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The psychological subtype of intimate partner violence and its effect on mental health: a systematic review with meta-analyses

Systematic reviews, 2022-08, Vol.11 (1), p.163-16, Article 163

2022

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A 20-year experience of 1712 patients with the Biocor porcine bioprosthesis

The Journal of thoracic and cardiovascular surgery, 2009, Vol.137 (1), p.76-81

2009

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Reply to the Editor

The Journal of thoracic and cardiovascular surgery, 2011-02, Vol.141 (2), p.596-597

2011

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Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina

Human molecular genetics, 2005-10, Vol.14 (20), p.3035-3046

2005

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Developmental topographical disorientation and decreased hippocampal functional connectivity

Hippocampus, 2014-11, Vol.24 (11), p.1364-1374

2014

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Channeling Vision: CaV1.4—A Critical Link in Retinal Signal Transmission

BioMed research international, 2018, Vol.2018 (2018), p.1-14

2018

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Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism

Human molecular genetics, 2008-08, Vol.17 (15), p.2405-2415

2008

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Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

Nature genetics, 2000-11, Vol.26 (3), p.319-323

2000

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Familial aggregation in developmental topographical disorientation (DTD)

Cognitive neuropsychology, 2016-11, Vol.33 (7-8), p.388-397

2016

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Evaluation of APOE ɛ2/ɛ3/ɛ4 Alleles in a Cohort of Individuals Affected by Developmental Topographical Disorientation

JAD reports, 2021-07, Vol.5 (1), p.565-570

2021

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Fitness components of Drosophila melanogaster developed on a standard laboratory diet or a typical natural food source

Insect science, 2016-10, Vol.23 (5), p.771-779

2016

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Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A)

Channels (Austin, Tex.), 2018-01, Vol.12 (1), p.17-33

2018

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Congenital stationary night blindness: mutation update and clinical variability

Advances in experimental medicine and biology, 2012, Vol.723, p.371

2012

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Analysis of the human intestinal epithelial cell transcriptional response to Lactobacillus acidophilus, Lactobacillus salivarius, Bifidobacterium lactis and Escherichia coli

Beneficial microbes, 2010-09, Vol.1 (3), p.283-295

2010

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Isolation and characterization of the leucine-rich proteoglycan nyctalopin gene (cNyx) from chick

Mammalian genome, 2005-10, Vol.16 (10), p.815-824

2005

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Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F

Canadian journal of ophthalmology, 2000-06, Vol.35 (4), p.204-213

2000

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Isolation and Characterization of a Calcium Channel Gene, Cacna1f, the Murine Orthologue of the Gene for Incomplete X-Linked Congenital Stationary Night Blindness

Genomics (San Diego, Calif.), 2000-06, Vol.66 (3), p.324-327

2000

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Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness

American journal of human genetics, 1998-04, Vol.62 (4), p.865-875

1998

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Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23

Human genetics, 1998-08, Vol.103 (2), p.124-130

1998

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Transcriptional activity of the human tissue inhibitor of metalloproteinases 1 (TIMP-1) gene in fibroblasts involves elements in the promoter, exon 1 and intron 1

Biochemical journal, 1997-06, Vol.324 ( Pt 2) (2), p.611-617

1997

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Channeling Vision: Ca V 1.4—A Critical Link in Retinal Signal Transmission

BioMed research international, 2018, Vol.2018, p.1-14

2018

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A 2-Megabase Physical Contig Incorporating 43 DNA Markers on the Human X Chromosome at p11.23–p11.22 from ZNF21 to DXS255

Genomics (San Diego, Calif.), 1996-05, Vol.33 (3), p.488-497

1996

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Physical map covering a 2 Mb region in human Xp11.3 distal to DX6849

Gene, 1999-02, Vol.227 (1), p.111-116

1999

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Clustered Organization of Krüppel Zinc-Finger Genes at Xp11.23, Flanking a Translocation Breakpoint at OATL1: A Physical Map with Locus Assignments for ZNF21, ZNF41, ZNF81, and ELK1

Genomics (San Diego, Calif.), 1994-05, Vol.21 (1), p.180-187

1994

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Recent Progress in the Identification of the X-Linked Infantile Spinal Muscular Atrophy ( Xl-SMA ) Gene: Implications for Neuronal Apoptosis

TheScientificWorld, 2001, Vol.1, p.33-33

2001

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The psychological subtype of intimate partner violence and its effect on mental health: a systematic review with meta-analyses

A 20-year experience of 1712 patients with the Biocor porcine bioprosthesis

Reply to the Editor

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina

Developmental topographical disorientation and decreased hippocampal functional connectivity

Channeling Vision: CaV1.4—A Critical Link in Retinal Signal Transmission

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism

Mutations in NYX , encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

Familial aggregation in developmental topographical disorientation (DTD)

Evaluation of APOE ɛ2/ɛ3/ɛ4 Alleles in a Cohort of Individuals Affected by Developmental Topographical Disorientation

Fitness components of Drosophila melanogaster developed on a standard laboratory diet or a typical natural food source

Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A)

Congenital stationary night blindness: mutation update and clinical variability

Analysis of the human intestinal epithelial cell transcriptional response to Lactobacillus acidophilus, Lactobacillus salivarius, Bifidobacterium lactis and Escherichia coli

Isolation and characterization of the leucine-rich proteoglycan nyctalopin gene (cNyx) from chick

Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F

Isolation and Characterization of a Calcium Channel Gene, Cacna1f, the Murine Orthologue of the Gene for Incomplete X-Linked Congenital Stationary Night Blindness

Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness

Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23

Transcriptional activity of the human tissue inhibitor of metalloproteinases 1 (TIMP-1) gene in fibroblasts involves elements in the promoter, exon 1 and intron 1

Channeling Vision: Ca V 1.4—A Critical Link in Retinal Signal Transmission

A 2-Megabase Physical Contig Incorporating 43 DNA Markers on the Human X Chromosome at p11.23–p11.22 from ZNF21 to DXS255

Physical map covering a 2 Mb region in human Xp11.3 distal to DX6849

Clustered Organization of Krüppel Zinc-Finger Genes at Xp11.23, Flanking a Translocation Breakpoint at OATL1: A Physical Map with Locus Assignments for ZNF21, ZNF41, ZNF81, and ELK1

Recent Progress in the Identification of the X-Linked Infantile Spinal Muscular Atrophy ( Xl-SMA ) Gene: Implications for Neuronal Apoptosis

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