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The Journal of Cell Biology
|
January 3, 2001
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice
I Richard, C Roudaut, S Marchand, et al.
Molecular Biology & Medicine
|
September 1, 1983
Instability of the human immunoglobulin heavy chain constant region locus indicated by different inherited chromosomal deletions
M P Lefranc, G Lefranc, G de Lange, et al.
Human Biology
|
January 5, 2002
A worldwide analysis of AG molecular diversity inferred from serology
A Sanchez-Mazas, E Bütler-Brunner, R Bütler, et al.
European Journal of Human Genetics : EJHG
|
January 10, 2002
Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations
M Medlej-Hashim, I Petit, S Adib, et al.
Genetika
|
April 9, 1998
[Genetic analysis of the South Altaian population of the Mendur-Sokkon village, Altai Republic]
O L Posukh, L P Osipova, Iu O Kashinskaia, et al.
Clinical Genetics
|
September 13, 2011
A novel deletion in ZBTB24 in a Lebanese family with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2
E Chouery, J Abou-Ghoch, S Corbani, et al.
Nature Medicine
|
May 6, 1999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2A
S Baghdiguian, M Martin, I Richard, et al.
Science (New York, N.Y.)
|
June 26, 2001
Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance
S A Tishkoff, R Varkonyi, N Cahinhinan, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations
I Mansour, V Delague, C Cazeneuve, et al.
Annals of Human Genetics
|
April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspective
C Capelli, N Redhead, V Romano, et al.
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of 18
Search research articles
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Showing results (161-170 of 172) with videos related to
Sort By:
Page
of 18
The Journal of Cell Biology
|
January 3, 2001
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice
I Richard, C Roudaut, S Marchand, et al.
Molecular Biology & Medicine
|
September 1, 1983
Instability of the human immunoglobulin heavy chain constant region locus indicated by different inherited chromosomal deletions
M P Lefranc, G Lefranc, G de Lange, et al.
Human Biology
|
January 5, 2002
A worldwide analysis of AG molecular diversity inferred from serology
A Sanchez-Mazas, E Bütler-Brunner, R Bütler, et al.
European Journal of Human Genetics : EJHG
|
January 10, 2002
Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations
M Medlej-Hashim, I Petit, S Adib, et al.
Genetika
|
April 9, 1998
[Genetic analysis of the South Altaian population of the Mendur-Sokkon village, Altai Republic]
O L Posukh, L P Osipova, Iu O Kashinskaia, et al.
Clinical Genetics
|
September 13, 2011
A novel deletion in ZBTB24 in a Lebanese family with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2
E Chouery, J Abou-Ghoch, S Corbani, et al.
Nature Medicine
|
May 6, 1999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2A
S Baghdiguian, M Martin, I Richard, et al.
Science (New York, N.Y.)
|
June 26, 2001
Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance
S A Tishkoff, R Varkonyi, N Cahinhinan, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations
I Mansour, V Delague, C Cazeneuve, et al.
Annals of Human Genetics
|
April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspective
C Capelli, N Redhead, V Romano, et al.
Page
of 18