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Defects in tRNA Anticodon Loop 2′-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1

Human mutation, 2015-12, Vol.36 (12), p.1176-1187

2015

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Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

Cell, 1997-02, Vol.88 (3), p.367-374

1997

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O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling

The Journal of biological chemistry, 2018-07, Vol.293 (27), p.10810-10824

2018

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Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder

Molecular psychiatry, 2019-11, Vol.24 (11), p.1748-1768

2019

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A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A

Journal of medical genetics, 2015-04, Vol.52 (4), p.269-274

2015

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Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations

European journal of human genetics : EJHG, 2012-07, Vol.20 (7), p.806-809

2012

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A non-coding variant in the 5' UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability

European journal of human genetics : EJHG, 2016-11, Vol.24 (11), p.1612-1616

2016

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Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia

Science advances, 2023-05, Vol.9 (18), p.eade2044-eade2044

2023

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Defects in tRNA anticodon loop 2'-O-methylation are implicated in non-syndromic X-linked intellectual disability due to mutations in FTSJ1

Human mutation, 2015-09, Vol.36 (12), p.1176-1187

2015

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Common chromosomal fragile site FRA16D sequence : identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Human molecular genetics, 2000-07, Vol.9 (11), p.1651-1663

2000

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Common chromosomal fragile site FRA16D mutation in cancer cells

Human molecular genetics, 2005-05, Vol.14 (10), p.1341-1349

2005

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Chromosomal fragile site FRA16D and DNA instability in cancer

Cancer research (Chicago, Ill.), 2000-03, Vol.60 (6), p.1683-1689

2000

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FRA10B Structure Reveals Common Elements in Repeat Expansion and Chromosomal Fragile Site Genesis

Molecular cell, 1998-05, Vol.1 (6), p.773-781

1998

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Guided Participation and Parental Tutoring in Preschool Children with Autism: A Pilot Study of Relationship Development Intervention (RDI)

Psychoanalytic inquiry, 2023-04, Vol.43 (3), p.184-198

2023

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Late Iron Age and Medieval Remains North of Front Street, Dinnington, Newcastle Upon Tyne

Archaeologia Aeliana, 2023-01, Vol.52, p.235

2023

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Restoration and the Affective Ecologies of Healing: Buffalo and the Fort Peck Tribes

Conservation and society, 2018-01, Vol.16 (1), p.21-29

2018

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Voiding difficulties in the elderly

Post Reproductive Health, 2014-12, Vol.20 (4), p.143-147

2014

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Wives and warriors: The royal women of Dahomey as representatives of the kingdom

The Routledge Companion to Black Women’s Cultural Histories, 2021, Vol.1, p.225-235

Larsen, Lynne Ellsworth

1, 2021

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Violence Prevention after Columbine: A Survey of High School Mental Health Professionals

Children & schools, 2005-07, Vol.27 (3), p.157-165

2005

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Hobson, J Allan. The Dreaming Brain // Review

Psychology Today, 1988, Vol.22 (10), p.71

1988

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Little museums: over 1,000 small (and not-so-small) American showplaces

Curator, 1998, Vol.41 (2), p.140-141

1998

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Defects in tRNA Anticodon Loop 2′-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1

Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder

A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A

Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations

A non-coding variant in the 5' UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability

Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia

Defects in tRNA anticodon loop 2'-O-methylation are implicated in non-syndromic X-linked intellectual disability due to mutations in FTSJ1

Common chromosomal fragile site FRA16D sequence : identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

Common chromosomal fragile site FRA16D mutation in cancer cells

Chromosomal fragile site FRA16D and DNA instability in cancer

FRA10B Structure Reveals Common Elements in Repeat Expansion and Chromosomal Fragile Site Genesis

Guided Participation and Parental Tutoring in Preschool Children with Autism: A Pilot Study of Relationship Development Intervention (RDI)

Late Iron Age and Medieval Remains North of Front Street, Dinnington, Newcastle Upon Tyne

Restoration and the Affective Ecologies of Healing: Buffalo and the Fort Peck Tribes

Voiding difficulties in the elderly

Wives and warriors: The royal women of Dahomey as representatives of the kingdom

Violence Prevention after Columbine: A Survey of High School Mental Health Professionals

Hobson, J Allan. The Dreaming Brain // Review

Little museums: over 1,000 small (and not-so-small) American showplaces

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