N Mohandas
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Explore the profile of N Mohandas including associated specialties, affiliations and a list of published articles.
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246
Citations
5823
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Recent Articles
1.
Narla J, Mohandas N
Int J Lab Hematol
. 2017 Apr;
39 Suppl 1:47-52.
PMID: 28447420
Significant advances have been made in our understanding of the structural basis for altered cell function in various inherited red cell membrane disorders with reduced red cell survival and resulting...
2.
John B, Swaminathan S, Venkatakrishnan L, Singh G, Krishnaveni G, Mohandas N, et al.
Indian J Surg
. 2015 May;
77(Suppl 1):125-7.
PMID: 25972670
Infected pancreatic necrosis (IPN) is associated with high morbidity and mortality. It is increasingly being recognized that noninvasive management, radiological guided drainage, and minimally invasive procedures rather than the traditionally...
3.
Moniz H, Gastou M, Leblanc T, Hurtaud C, Cretien A, Lecluse Y, et al.
Cell Death Dis
. 2012 Jul;
3:e356.
PMID: 22833095
Diamond-Blackfan anemia (DBA) is caused by aberrant ribosomal biogenesis due to ribosomal protein (RP) gene mutations. To develop mechanistic understanding of DBA pathogenesis, we studied CD34⁺ cells from peripheral blood...
4.
Meller J, Malinin N, Panigrahi S, Kerr B, Patil A, Ma Y, et al.
J Thromb Haemost
. 2012 May;
10(7):1397-408.
PMID: 22564402
Background: Kindlin-3 is a novel integrin activator in hematopoietic cells, and its deficiency leads to immune problems and severe bleeding, known as leukocyte adhesion deficiency III (LAD-III). Our current understanding...
5.
An X, Mohandas N
Transfus Clin Biol
. 2010 Aug;
17(3):197-9.
PMID: 20674435
Malaria is the most serious and widespread parasitic disease of humans, with up to 500 million people being infected each year with malaria parasites and a million individuals, predominantly infants...
6.
Da Costa L, Moniz H, Simansour M, Tchernia G, Mohandas N, Leblanc T
Transfus Clin Biol
. 2010 Jul;
17(3):112-9.
PMID: 20655265
Diamond-Blackfan anemia is a rare inherited bone marrow failure syndrome (five to seven cases per million live births) characterized by an aregenerative, usually macrocytic anemia with an absence or less...
7.
Mohandas N, An X
Transfus Clin Biol
. 2006 Apr;
13(1-2):29-30.
PMID: 16581279
No abstract available.
8.
Nicolas V, Mouro-Chanteloup I, Lopez C, Gane P, Gimm A, Mohandas N, et al.
Transfus Clin Biol
. 2006 Apr;
13(1-2):23-8.
PMID: 16580865
We summarize the different experimental approaches which provide evidence that direct interaction of Rh and RhAG to ankyrin-R constitutes, together with the AE-1 (Band 3)-ankyrin-protein 4.2 and GPC-protein 4.1-p55 complexes,...
9.
Wandersee N, Birkenmeier C, Gifford E, Mohandas N, Barker J
Hematol J
. 2002 Mar;
1(4):235-42.
PMID: 11920196
Introduction: Spectrin, a heterodimer of alpha- and beta-subunits, is the major protein component of the red blood cell membrane skeleton. The mouse mutation, sph, causes an alpha-spectrin-deficient hereditary spherocytosis with...
10.
Tchernia G, Delhommeau F, Perrotta S, Cynober T, Bader-Meunier B, Nobili B, et al.
Hematol J
. 2002 Mar;
1(3):146-52.
PMID: 11920183
Introduction: In hereditary spherocytosis, erythropoiesis has been described as 'sluggish' during the first months of life. The lack of appropriate erythropoietic response to compensate for increased red cell destruction necessitates...