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Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia

Nature genetics, 1995-07, Vol.10 (3), p.325-329

1995

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Multiple autism-like behaviors in a novel transgenic mouse model

Behavioural brain research, 2011-03, Vol.218 (1), p.29-41

2011

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A transgenic insertion upstream of Sox9 is associated with dominant XX sex reversal in the mouse

Nature genetics, 2000-12, Vol.26 (4), p.490-494

2000

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

Nature genetics, 2000-01, Vol.24 (1), p.79-83

2000

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A transgenic insertion causing cryptorchidism in mice

Genesis (New York, N.Y. : 2000), 2001-05, Vol.30 (1), p.26-35

2001

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Donor cell leukemia: Report of a case occurring 11 years after allogeneic bone marrow transplantation and review of the literature

American journal of hematology, 2000-01, Vol.63 (1), p.46-53

2000

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Intracorneal positioning of the lens in Pax6-GAL4/VP16 transgenic mice

Molecular vision, 2005-10, Vol.11, p.876-886

2005

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Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport Syndrome

Genomics (San Diego, Calif.), 1999-10, Vol.61 (2), p.113-124

1999

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Malignant peripheral nerve sheath tumor with a t(X;18): A synovial sarcoma variant?

Archives of pathology & laboratory medicine (1976), 2000-06, Vol.124 (6), p.864

2000

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Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3

Mammalian genome, 2002-11, Vol.13 (11), p.625-632

2002

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Smcy transgene does not rescue spermatogenesis in sex-reversed mice

Mammalian genome, 2001-02, Vol.12 (2), p.112-116

2001

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Immunohistochemical determination of HER-2/neu expression in invasive breast carcinoma

American journal of clinical pathology, 2000-05, Vol.113 (5), p.669-674

2000

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Expression of the rat liver carnitine palmitoyltransferase I (CPT-Ialpha) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization

Biochemical journal, 1999-06, Vol.340 ( Pt 2) (2), p.425-432

1999

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Human Glutamate Pyruvate Transaminase (GPT): Localization to 8q24.3, cDNA and Genomic Sequences, and Polymorphic Sites

Genomics (San Diego, Calif.), 1997-03, Vol.40 (2), p.247-252

1997

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Expression of the rat liver carnitine palmitoyltransferase I (CPT-Iα) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization

Biochemical journal, 1999-06, Vol.340 (2), p.425-432

1999

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Malignant peripheral nerve sheath tumor with a t(X;18)

Archives of pathology & laboratory medicine (1976), 2000-06, Vol.124 (6), p.864-867

2000

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Characterization of Human DSPG3, a Small Dermatan Sulfate Proteoglycan

Genomics (San Diego, Calif.), 1996-12, Vol.38 (3), p.399-404

1996

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

American journal of ophthalmology, 2000-06, Vol.129 (6), p.834-835

2000

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Detection of Double Minute Chromosomes in a Child with Acute Lymphoblastic Leukemia

Cancer genetics and cytogenetics, 1998-03, Vol.101 (2), p.138-142

1998

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Multifocal osteosarcoma: an unusual presentation

Journal of pediatric hematology/oncology, 1999-01, Vol.21 (1), p.58-62

1999

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Cytogenetic Analysis of a Scapular Chondromyxoid Fibroma

Cancer genetics and cytogenetics, 1998-07, Vol.104 (1), p.52-56

1998

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Histone posttranslational modifications and cell fate determination: lens induction requires the lysine acetyltransferases CBP and p300

Nucleic acids research, 2013-12, Vol.41 (22), p.10199-10214

2013

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A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis

PloS one, 2012-11, Vol.7 (11), p.e50634-e50634

2012

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Impact of Body Mass Index on Immunogenicity of Pandemic H1N1 Vaccine in Children and Adults

The Journal of infectious diseases, 2014-10, Vol.210 (8), p.1270-1274

2014

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Head Bobber: An Insertional Mutation Causes Inner Ear Defects, Hyperactive Circling, and Deafness

Journal of the Association for Research in Otolaryngology, 2012-06, Vol.13 (3), p.335-349

2012

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Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia

Multiple autism-like behaviors in a novel transgenic mouse model

A transgenic insertion upstream of Sox9 is associated with dominant XX sex reversal in the mouse

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

A transgenic insertion causing cryptorchidism in mice

Donor cell leukemia: Report of a case occurring 11 years after allogeneic bone marrow transplantation and review of the literature

Intracorneal positioning of the lens in Pax6-GAL4/VP16 transgenic mice

Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport Syndrome

Malignant peripheral nerve sheath tumor with a t(X;18): A synovial sarcoma variant?

Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3

Smcy transgene does not rescue spermatogenesis in sex-reversed mice

Immunohistochemical determination of HER-2/neu expression in invasive breast carcinoma

Expression of the rat liver carnitine palmitoyltransferase I (CPT-Ialpha) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization

Human Glutamate Pyruvate Transaminase (GPT): Localization to 8q24.3, cDNA and Genomic Sequences, and Polymorphic Sites

Expression of the rat liver carnitine palmitoyltransferase I (CPT-Iα) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization

Malignant peripheral nerve sheath tumor with a t(X;18)

Characterization of Human DSPG3, a Small Dermatan Sulfate Proteoglycan

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis

Detection of Double Minute Chromosomes in a Child with Acute Lymphoblastic Leukemia

Multifocal osteosarcoma: an unusual presentation

Cytogenetic Analysis of a Scapular Chondromyxoid Fibroma

Histone posttranslational modifications and cell fate determination: lens induction requires the lysine acetyltransferases CBP and p300

A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis

Impact of Body Mass Index on Immunogenicity of Pandemic H1N1 Vaccine in Children and Adults

Head Bobber: An Insertional Mutation Causes Inner Ear Defects, Hyperactive Circling, and Deafness

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