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PubMed 28711606 Ovarian aromatase loss-of-function mutant medaka undergo ovary degeneration and partial female-to-male sex reversal after puberty. Although estrogens have been generally considered to play a critical 1.22 KB 2019-09-23 28 12
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PubMed 28711549 A case of hypocholesterolemia and steatosis in a carrier of a PCSK9 loss-of-function mutation and polymorphisms predisposing to nonalcoholic fatty liver disease. We report a new case of hypobetalipopr 1.02 KB 2025-10-02 31 16
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PubMed 28708837 Extracellular inhibitors can attenuate tumorigenic Wnt pathway activity in adenomatous polyposis coli mutants: Predictions of a validated mathematical model. BACKGROUND: Despite considerable investiga 2.2 KB 2019-09-23 30 19
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PubMed 28701352 Calcium pumps and interacting BON1 protein modulate calcium signature, stomatal closure, and plant immunity. Calcium signaling is essential for environmental responses including immune responses. Here 1.39 KB 2019-09-23 27 28
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PubMed 28697784 Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers. BACKGROUND: Limb-girdle muscular dystrophies (LGMDs) are a heterogeneous group of inherit 1.31 KB 2019-09-23 28 16
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PubMed 28683731 Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by null LAMB2 mutations. BACKGROUND: Congenital nephrotic syndrome (CNS) is a rare disorder caused by v 1.95 KB 2019-09-23 28 9
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PubMed 28667273 Natural and induced loss of function mutations in SlMBP21 MADS-box gene led to jointless-2 phenotype in tomato. Abscission is the mechanism by which plants disconnect unfertilized flowers, ripe fruits 1.44 KB 2019-09-23 39 7
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PubMed 28662729 The moving junction protein RON4, although not critical, facilitates host cell invasion and stabilizes MJ members. Toxoplasma gondii is an obligate intracellular parasite of phylum Apicomplexa. To fac 1.03 KB 2019-09-23 27 18
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PubMed 28659290 Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20). 97 Bytes 2019-09-23 27 7
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PubMed 28650109 Inducible activation of FGFR2 in adult mice promotes bone formation after bone marrow ablation. Apert syndrome is one of the most severe craniosynostoses, resulting from gain-of-function mutations in 1.64 KB 2019-09-23 29 53
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