S. Dryja: search on Z-Library

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51

BDDC methods for discontinuous Galerkin discretization of elliptic problems

Maksymilian Dryja, Juan Galvis, Marcus Sarkis

Journal:

Journal of Complexity

Year:

2007

Language:

english

File:

PDF, 309 KB

english, 2007

52

10.1038/10305

Pierce, Eric A., Quinn, Tracey, Meehan, Terrence, McGee, Terri L., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 632 KB

english, 1999

53

Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma

Godbout, R., Dryja, T. P., Squire, J., Gallie, B. L., Phillips, R. A.

Journal:

Year:

1983

File:

PDF, 667 KB

1983

54

Parental origin of mutations of the retinoblastoma gene

Dryja, Thaddeus P., Mukai, Shizuo, Petersen, Robert, Rapaport, Joyce M., Walton, David, Yandell, David W.

Journal:

Year:

1989

File:

PDF, 389 KB

1989

55

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

Dryja, Thaddeus P., McGee, Terri L., Reichel, Elias, Hahn, Lauri B., Cowley, Glenn S., Yandell, David W., Sandberg, Michael A., Berson, Eliot L.

Journal:

Year:

1990

File:

PDF, 384 KB

1990

56

Deficiencies in sight with the candidate gene approach

Dryja, Thaddeus P.

Journal:

Year:

1990

File:

PDF, 154 KB

1990

57

Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene

Sakai, Toshiyuki, Ohtani, Naoko, McGee, Terri L., Robbins, Paul D., Dryja, Thaddeus P.

Journal:

Year:

1991

File:

PDF, 808 KB

1991

58

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

Kajiwara, Kazuto, Hahn, Lauri B., Mukai, Shizuo, Travis, Gabriel H., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Year:

1991

File:

PDF, 561 KB

1991

59

10.1038/70499

Morimura, Hiroyuki, Saindelle-Ribeaudeau, Florence, Berson, Eliot L, Dryja, Thaddeus P

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 135 KB

english, 1999

60

10.1038/70496

Morimura, Hiroyuki, Saindelle-Ribeaudeau, Florence, Berson, Eliot L, Dryja, Thaddeus P

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 291 KB

english, 1999

61

10.1038/9707

Dryja, Thaddeus P., Yamamoto, Hiroyuki, Simon, András, Eriksson, Ulf, Harris, Eddie, Berson, Eliot L.

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 280 KB

english, 1999

62

Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation

Nishiguchi, Koji M., Sandberg, Michael A., Kooijman, Aart C., Martemyanov, Kirill A., Pott, Jan W. R., Hagstrom, Stephanie A., Arshavsky, Vadim Y., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Year:

2004

Language:

english

File:

PDF, 277 KB

english, 2004

63

Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle

Hartong, Dyonne T, Dange, Mayura, McGee, Terri L, Berson, Eliot L, Dryja, Thaddeus P, Colman, Roberta F

Journal:

Nature Genetics

Year:

2008

Language:

english

File:

PDF, 308 KB

english, 2008

64

Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness

Yamamoto, Shuji, Sippel, Kimberly C., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 593 KB

1997

65

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with Retinitis pigmentosa

North, Michael A., Nishina, Patsy M., Berson, Eliot L., Dryja, Thaddeus P., Hagstrom, Stephanie A.

Journal:

Nature Genetics

Year:

1998

File:

PDF, 369 KB

1998

66

A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens

Kajiwara, Kazuto, Sandberg, Michael A., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 590 KB

1993

67

A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

Rosenfeld, Philip J., Cowley, Glenn S., McGee, Terri L., Sandberg, Michael A., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1992

File:

PDF, 573 KB

1992

68

Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa

McLaughlin, Margaret E., Sandberg, Michael A., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 579 KB

1993

69

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

Dryja, Thaddeus P., Berson, Eliot L., Rao, Vikram R., Oprian, Daniel D.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 367 KB

1993

70

Missense mutation in the gene encoding the α subunit of rod transducin in the Nougaret form of congenital stationary night blindness

Dryja, Thaddeus P., Hahn, Lauri B., Reboul, Thierry, Arnaud, Bernard

Journal:

Nature Genetics

Year:

1996

File:

PDF, 342 KB

1996

71

Autosomal recessive retinitis pigmentosa caused by mutations in the α subunit of rod cGMP phosphodiesterase

Huang, Sherleen H., Pittler, Steven J., Huang, Xizhong, Oliveira, Luanne, Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 489 KB

1995

72

Concordance of Bacterial Cultures with Endotoxin and Interleukin-6 in Necrotizing Enterocolitis

Linda C. Duffy, Maria A. Zielezny, Vivien Carrion, Elizabeth Griffiths, Diane Dryja, Milo Hilty, Christopher Rook, Frederick Morin

Journal:

Digestive Diseases and Sciences

Year:

1997

Language:

english

File:

PDF, 135 KB

english, 1997

73

A Dirichlet-Neumann Algorithm for Mortar Saddle Point Problems

Maksymilian Dryja

Journal:

BIT Numerical Mathematics

Year:

2002

Language:

english

File:

PDF, 181 KB

english, 2002

74

Effects of AIN457, a Fully Human Antibody to Interleukin-17A, on Psoriasis, Rheumatoid Arthritis, and Uveitis

Hueber, W., Patel, D. D., Dryja, T., Wright, A. M., Koroleva, I., Bruin, G., Antoni, C., Draelos, Z., Gold, M. H., Durez, P.

Journal:

Science Translational Medicine

Year:

2010

Language:

english

File:

PDF, 997 KB

english, 2010

75

Neumann-Neumann methods for a DG discretization on geometrically nonconforming substructures

Maksymilian Dryja, Juan Galvis, Marcus Sarkis

Journal:

Numerical Methods for Partial Differential Equations

Year:

2012

Language:

english

File:

PDF, 351 KB

english, 2012

76

Somatic mutations at a heterozygous autosomal locus in human cells occur more frequently by allele loss than by intragenic structural alterations

D. W. Yandell, T. P. Dryja, J. B. Little

Journal:

Somatic Cell and Molecular Genetics

Year:

1986

Language:

english

File:

PDF, 984 KB

english, 1986

77

Reduction of virus shedding byB. bifidumin experimentally induced MRV infection

L. C. Duffy, M. A. Zielezny, M. Riepenhoff-Talty, D. Dryja, S. Sayahtaheri-Altaie, E. Griffiths, D. Ruffin, H. Barrett, P. L. Ogra

Journal:

Digestive Diseases and Sciences

Year:

1994

Language:

english

File:

PDF, 744 KB

english, 1994

78

Molecular genetic analysis of recessive mutations at a heterozygous autosomal locus in human cells

D.W Yandell, T.P Dryja, J.B Little

Journal:

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Year:

1990

Language:

english

File:

PDF, 1.39 MB

english, 1990

79

Clinical and Molecular Characteristics of Staphylococcal Skin Abscesses in Children

Howard Faden, Rebecca Rose, Alan Lesse, Celeste Hollands, Diane Dryja, Philip L. Glick

Journal:

The Journal of Pediatrics

Year:

2007

Language:

english

File:

PDF, 321 KB

english, 2007

80

Hypermethylation in the retinoblastoma gene is associated with unilateral, sporadic retinoblastoma

Naoko Ohtani-Fujita, Thaddeus P Dryja, Joyce M Rapaport, Tsuyoshi Fujita, Satoshi Matsumura, Kotaro Ozasa, Yoshiyuki Watanabe, Kyohei Hayashi, Koshi Maeda, Shigeru Kinoshita, Takafumi Matsumura, Yoshi

Journal:

Cancer Genetics and Cytogenetics

Year:

1997

Language:

english

File:

PDF, 645 KB

english, 1997

81

Evaluation of the Rhodopsin Kinase Gene in Patients with Retinitis Pigmentosa

SHUJI YAMAMOTO, SHAHROKH C KHANI, ELIOT L BERSON, THADDEUS P DRYJA

Journal:

Experimental Eye Research

Year:

1997

Language:

english

File:

PDF, 243 KB

english, 1997

82

Evaluation of the Myosin VIIA Gene and Visual Function in Patients with Usher Syndrome Type I

Amitabh K Bharadwaj, Joseph P Kasztejna, Syed Huq, Eliot L Berson, Thaddeus P Dryja

Journal:

Experimental Eye Research

Year:

2000

Language:

english

File:

PDF, 152 KB

english, 2000

83

Complete Genomic Sequence of the Human Retinoblastoma Susceptibility Gene

Junya Toguchida, Terri L. McGee, Jennifer C. Paterson, Janine R. Eagle, Stephanie Tucker, David W. Yandell, Thaddeus P. Dryja

Journal:

Year:

1993

File:

PDF, 541 KB

1993

84

Further Screening of the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa

Rajani Vaithinathan, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Year:

1994

File:

PDF, 158 KB

1994

85

Nonallelic Heterogeneity in Autosomal Dominant Retinitis Pigmentosa with Incomplete Penetrance

Stella K. Kim, Jonathan L. Haines, Eliot L. Betson, Thaddeus P. Dryja

Journal:

Year:

1994

File:

PDF, 73 KB

1994

86

Characterization and Chromosomal Localization of the Gene for Human Rhodopsin Kinase

Shahrokh C. Khani, Marc Abitbol, Shuji Yamamoto, Ivana Maravic-Magovcevic, Thaddeus P. Dryja

Journal:

Year:

1996

Language:

english

File:

PDF, 204 KB

english, 1996

87

Presence of cysteinyldopa in the mature bovine eye

Thaddeus P. Dryja, Daniel M. Albert, Ewald Rosengren, Ted W. Reid

Journal:

Experimental Eye Research

Year:

1977

Language:

english

File:

PDF, 462 KB

english, 1977

88

Glial cell component in retinoblastoma

Joseph L. Craft, Delia N. Sang, Thaddeus P. Dryja, Robert J. Brockhurst, Nancy L. Robinson, Daniel M. Albert

Journal:

Experimental Eye Research

Year:

1985

Language:

english

File:

PDF, 21.22 MB

english, 1985

89

Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNA

Paul R. Cotran, Peter J. Ringens, John W. Crabb, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Experimental Eye Research

Year:

1990

Language:

english

File:

PDF, 539 KB

english, 1990

90

Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase

Paul R. Cotran, Gail A.P. Bruns, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Experimental Eye Research

Year:

1991

Language:

english

File:

PDF, 1.43 MB

english, 1991

91

Mapping of the human cone transducin α-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease

Ivana Magovcevic, Stanislawa Weremowicz, Cynthia C. Morton, Shao-Ling Fong, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Year:

1995

Language:

english

File:

PDF, 304 KB

english, 1995

92

Alleles in the HtrA Serine Peptidase 1 Gene Alter the Risk of Neovascular Age-Related Macular Degeneration

Margaret M. DeAngelis, Fei Ji, Scott Adams, Margaux A. Morrison, Amanda J. Harring, Meredith O. Sweeney, Antonio Capone Jr, Joan W. Miller, Thaddeus P. Dryja, Jurg Ott, Ivana K. Kim

Journal:

Year:

2008

Language:

english

File:

PDF, 396 KB

english, 2008

93

Retinal histopathology of an autopsy eye with advanced retinitis pigmentosa in a family with rhodopsin Glu181Lys

King To, Michael Adamian, Thaddeus P Dryja, Eliot L Berson

Journal:

American Journal of Ophthalmology

Year:

2000

Language:

english

File:

PDF, 435 KB

english, 2000

94

Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture

Thaddeus P Dryja

Journal:

American Journal of Ophthalmology

Year:

2000

Language:

english

File:

PDF, 1.49 MB

english, 2000

95

Two families from New England with usher syndrome type IC with distinct haplotypes

Margaret M DeAngelis, Terri L McGee, Bronya J.B Keats, Rima Slim, Eliot L Berson, Thaddeus P Dryja

Journal:

American Journal of Ophthalmology

Year:

2001

Language:

english

File:

PDF, 250 KB

english, 2001

96

Histopathologic study of variation in severity of retinitis pigmentosa due to the dominant rhodopsin mutation Pro23His

King To, Michael Adamian, Thaddeus P Dryja, Eliot L Berson

Journal:

American Journal of Ophthalmology

Year:

2002

Language:

english

File:

PDF, 502 KB

english, 2002

97

Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutation

Thomas A. Ciulla, Felipe Tolentino, Jennifer F. Morrow, Thaddeus P. Dryja

Journal:

Survey of Ophthalmology

Year:

1995

Language:

english

File:

PDF, 3.85 MB

english, 1995

98

Intraocular-central nervous system lymphoma: Clinical features, diagnosis, and outcomes

Esen Karamursel Akpek, Irma Ahmed, Frederick H Hochberg, Masoud Soheilian, Thaddeus P Dryja, Frederick A Jakobiec, C.Stephen Foster

Journal:

Year:

1999

Language:

english

File:

PDF, 253 KB

english, 1999

99

Molecular typing of paired bacterial isolates from the adenoid and lateral wall of the nose in children undergoing adenoidectomy: Implications in acute rhinosinusitis

Joel M. Bernstein, Diane Dryja, Timothy F. Murphy

Journal:

Otolaryngology - Head and Neck Surgery

Year:

2001

Language:

english

File:

PDF, 207 KB

english, 2001

100

Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 Allele

T.L. McGee, M. Devoto, J. Ott, E.L. Berson, T.P. Dryja

Journal:

The American Journal of Human Genetics

Year:

1997

Language:

english

File:

PDF, 138 KB

english, 1997

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