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Recovering 3D human pose from monocular images

IEEE transactions on pattern analysis and machine intelligence, 2006-01, Vol.28 (1), p.44-58

2006

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Histograms of oriented gradients for human detection

2005 IEEE Computer Society Conference on Computer Vision and Pattern Recognition (CVPR'05), 2005, Vol.1, p.886-893 vol. 1

2005

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Hierarchical part-based visual object categorization

2005 IEEE Computer Society Conference on Computer Vision and Pattern Recognition (CVPR'05), 2005, Vol.1, p.710-715 vol. 1

2005

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Genotyping an immunodeficiency causing c.1624-11G>A ZAP70 mutation in Canadian Mennonites

BMC medical genetics, 2016-07, Vol.17 (1), p.50-50, Article 50

2016

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Molecular basis of succinylcholine sensitivity in a prairie Hutterite kindred and genetic characterization of the region containing the BCHE gene

Molecular genetics and metabolism, 2007-02, Vol.90 (2), p.210-216

2007

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Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs disease

American journal of human genetics, 1991-11, Vol.49 (5), p.1041-1054

1991

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Characterization of the murine hyaluronidase gene region reveals complex organization and cotranscription of Hyal1 with downstream genes, Fus2 and Hyal3

The Journal of biological chemistry, 2002-06, Vol.277 (25), p.23008-23018

2002

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Structural and Functional Characterization of Streptomyces plicatus β-N-Acetylhexosaminidase by Comparative Molecular Modeling and Site-directed Mutagenesis

The Journal of biological chemistry, 1998-07, Vol.273 (31), p.19618-19624

1998

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Mutations in HYAL1, a Member of a Tandemly Distributed Multigene Family Encoding Disparate Hyaluronidase Activities, Cause a Newly Described Lysosomal Disorder, Mucopolysaccharidosis IX

Proceedings of the National Academy of Sciences - PNAS, 1999-05, Vol.96 (11), p.6296-6300

1999

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Human growth factor receptor bound 14 binds the activated insulin receptor and alters the insulin-stimulated tyrosine phosphorylation levels of multiple proteins

Biochemistry and cell biology, 2001, Vol.79 (1), p.21-32

2001

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A mutation common in non-jewish Tay-Sachs disease: Frequency and RNA studies

Human mutation, 1992, Vol.1 (4), p.303-309

1992

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A novel HEXA mutation [1393G>A (D465N)] in a Mexican Tay-Sachs disease patient

Human mutation, 2001-05, Vol.17 (5), p.437-437

2001

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A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening

American journal of human genetics, 1992-10, Vol.51 (4), p.793-801

1992

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Assignment of Growth Factor Receptor-Bound Protein 10 (GRB10) to Human Chromosome 7p11.2–p12

Genomics (San Diego, Calif.), 1997-02, Vol.40 (1), p.215-216

1997

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A second mutation associated with apparent β-hexosaminidase A pseudodeficiency : identification and frequency estimation

American journal of human genetics, 1993-12, Vol.53 (6), p.1198-1205

1993

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Screening for Carriers of Tay-Sachs Disease among Ashkenazi Jews: A Comparison of DNA-Based and Enzyme-Based Tests

The New England journal of medicine, 1990-07, Vol.323 (1), p.6-12

1990

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Diagnostic heteroduplexes: simple detection of carriers of a 4-bp insertion mutation in Tay-Sachs disease

American journal of human genetics, 1990-01, Vol.46 (1), p.183-184

1990

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3D human pose from silhouettes by relevance vector regression

Proceedings of the 2004 IEEE Computer Society Conference on Computer Vision and Pattern Recognition, 2004. CVPR 2004, 2004, Vol.2, p.II-II

2004

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Kinematic jump processes for monocular 3D human tracking

2003 IEEE Computer Society Conference on Computer Vision and Pattern Recognition, 2003. Proceedings, 2003, Vol.1, p.I-I

2003

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Covariance scaled sampling for monocular 3D body tracking

Proceedings of the 2001 IEEE Computer Society Conference on Computer Vision and Pattern Recognition. CVPR 2001, 2001, Vol.1, p.I-I

2001

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Benign HEXA mutations, C739T(R247W) and C745T(R249W), cause beta-hexosaminidase A pseudodeficiency by reducing the alpha-subunit protein levels

The Journal of biological chemistry, 1997-06, Vol.272 (23), p.14975-14982

1997

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A locus for Bowen-Conradi syndrome maps to chromosome region 12p13.3

American journal of medical genetics, 2005-01, Vol.132A (2), p.136-143

2005

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A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I

Human molecular genetics, 1995-03, Vol.4 (3), p.493-495

1995

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W474C amino acid substitution affects early processing of the alpha-subunit of beta-hexosaminidase A and is associated with subacute G(M2) gangliosidosis

Human mutation, 1998, Vol.11 (6), p.432-442

1998

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Naturally occurring mutations in GM2 gangliosidosis: a compendium

Advances in genetics, 2001, Vol.44, p.199-224

2001

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Recovering 3D human pose from monocular images

Histograms of oriented gradients for human detection

Hierarchical part-based visual object categorization

Genotyping an immunodeficiency causing c.1624-11G>A ZAP70 mutation in Canadian Mennonites

Molecular basis of succinylcholine sensitivity in a prairie Hutterite kindred and genetic characterization of the region containing the BCHE gene

Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs disease

Characterization of the murine hyaluronidase gene region reveals complex organization and cotranscription of Hyal1 with downstream genes, Fus2 and Hyal3

Structural and Functional Characterization of Streptomyces plicatus β-N-Acetylhexosaminidase by Comparative Molecular Modeling and Site-directed Mutagenesis

Mutations in HYAL1, a Member of a Tandemly Distributed Multigene Family Encoding Disparate Hyaluronidase Activities, Cause a Newly Described Lysosomal Disorder, Mucopolysaccharidosis IX

Human growth factor receptor bound 14 binds the activated insulin receptor and alters the insulin-stimulated tyrosine phosphorylation levels of multiple proteins

A mutation common in non-jewish Tay-Sachs disease: Frequency and RNA studies

A novel HEXA mutation [1393G>A (D465N)] in a Mexican Tay-Sachs disease patient

A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening

Assignment of Growth Factor Receptor-Bound Protein 10 (GRB10) to Human Chromosome 7p11.2–p12

A second mutation associated with apparent β-hexosaminidase A pseudodeficiency : identification and frequency estimation

Screening for Carriers of Tay-Sachs Disease among Ashkenazi Jews: A Comparison of DNA-Based and Enzyme-Based Tests

Diagnostic heteroduplexes: simple detection of carriers of a 4-bp insertion mutation in Tay-Sachs disease

3D human pose from silhouettes by relevance vector regression

Kinematic jump processes for monocular 3D human tracking

Covariance scaled sampling for monocular 3D body tracking

Benign HEXA mutations, C739T(R247W) and C745T(R249W), cause beta-hexosaminidase A pseudodeficiency by reducing the alpha-subunit protein levels

A locus for Bowen-Conradi syndrome maps to chromosome region 12p13.3

A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I

W474C amino acid substitution affects early processing of the alpha-subunit of beta-hexosaminidase A and is associated with subacute G(M2) gangliosidosis

Naturally occurring mutations in GM2 gangliosidosis: a compendium

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