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Comparison of X-chromosome inactivation patterns in multiple tissues from human females

Journal of medical genetics, 2008-05, Vol.45 (5), p.309-313

2008

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Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

Journal of medical genetics, 2006-05, Vol.43 (5), p.e21-e21

2006

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Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome

International Journal of Obesity, 2009-02, Vol.33 (2), p.273-283

2009

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Circulating adiponectin levels, body composition and obesity-related variables in Prader-Willi syndrome: comparison with obese subjects

International Journal of Obesity, 2006-02, Vol.30 (2), p.382-387

2006

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Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

Journal of medical genetics, 2003-08, Vol.40 (8), p.568-574

2003

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Brief Report: Non-Random X Chromosome Inactivation in Females with Autism

Journal of autism and developmental disorders, 2005-10, Vol.35 (5), p.675-681

2005

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Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH

Cytogenetic and genome research, 2009-01, Vol.124 (2), p.113-120

2009

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Joint Lubricants As Delivery Methods For Multipotent Stromal Cells

Osteoarthritis and cartilage, 2023-03, Vol.31, p.S220-S221

2023

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Zinc and Cadmium Can Promote Rapid Nuclear Translocation of Metal Response Element-binding Transcription Factor-1

The Journal of biological chemistry, 2000-03, Vol.275 (13), p.9377-9384

2000

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Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array

American journal of medical genetics. Part A, 2008-09, Vol.146A (18), p.2346-2354

2008

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Practice parameter: evaluation of the child with microcephaly (an evidence-based review): report of the quality standards subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society

Neurology, 2010-03, Vol.74 (13), p.1080-1081

2010

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Reversible activation of mouse metal response element-binding transcription factor 1 DNA binding involves zinc interaction with the zinc finger domain

Molecular and Cellular Biology, 1997-05, Vol.17 (5), p.2781-2789

1997

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Functional Heterogeneity in the Zinc Fingers of Metalloregulatory Protein Metal Response Element-binding Transcription Factor-1

The Journal of biological chemistry, 2000-11, Vol.275 (47), p.37194-37201

2000

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No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)

Journal of medical genetics, 2002-11, Vol.39 (11), p.e70-70

2002

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Participation of upstream stimulator factor (USF) in cadmium-induction of the mouse metallothionein-I gene

Nucleic acids research, 1998-11, Vol.26 (22), p.5182-5189

1998

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Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD

Genomics (San Diego, Calif.), 2005, Vol.85 (1), p.85-91

2005

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Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region

Journal of medical genetics, 2002-03, Vol.39 (3), p.202-204

2002

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Validation of the Agilent 244K Oligonucleotide Array- Based Comparative Genomic Hybridization Platform for Clinical Cytogenetic Diagnosis

American journal of clinical pathology, 2009-09, Vol.132 (3), p.349-360

2009

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Single-amino acid substitutions eliminate lysine inhibition of maize dihydrodipicolinate synthase

Proceedings of the National Academy of Sciences - PNAS, 1996-03, Vol.93 (5), p.1962-1966

1996

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Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

Pediatrics (Evanston), 2004-03, Vol.113 (3 Pt 1), p.565-573

2004

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Whole genome microarray analysis of gene expression in subjects with fragile X syndrome

Genetics in medicine, 2007-07, Vol.9 (7), p.464-472

2007

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Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities

Genetic testing, 2007-12, Vol.11 (4), p.467-476

2007

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Lysine accumulation in maize cell cultures transformed with a lysine-insensitive form of maize dihydrodipicolinate synthase

Theoretical and applied genetics, 1996, Vol.92 (1), p.70-77

1996

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Surface roughness and the scattering of glancing-angle x rays : application to x-ray lenses

Journal of applied physics, 1993-07, Vol.74 (2), p.877-883

1993

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The DNA Binding Activity of Metal Response Element-binding Transcription Factor-1 Is Activated in Vivo and in Vitro by Zinc, but Not by Other Transition Metals

The Journal of biological chemistry, 1998-03, Vol.273 (12), p.7127-7133

1998

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Comparison of X-chromosome inactivation patterns in multiple tissues from human females

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

Genetic subtype differences in neural circuitry of food motivation in Prader-Willi syndrome

Circulating adiponectin levels, body composition and obesity-related variables in Prader-Willi syndrome: comparison with obese subjects

Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

Brief Report: Non-Random X Chromosome Inactivation in Females with Autism

Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH

Joint Lubricants As Delivery Methods For Multipotent Stromal Cells

Zinc and Cadmium Can Promote Rapid Nuclear Translocation of Metal Response Element-binding Transcription Factor-1

Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array

Practice parameter: evaluation of the child with microcephaly (an evidence-based review): report of the quality standards subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society

Reversible activation of mouse metal response element-binding transcription factor 1 DNA binding involves zinc interaction with the zinc finger domain

Functional Heterogeneity in the Zinc Fingers of Metalloregulatory Protein Metal Response Element-binding Transcription Factor-1

No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)

Participation of upstream stimulator factor (USF) in cadmium-induction of the mouse metallothionein-I gene

Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD

Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region

Validation of the Agilent 244K Oligonucleotide Array- Based Comparative Genomic Hybridization Platform for Clinical Cytogenetic Diagnosis

Single-amino acid substitutions eliminate lysine inhibition of maize dihydrodipicolinate synthase

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

Whole genome microarray analysis of gene expression in subjects with fragile X syndrome

Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities

Lysine accumulation in maize cell cultures transformed with a lysine-insensitive form of maize dihydrodipicolinate synthase

Surface roughness and the scattering of glancing-angle x rays : application to x-ray lenses

The DNA Binding Activity of Metal Response Element-binding Transcription Factor-1 Is Activated in Vivo and in Vitro by Zinc, but Not by Other Transition Metals

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