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Glycomic and glycotranscriptomic profiling of mucin-type O-glycans in planarian Schmidtea mediterranea

Glycobiology (Oxford), 2022-02, Vol.32 (1), p.36-49

2022

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Fixation of deleterious mutations at critical positions in human proteins

Molecular biology and evolution, 2011-09, Vol.28 (9), p.2687-2693

Subramanian, Sankar

2011

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Temporal Trails of Natural Selection in Human Mitogenomes

Molecular biology and evolution, 2009-04, Vol.26 (4), p.715-717

Subramanian, Sankar

2009

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The Codon Statistics Database: A Database of Codon Usage Bias

Molecular biology and evolution, 2022-08, Vol.39 (8)

2022

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Temporal patterns of fruit fly (Drosophila) evolution revealed by mutation clocks

Molecular biology and evolution, 2004-01, Vol.21 (1), p.36-44

2004

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High proportions of deleterious polymorphisms in constrained human genes

Molecular biology and evolution, 2011-01, Vol.28 (1), p.49-52

Subramanian, Sankar

2011

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Human angiogenin is a neuroprotective factor and amyotrophic lateral sclerosis associated angiogenin variants affect neurite extension/pathfinding and survival of motor neurons

Human molecular genetics, 2008-01, Vol.17 (1), p.130-149

2008

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Hippocampals neurogenesis is impaired in mice with a deletion in the coiled coil domain of Talpid3—implications for Joubert syndrome

Human molecular genetics, 2022-09, Vol.31 (19), p.3245-3265

2022

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A new role for angiogenin in neurite growth and pathfinding: implications for amyotrophic lateral sclerosis

Human molecular genetics, 2007-06, Vol.16 (12), p.1445-1453

2007

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Adaptive Capacity of a DNA Polymerase Clamp-loader ATPase Complex

Molecular biology and evolution, 2024-03, Vol.41 (3)

2024

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Lack of exacerbation of neurodegeneration in a double transgenic mouse model of mutant LRRK2 and tau

Human molecular genetics, 2015-06, Vol.24 (12), p.3545-3556

2015

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Recapitulating Evolutionary Divergence in a Single Cis-Regulatory Element Is Sufficient to Cause Expression Changes of the Lens Gene Tdrd7

Molecular biology and evolution, 2021-02, Vol.38 (2), p.380-392

2021

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Higher intensity of purifying selection on >90% of the human genes revealed by the intrinsic replacement mutation rates

Molecular biology and evolution, 2006-12, Vol.23 (12), p.2283-2287

2006

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Prevalence of the F-type lectin domain

Glycobiology (Oxford), 2015-08, Vol.25 (8), p.888-901

2015

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Patterns of transitional mutation biases within and among mammalian genomes

Molecular biology and evolution, 2003-06, Vol.20 (6), p.988-993

2003

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Role of Na(v)1.9 in activity-dependent axon growth in motoneurons

Human molecular genetics, 2012-08, Vol.21 (16), p.3655-3667

2012

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Thermodynamic binding studies of bivalent oligosaccharides to galectin-1, galectin-3, and the carbohydrate recognition domain of galectin-3

Glycobiology (Oxford), 2004-09, Vol.14 (9), p.817-825

2004

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Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies

Human molecular genetics, 2015-07, Vol.24 (14), p.3994-4005

2015

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Signatures of ecological resource availability in the animal and plant proteomes

Molecular biology and evolution, 2006-10, Vol.23 (10), p.1946-1951

2006

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Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6

Human molecular genetics, 2009-02, Vol.18 (3), p.535-545

2009

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Peanut lectin stimulates proliferation of colon cancer cells by interaction with glycosylated CD44v6 isoforms and consequential activation of c-Met and MAPK: functional implications for disease-associated glycosylation changes

Glycobiology (Oxford), 2006-07, Vol.16 (7), p.594-601

2006

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Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6

Human molecular genetics, 2009-04, Vol.18 (8), p.1544-1544

2009

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Linkage analysis conditional on HLA status in a large north american pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12

Human molecular genetics, 2002-02, Vol.11 (3), p.295-300

2002

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Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith—Wiedemann syndrome

Human molecular genetics, 1995-03, Vol.4 (3), p.395-399

1995

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Glycomic and glycotranscriptomic profiling of mucin-type O-glycans in planarian Schmidtea mediterranea

Fixation of deleterious mutations at critical positions in human proteins

Temporal Trails of Natural Selection in Human Mitogenomes

The Codon Statistics Database: A Database of Codon Usage Bias

Temporal patterns of fruit fly (Drosophila) evolution revealed by mutation clocks

High proportions of deleterious polymorphisms in constrained human genes

Human angiogenin is a neuroprotective factor and amyotrophic lateral sclerosis associated angiogenin variants affect neurite extension/pathfinding and survival of motor neurons

Hippocampals neurogenesis is impaired in mice with a deletion in the coiled coil domain of Talpid3—implications for Joubert syndrome

A new role for angiogenin in neurite growth and pathfinding: implications for amyotrophic lateral sclerosis

Adaptive Capacity of a DNA Polymerase Clamp-loader ATPase Complex

Lack of exacerbation of neurodegeneration in a double transgenic mouse model of mutant LRRK2 and tau

Recapitulating Evolutionary Divergence in a Single Cis-Regulatory Element Is Sufficient to Cause Expression Changes of the Lens Gene Tdrd7

Higher intensity of purifying selection on >90% of the human genes revealed by the intrinsic replacement mutation rates

Prevalence of the F-type lectin domain

Patterns of transitional mutation biases within and among mammalian genomes

Role of Na(v)1.9 in activity-dependent axon growth in motoneurons

Thermodynamic binding studies of bivalent oligosaccharides to galectin-1, galectin-3, and the carbohydrate recognition domain of galectin-3

Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies

Signatures of ecological resource availability in the animal and plant proteomes

Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6

Peanut lectin stimulates proliferation of colon cancer cells by interaction with glycosylated CD44v6 isoforms and consequential activation of c-Met and MAPK: functional implications for disease-associated glycosylation changes

Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6

Linkage analysis conditional on HLA status in a large north american pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12

Single cell analysis demonstrating somatic mosaicism involving 11p in a patient with paternal isodisomy and Beckwith—Wiedemann syndrome

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