Michael Z. Ludwig to Humans
This is a "connection" page, showing publications Michael Z. Ludwig has written about Humans.
Connection Strength
0.119
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An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome. Int J Mol Med. 2013 Jul; 32(1):174-8.
Score: 0.014
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Four additional CLCN5 exons encode a widely expressed novel long CLC-5 isoform but fail to explain Dent's phenotype in patients without mutations in the short variant. Kidney Blood Press Res. 2003; 26(3):176-84.
Score: 0.007
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Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadias. Scand J Urol Nephrol. 2003; 37(6):498-501.
Score: 0.007
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A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length? Hum Genet. 2002 May; 110(5):488-94.
Score: 0.007
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Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia. PLoS One. 2020; 15(6):e0234246.
Score: 0.006
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The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia. Nat Struct Biol. 1999 Apr; 6(4):359-65.
Score: 0.005
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Autophagy Inhibition Mediates Apoptosis Sensitization in Cancer Therapy by Relieving FOXO3a Turnover. Dev Cell. 2018 03 12; 44(5):555-565.e3.
Score: 0.005
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ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development. Sci Rep. 2017 02 08; 7:42170.
Score: 0.005
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Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. Psychiatr Genet. 2016 12; 26(6):293-296.
Score: 0.005
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Molecular basis for dysfunction of some mutant forms of methylmalonyl-CoA mutase: deductions from the structure of methionine synthase. Proc Natl Acad Sci U S A. 1996 May 28; 93(11):5550-5.
Score: 0.004
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Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association. Hum Mutat. 2015 Dec; 36(12):1150-4.
Score: 0.004
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WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish. Hum Mol Genet. 2015 Sep 15; 24(18):5069-78.
Score: 0.004
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Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy. PLoS Genet. 2015 Mar; 11(3):e1005024.
Score: 0.004
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Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder. Hum Mol Genet. 2014 Oct 15; 23(20):5536-44.
Score: 0.004
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Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region. Birth Defects Res A Clin Mol Teratol. 2014 Jun; 100(6):512-7.
Score: 0.004
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Genetic complexity in a Drosophila model of diabetes-associated misfolded human proinsulin. Genetics. 2014 Feb; 196(2):539-55.
Score: 0.004
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Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin. Genetics. 2014 Feb; 196(2):557-67.
Score: 0.004
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VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis. Clin Dysmorphol. 2012 Oct; 21(4):191-195.
Score: 0.003
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Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadias. Gene. 2012 Sep 15; 506(2):392-5.
Score: 0.003
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Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. Am J Hum Genet. 2011 Nov 11; 89(5):668-74.
Score: 0.003
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p63 (TP73L) a key player in embryonic urogenital development with significant dysregulation in human bladder exstrophy tissue. Int J Mol Med. 2010 Dec; 26(6):861-7.
Score: 0.003
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Embryonic expression of the cysteine rich protein 61 (CYR61) gene: A candidate for the development of human epispadias. Birth Defects Res A Clin Mol Teratol. 2010 Jul; 88(7):546-50.
Score: 0.003
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Analysis of Drosophila segmentation network identifies a JNK pathway factor overexpressed in kidney cancer. Science. 2009 Feb 27; 323(5918):1218-22.
Score: 0.003
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Low frequency of imprinting defects in ICSI children born small for gestational age. Eur J Hum Genet. 2009 Jan; 17(1):22-9.
Score: 0.003
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R561C missense mutation in the SMARCAL1 gene associated with mild Schimke immuno-osseous dysplasia. Pediatr Nephrol. 2005 Dec; 20(12):1724-8.
Score: 0.002
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Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model. Hum Mol Genet. 2004 Nov 15; 13(22):2841-51.
Score: 0.002
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Emergence of epidemic O'nyong-nyong fever in Uganda after a 35-year absence: genetic characterization of the virus. Virology. 1998 Dec 05; 252(1):258-68.
Score: 0.001