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source DB |
source ID
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text
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size
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updated at |
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# proj.
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# Ann.
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updated_at |
| PubMed |
28589954 |
WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-medi |
1.18 KB |
2019-09-23 |
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38 |
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13 |
-
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| PubMed |
28592524 |
Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects.
BACKGROUND: Con |
1.44 KB |
2019-09-23 |
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28 |
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9 |
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| PubMed |
28597146 |
Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency.
Germline heterozygous gain-of- |
2.32 KB |
2019-09-23 |
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30 |
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20 |
-
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| PubMed |
28627419 |
ARX polyalanine expansion mutations lead to migration impediment in the rostral cortex coupled with |
1.92 KB |
2019-09-23 |
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28 |
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21 |
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| PubMed |
28650109 |
Inducible activation of FGFR2 in adult mice promotes bone formation after bone marrow ablation.
Aper |
1.64 KB |
2019-09-23 |
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29 |
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53 |
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| PubMed |
28659290 |
Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20).
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97 Bytes |
2019-09-23 |
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27 |
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7 |
-
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| PubMed |
28662729 |
The moving junction protein RON4, although not critical, facilitates host cell invasion and stabiliz |
1.03 KB |
2019-09-23 |
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27 |
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18 |
-
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| PubMed |
28667273 |
Natural and induced loss of function mutations in SlMBP21 MADS-box gene led to jointless-2 phenotype |
1.44 KB |
2019-09-23 |
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37 |
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7 |
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| PubMed |
28683731 |
Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by |
1.95 KB |
2019-09-23 |
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28 |
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9 |
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| PubMed |
28697784 |
Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston |
1.31 KB |
2019-09-23 |
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28 |
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16 |
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