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Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
May 18, 2001
A novel gene, tendin, is strongly expressed in tendons and ligaments and shows high homology with chondromodulin-I
O Brandau, A Meindl, R Fässler, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
February 27, 2001
Stage-and tissue-specific expression of a Col2a1-Cre fusion gene in transgenic mice
K Sakai, L Hiripi, V Glumoff, et al.
European Journal of Human Genetics : EJHG
|
November 5, 1998
UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2
O Brandau, G Nyakatura, K B Jedele, et al.
Transplantation Proceedings
|
August 1, 1993
Influence of SOD, catalase, and epoprostenol on 24-hour liver preservation in pigs
H P Lemmens, M R Schön, G Blumhardt, et al.
Clinical Genetics
|
July 31, 2018
A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab children
H Yavuz, A M Bertoli-Avella, M Alfadhel, et al.
Human Molecular Genetics
|
November 11, 1999
Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)
O Brandau, V Schuster, M Weiss, et al.
Pediatrics
|
January 31, 1998
Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course
E Holinski-Feder, M Weiss, O Brandau, et al.
British Journal of Haematology
|
February 26, 2000
Recurrent B-cell non-Hodgkin's lymphoma in two brothers with X-linked lymphoproliferative disease without evidence for Epstein-Barr virus infection
B Strahm, K Rittweiler, U Duffner, et al.
Nature Genetics
|
November 4, 2000
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
C M Pusch, C Zeitz, O Brandau, et al.
Nucleic Acids Research
|
February 21, 1998
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, O Brandau, L J Brandén, et al.
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Search research articles
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Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
May 18, 2001
A novel gene, tendin, is strongly expressed in tendons and ligaments and shows high homology with chondromodulin-I
O Brandau, A Meindl, R Fässler, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
February 27, 2001
Stage-and tissue-specific expression of a Col2a1-Cre fusion gene in transgenic mice
K Sakai, L Hiripi, V Glumoff, et al.
European Journal of Human Genetics : EJHG
|
November 5, 1998
UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2
O Brandau, G Nyakatura, K B Jedele, et al.
Transplantation Proceedings
|
August 1, 1993
Influence of SOD, catalase, and epoprostenol on 24-hour liver preservation in pigs
H P Lemmens, M R Schön, G Blumhardt, et al.
Clinical Genetics
|
July 31, 2018
A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab children
H Yavuz, A M Bertoli-Avella, M Alfadhel, et al.
Human Molecular Genetics
|
November 11, 1999
Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)
O Brandau, V Schuster, M Weiss, et al.
Pediatrics
|
January 31, 1998
Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course
E Holinski-Feder, M Weiss, O Brandau, et al.
British Journal of Haematology
|
February 26, 2000
Recurrent B-cell non-Hodgkin's lymphoma in two brothers with X-linked lymphoproliferative disease without evidence for Epstein-Barr virus infection
B Strahm, K Rittweiler, U Duffner, et al.
Nature Genetics
|
November 4, 2000
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
C M Pusch, C Zeitz, O Brandau, et al.
Nucleic Acids Research
|
February 21, 1998
BTKbase, mutation database for X-linked agammaglobulinemia (XLA)
M Vihinen, O Brandau, L J Brandén, et al.
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of 2