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A marked paucity of granule cells in the developing cerebellum of the Npc1−/− mouse is corrected by a single injection of hydroxypropyl-β-cyclodextrin

Neurobiology of disease, 2014-10, Vol.70, p.117-126

2014

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THE RE-DISCOVERY OF DURAL (MENINGEAL) LYMPHATICS: AMNESIA OR AMBITION?

Lymphology, 2024-06, Vol.56 (3)

Erickson, R.P.

2024

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LYMPHSPIRATION THE IMPORTANCE OF THE STUDY OF DERMATOGLYPHICS FOR LYMPHOLOGISTS

Lymphology, 2022-06, Vol.55 (1)

Erickson, R.P.

2022

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EDITORIAL: CENTRIFUGAL VERSUS CENTRIPETAL ORIGIN(S) OF THE LYMPHATIC SYSTEM: CONTROVERSY (MOSTLY) RESOLVED?

Lymphology, 2023-08, Vol.55 (4)

2023

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Symposium Highlight: BRAIN LYMPHATICS: REDISCOVERY AND NEW INSIGHTS INTO LYMPHATIC INVOLVEMENT IN DISEASES OF HUMAN BRAINS

Lymphology, 2024-10, Vol.57 (1)

2024

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Corrigendum to “Decreased membrane cholesterol in liver mitochondria of the point mutation mouse model of juvenile Niemann-Pick C1, Npc1” [Mitochondrion 51 (2019) 15–21]

Mitochondrion, 2021-11, Vol.61, p.196

2021

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Corrigendum to “Decreased membrane cholesterol in liver mitochondria of the point mutation mouse model of juvenile Niemann-Pick C1, Npc1nmf164” [Mitochondrion 51 (2019) 15–21]

Mitochondrion, 2021-11, Vol.61, p.196-196

2021

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Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery

Lymphology, 2021, Vol.54 (4), p.167

2021

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Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a Sos1 mutation and lack of lymphatic embryonic phenotypes for a homozygous Cx47 mutation in mice

Lymphology, 2022, Vol.55 (3), p.129-134

2022

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Different responses to repeated applications of zingerone in behavioral studies, recordings from intact and cultured TG neurons, and from VR1 receptors

Physiology & behavior, 2000-04, Vol.69 (1), p.177-186

2000

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Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutation

Lymphology, 2021, Vol.54 (2), p.78

2021

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Magnetic phase diagram of ultrathin Fe/Ag(100) films near the reorientation phase transition

Journal of magnetism and magnetic materials, 1997, Vol.165 (1), p.70-73

1997

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Detection of Circular and Linear Transcripts of Sry in Preimplantation Mouse Embryos: Differences in Requirement for Reverse Transcriptase

Biochemical and biophysical research communications, 1994-01, Vol.198 (2), p.492-496

1994

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Towards smaller and faster gas chromatography–mass spectrometry systems for field chemical detection

Journal of Chromatography A, 2005-03, Vol.1067 (1), p.285-294

2005

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Neural responses to bitter compounds in rats

Brain research, 1997-05, Vol.756 (1), p.22-34

1997

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A Case of Agonadism, Skeletal Malformations, Bicuspid Aortic Valve, and Delayed Development with a 16p13.3 Duplication Including GNG13 and SOX8 Upstream Enhancers: Are Either, Both or Neither Involved in the Phenotype?

Molecular syndromology, 2011-01, Vol.1 (4), p.185-191

2011

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Taste of glutamate salts in young and elderly subjects: Role of inosine 5′-monophosphate and ions

Physiology & behavior, 1991-05, Vol.49 (5), p.843-854

1991

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Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy

American journal of human genetics, 1992-10, Vol.51 (4), p.701-708

1992

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Neural mass differences in gustation

Chemical senses, 1985, Vol.10 (4), p.531-548

1985

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Sex Chromosomes evolution: Sharing outside of pairing

Nature (London), 1984-09, Vol.311 (5982), p.106-107

1984

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Altered expression of caveolin-1 and increased cholesterol in detergent insoluble membrane fractions from liver in mice with Niemann–Pick disease type C

Biochimica et biophysica acta, 1997-10, Vol.1361 (3), p.272-280

1997

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N-Ethyl-N-nitrosourea-Induced Null Mutation at the Mouse Car-2 Locus: An Animal Model for Human Carbonic Anhydrase II Deficiency Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1988-03, Vol.85 (6), p.1962-1966

1988

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Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome

Journal of molecular biology, 1985-01, Vol.182 (4), p.477-485

1985

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Sequence Variation in the 5′, Putative Promoter of Sry and Its Possible Relevance to the C57BL/6J-Y-DOM Sex Reversal

Biochemical and biophysical research communications, 1995-03, Vol.208 (2), p.624-628

1995

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Y;16 translocation breakpoint associated with a partial Turner phenotype identifies a foamy virus insertion

Cytogenetic and genome research, 1998-01, Vol.80 (1-4), p.199-203

1998

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A marked paucity of granule cells in the developing cerebellum of the Npc1−/− mouse is corrected by a single injection of hydroxypropyl-β-cyclodextrin

THE RE-DISCOVERY OF DURAL (MENINGEAL) LYMPHATICS: AMNESIA OR AMBITION?

LYMPHSPIRATION THE IMPORTANCE OF THE STUDY OF DERMATOGLYPHICS FOR LYMPHOLOGISTS

EDITORIAL: CENTRIFUGAL VERSUS CENTRIPETAL ORIGIN(S) OF THE LYMPHATIC SYSTEM: CONTROVERSY (MOSTLY) RESOLVED?

Symposium Highlight: BRAIN LYMPHATICS: REDISCOVERY AND NEW INSIGHTS INTO LYMPHATIC INVOLVEMENT IN DISEASES OF HUMAN BRAINS

Corrigendum to “Decreased membrane cholesterol in liver mitochondria of the point mutation mouse model of juvenile Niemann-Pick C1, Npc1” [Mitochondrion 51 (2019) 15–21]

Corrigendum to “Decreased membrane cholesterol in liver mitochondria of the point mutation mouse model of juvenile Niemann-Pick C1, Npc1nmf164” [Mitochondrion 51 (2019) 15–21]

Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discovery

Lack of embryonic homozygous or adult heterozygous lymphatic phenotypes for a Sos1 mutation and lack of lymphatic embryonic phenotypes for a homozygous Cx47 mutation in mice

Different responses to repeated applications of zingerone in behavioral studies, recordings from intact and cultured TG neurons, and from VR1 receptors

Abnormal lymphatic phenotype in a CRISPR mouse model of the human lymphedema-causing Connexin47 R260C point mutation

Magnetic phase diagram of ultrathin Fe/Ag(100) films near the reorientation phase transition

Detection of Circular and Linear Transcripts of Sry in Preimplantation Mouse Embryos: Differences in Requirement for Reverse Transcriptase

Towards smaller and faster gas chromatography–mass spectrometry systems for field chemical detection

Neural responses to bitter compounds in rats

A Case of Agonadism, Skeletal Malformations, Bicuspid Aortic Valve, and Delayed Development with a 16p13.3 Duplication Including GNG13 and SOX8 Upstream Enhancers: Are Either, Both or Neither Involved in the Phenotype?

Taste of glutamate salts in young and elderly subjects: Role of inosine 5′-monophosphate and ions

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy

Neural mass differences in gustation

Sex Chromosomes evolution: Sharing outside of pairing

Altered expression of caveolin-1 and increased cholesterol in detergent insoluble membrane fractions from liver in mice with Niemann–Pick disease type C

N-Ethyl-N-nitrosourea-Induced Null Mutation at the Mouse Car-2 Locus: An Animal Model for Human Carbonic Anhydrase II Deficiency Syndrome

Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome

Sequence Variation in the 5′, Putative Promoter of Sry and Its Possible Relevance to the C57BL/6J-Y-DOM Sex Reversal

Y;16 translocation breakpoint associated with a partial Turner phenotype identifies a foamy virus insertion

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