Bacterial Clearance by Alveolar (2011) (3)
- Chapter 112 – Myotonia and Periodic Paralysis (2003) (2)
- Genetics of neuromuscular disorders edited by Christos S. Bartsocas, Alan R. Liss, 1989. $84.00 (230 pages) ISBN 0 8451 5156 8 (1990) (2)
- Effects Of Obesity On Airway Architecture Based On Asthma Status (2011) (1)
- Molecular Genetics of ALS (2015) (0)
- Activation and Modulation of the ICE Aapoptosis Gene in ALS, a Novel Therapeutic Intervention.: 783 (1997) (0)
- Molecular Investigation of LGMD2B-Haplotype Analysis and Mutation Screening (2001) (0)
- S-6-4 Myotonia and periodic paralysis: implications of molecular defects for treatment (1995) (0)
- Genetic determinants of cerebral edema in severe traumatic brain injury: A pilot study of the role of CACNA1 and AQP4 gene mutations (2012) (0)
- Hepatoprotective biomarkers, amphiregulin and soluble Fas, increase during ELAD treatment in alcoholic hepatitis subjects (2018) (0)
- Pulmonary Function And Markers Of Systemic Inflammation And Oxidative Stress (2011) (0)
- Theoretical Reconstruction ofMyotonia andParalysis Causedby Incomplete Inactivation ofSodiumChannels (1993) (0)
- F.108. T Lymphocytes Potentiate Endogenous Neuroprotective Inflammation in a Mouse Model of ALS (2008) (0)
- Enhancing Nrf2 By Sulforaphane Improve Bacterial Phagocytosis By COPD Macrophages And Reduces Bacterial Exacerbations In Cigarette Smoke-Exposed Mice (2012) (0)
- Affect AMPA/Kainate Currents the Maturation of NMDA Currents, but Does Not Chronic NMDA Receptor Blockade From Birth Delays (2015) (0)
- Title Mutations in Potassium Channel Kir 2 . 6 Cause Susceptibility toThyrotoxic Hypokalemic Periodic Paralysis (2010) (0)
- aquaporin-1 -null humans (2016) (0)
This paper list is powered by the following services:
What Schools Are Affiliated With Robert H. Jr. Brown?
Robert H. Jr. Brown is affiliated with the following schools:
