R. Raha-Chowdhury: search on Z-Library

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1

CAT 53: A protein phosphatase 1 nuclear targeting subunit encoded in the MHC Class I region strongly expressed in regions of the brain involved in memory, learning, and Alzheimer's disease

Ruma Raha-Chowdhury, Simon R. Andrews, Jeffrey R. Gruen

Journal:

Molecular Brain Research

Year:

2005

Language:

english

File:

PDF, 20.13 MB

english, 2005

2

Polymorphisms in the HLA-linked olfactory receptor genes in the Hutterites

Amy C Eklund, Mary Margaret Belchak, Karen Lapidos, Ruma Raha-Chowdhury, Carole Ober

Journal:

Human Immunology

Year:

2000

Language:

english

File:

PDF, 413 KB

english, 2000

3

Alleles at D6S265 and D6S105 define a haemochromatosis-specific genotype

M. Worwood, R. Raha-Chowdhury, M. T. Dorak, C. Darke, D. J. Bowen, A. K. Burnett

Journal:

British Journal of Haematology

Year:

1994

Language:

english

File:

PDF, 428 KB

english, 1994

4

Choroid Plexus Acts as Gatekeeper for TREM2, Abnormal Accumulation of ApoE, and Fibrillary Tau in Alzheimer’s Disease and in Down Syndrome Dementia

Raha-Chowdhury, Ruma, Henderson, James W., Raha, Animesh Alexander, Vuono, Romina, Bickerton, Anastasia, Jones, Elizabeth, Fincham, Robert, Allinson, Kieren, Holland, Anthony, Zaman, Shahid H.

Journal:

Journal of Alzheimer's Disease

Year:

2019

Language:

english

File:

PDF, 1.39 MB

english, 2019

5

Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? : HLA haplotype observations of hemochromatosis from the west coast of Sweden

Karl Sigvard Olsson, Jan Konar, Inge Hoegh Dufva, Anne Ricksten, Ruma Raha-Chowdhury

Journal:

European Journal of Haematology

Year:

2011

Language:

english

File:

PDF, 312 KB

english, 2011

6

New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105

Raha-Chowdhury, Ruma, Bowen, Derrick J., Stone, Caroline, Pointon, Jennifer J., Terwilliger, Joseph D., Shearman, Jeremy D., Robson, Kathryn J.H., Bomford, Adrian, Worwood, Mark

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 549 KB

english, 1995

7

H63D is an haemochromatosis associated allele Reply Reply

FAIRBANKS, V F, BRANDHAGEN, D J, THIBODEAU, S N, SNOW, K, WOLLAN, P C, The UK Haemochromatosis Consortium:,, WORWOOD, M, BOWEN, D J, BURNETT, A K, JACKSON, H A, LAWLESS, S, RAHA-CHOWDHURY, R, SHEARMA

Journal:

Year:

1998

Language:

english

File:

PDF, 175 KB

english, 1998

8

Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis.

Rhodes, D A, Raha-Chowdhury, R, Cox, T M, Trowsdale, J

Journal:

Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 852 KB

english, 1997

9

Contrasting effects of basic fibroblast growth factor and epidermal growth factor on mouse neonatal olfactory mucosa cells

Perrine Barraud, Xiaoling He, Chao Zhao, Chrystelle Ibanez, Ruma Raha-Chowdhury, Maeve A. Caldwell, Robin J. M. Franklin

Journal:

European Journal of Neuroscience

Year:

2007

Language:

english

File:

PDF, 1.60 MB

english, 2007

10

A new highly polymorphic marker in the 5' untranslated region of HLA-F shows strong allelic association with haemochromatosis

R. Raha-Chowdhury,D. J. Bowen,M. Worwood

Journal:

Year:

1996

Language:

english

File:

PDF, 451 KB

english, 1996

11

Disrupted iron regulation in the brain and periphery in cocaine addiction

Ersche, K D, Acosta-Cabronero, J, Jones, P S, Ziauddeen, H, van Swelm, R P L, Laarakkers, C M M, Raha-Chowdhury, R, Williams, G B

Journal:

Translational Psychiatry

Year:

2017

Language:

english

File:

PDF, 1.38 MB

english, 2017

12

Astrocytes and oligodendrocytes can be generated from NG2+ progenitors after acute brain injury: intracellular localization of oligodendrocyte transcription factor 2 is associated with their fate choice

Jing-Wei Zhao, Ruma Raha-Chowdhury, James W. Fawcett, Colin Watts

Journal:

European Journal of Neuroscience

Year:

2009

Language:

english

File:

PDF, 1.78 MB

english, 2009

13

HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overload

K. Sigvard Olsson, Bernd Ritter, Ruma Raha-Chowdhury

Journal:

European Journal of Haematology

Year:

2010

Language:

english

File:

PDF, 404 KB

english, 2010

14

Neuroprotective Effect of TREM-2 in Aging and Alzheimer’s Disease Model

Raha, Animesh Alexander, Henderson, James W., Stott, Simon R.W., Vuono, Romina, Foscarin, Simona, Friedland, Robert P., Zaman, Shahid H., Raha-Chowdhury, Ruma

Journal:

Journal of Alzheimer's Disease

Year:

2016

Language:

english

File:

PDF, 7.27 MB

english, 2016

15

Liver iron concentrations in sudden infant death syndrome.

Moore, C A, Raha-Chowdhury, R, Fagan, D G, Worwood, M

Journal:

Archives of Disease in Childhood

Year:

1994

Language:

english

File:

PDF, 726 KB

english, 1994

16

Blood ferritin concentrations in newborn infants and the sudden infant death syndrome.

Raha-Chowdhury, R, Moore, C A, Bradley, D, Henley, R, Worwood, M

Journal:

Journal of Clinical Pathology

Year:

1996

Language:

english

File:

PDF, 592 KB

english, 1996

17

Distribution of alleles at D6S105 and D6S265 with possible HLA haplotype associations

M. Worwood, R. Raha-Chowdhury, C. Darke

Journal:

Tissue Antigens

Year:

1994

Language:

english

File:

PDF, 261 KB

english, 1994

18

Erythromyeloid-Derived TREM2: A Major Determinant of Alzheimer’s Disease Pathology in Down Syndrome

Raha-Chowdhury, Ruma, Henderson, James W., Raha, Animesh Alexander, Stott, Simon R.W., Vuono, Romina, Foscarin, Simona, Wilson, Liam, Annus, Tiina, Fincham, Robert, Allinson, Kieren, Devalia, Vinod, F

Journal:

Journal of Alzheimer's Disease

Year:

2017

Language:

english

File:

PDF, 1.48 MB

english, 2017

19

Haemochromatosis: a gene at last?

Robson, K J, Shearman, J D, Merryweather-Clarke, A T, Pointon, J J, Rosenberg, W M, Walker, A P, Dooley, J S, Bomford, A, Raha-Chowdhury, R, Worwood, M

Journal:

Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 703 KB

english, 1997

20

Transplantation of Neural Precursors Derived from Induced Pluripotent Cells Preserve Perineuronal Nets and Stimulate Neural Plasticity in ALS Rats

Forostyak, Serhiy, Forostyak, Oksana, Kwok, Jessica C. F., Romanyuk, Nataliya, Rehorova, Monika, Kriska, Jan, Dayanithi, Govindan, Raha-Chowdhury, Ruma, Jendelova, Pavla, Anderova, Miroslava, Fawcett,

Journal:

International Journal of Molecular Sciences

Year:

2020

File:

PDF, 4.50 MB

2020

21

Postmortem blood ferritin concentrations in sudden infant death syndrome.

Worwood, M, Raha-Chowdhury, R, Fagan, D G, Moore, C A

Journal:

Journal of Clinical Pathology

Year:

1995

Language:

english

File:

PDF, 851 KB

english, 1995

22

Human gamma-aminobutyric acid B receptor gene: complementary DNA cloning, expression, chromosomal location, and genomic organization

Vita L Goei, Jenny Choi, Jung Ahn, Christopher L Bowlus, Ruma Raha-Chowdhury, Jeffrey R Gruen

Journal:

Biological Psychiatry

Year:

1998

Language:

english

File:

PDF, 215 KB

english, 1998

23

Red cell destruction by human monocytes — changes in intracellular ferritin concentration and phenotype

R. Raha-Chowdhury, B. J. Williams, M. Worwood

Journal:

European Journal of Haematology

Year:

1993

Language:

english

File:

PDF, 538 KB

english, 1993

24

Letter to the editor

Sigvard Olsson, Ruma Raha-Chowdhury

Journal:

European Journal of Haematology

Year:

2012

Language:

english

File:

PDF, 82 KB

english, 2012

25

Expression and cellular localization of hepcidin mRNA and protein in normal rat brain

Raha-Chowdhury, Ruma, Raha, Animesh Alexander, Forostyak, Serhiy, Zhao, Jing-Wei, Stott, Simon Russell William, Bomford, Adrian

Journal:

BMC Neuroscience

Year:

2015

Language:

english

File:

PDF, 6.66 MB

english, 2015

26

Axonal mRNAs: Characterisation and role in the growth and regeneration of dorsal root ganglion axons and growth cones

Christina F. Vogelaar, Noreen M. Gervasi, Laura F. Gumy, David J. Story, Ruma Raha-Chowdhury, Kin-Mei Leung, Christine E. Holt, James W. Fawcett

Journal:

Molecular and Cellular Neuroscience

Year:

2009

Language:

english

File:

PDF, 1.10 MB

english, 2009

27

Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis.

Raha-Chowdhury, R, Bowen, D J, Burnett, A K, Worwood, M

Journal:

Journal of Medical Genetics

Year:

1995

Language:

english

File:

PDF, 1.23 MB

english, 1995

28

Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes

Olsson, K. Sigvard, Wålinder, Olof, Jansson, Ulf, Wilbe, Maria, Bondeson, Marie-Louise, Stattin, Eva-Lena, Raha-Chowdhury, Ruma, Williams, Roger

Journal:

Year:

2017

Language:

english

File:

PDF, 1.13 MB

english, 2017

29

The systemic iron-regulatory proteins hepcidin and ferroportin are reduced in the brain in Alzheimer’s disease

Raha, Animesh, Vaishnav, Radhika, Friedland, Robert, Bomford, Adrian, Raha-Chowdhury, Ruma

Journal:

Acta Neuropathologica Communications

Year:

2013

Language:

english

File:

PDF, 2.15 MB

english, 2013

30

Heparan sulphate proteoglycans in glia and in the normal and injured CNS: expression of sulphotransferases and changes in sulphation

Francesca Properzi, Rachel Lin, Jessica Kwok, Murali Naidu, Toin H. Van Kuppevelt, Gerdy B. Ten Dam, Luiz M. Camargo, Ruma Raha-Chowdhury, Yoko Furukawa, Tadahisa Mikami, Kazuyuki Sugahara, James W. F

Journal:

European Journal of Neuroscience

Year:

2008

Language:

english

File:

PDF, 609 KB

english, 2008

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