| Year |
Citation |
Score |
| 2015 |
Holtz AM, Griffiths SC, Davis SJ, Bishop B, Siebold C, Allen BL. Secreted HHIP1 interacts with heparan sulfate and regulates Hedgehog ligand localization and function. The Journal of Cell Biology. 209: 739-58. PMID 26056142 DOI: 10.1083/Jcb.201411024 |
0.655 |
|
| 2015 |
Song JY, Holtz AM, Pinskey JM, Allen BL. Distinct structural requirements for CDON and BOC in the promotion of Hedgehog signaling. Developmental Biology. 402: 239-52. PMID 25848697 DOI: 10.1016/J.Ydbio.2015.03.015 |
0.67 |
|
| 2015 |
Mathew E, Zhang Y, Holtz AM, Kane KT, Song J, Allen BL, Magliano MPd. Abstract A51: Novel Hedgehog co-receptors in pancreatic cancer Cancer Research. 75. DOI: 10.1158/1538-7445.Panca2014-A51 |
0.664 |
|
| 2014 |
Mathew E, Zhang Y, Holtz AM, Kane KT, Song JY, Allen BL, Pasca di Magliano M. Dosage-dependent regulation of pancreatic cancer growth and angiogenesis by hedgehog signaling. Cell Reports. 9: 484-94. PMID 25310976 DOI: 10.1016/J.Celrep.2014.09.010 |
0.622 |
|
| 2014 |
Camp D, Haitian He B, Li S, Althaus IW, Holtz AM, Allen BL, Charron F, van Meyel DJ. Ihog and Boi elicit Hh signaling via Ptc but do not aid Ptc in sequestering the Hh ligand. Development (Cambridge, England). 141: 3879-88. PMID 25231763 DOI: 10.1242/Dev.103564 |
0.661 |
|
| 2014 |
Mathew E, Collins MA, Fernandez-Barrena MG, Holtz AM, Yan W, Hogan JO, Tata Z, Allen BL, Fernandez-Zapico ME, di Magliano MP. The transcription factor GLI1 modulates the inflammatory response during pancreatic tissue remodeling. The Journal of Biological Chemistry. 289: 27727-43. PMID 25104358 DOI: 10.1074/Jbc.M114.556563 |
0.59 |
|
| 2013 |
Holtz AM, Peterson KA, Nishi Y, Morin S, Song JY, Charron F, McMahon AP, Allen BL. Essential role for ligand-dependent feedback antagonism of vertebrate hedgehog signaling by PTCH1, PTCH2 and HHIP1 during neural patterning. Development (Cambridge, England). 140: 3423-34. PMID 23900540 DOI: 10.1242/Dev.095083 |
0.653 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2023 |
Gracia-Diaz C, Zhou Y, Yang Q, Maroofian R, Espana-Bonilla P, Lee CH, Zhang S, Padilla N, Fueyo R, Waxman EA, Lei S, Otrimski G, Li D, Sheppard SE, Mark P, ... ... Holtz AM, et al. Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders. Nature Communications. 14: 4109. PMID 37433783 DOI: 10.1038/s41467-023-39645-5 |
0.241 |
|
| 2019 |
Holtz AM, Harrington AW, McNamara ER, Kielian A, Soul JS, Martinez-Ojeda M, Levy PT. Expanding the phenotypic spectrum of Mabry Syndrome with novel PIGO gene variants associated with hyperphosphatasia, intractable epilepsy, and complex gastrointestinal and urogenital malformations. European Journal of Medical Genetics. 103802. PMID 31698102 DOI: 10.1016/J.Ejmg.2019.103802 |
0.222 |
|
| 2017 |
Cardenas V, DiPaola F, Adams SD, Holtz AM, Ahmad A. Acute Liver Failure Secondary to Neuroblastoma Amplified Sequence Deficiency. The Journal of Pediatrics. PMID 28410752 DOI: 10.1016/J.Jpeds.2017.03.040 |
0.207 |
|
| 2022 |
Holtz AM, Vancoil R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, Millan F, Person R, Guillen Sacoto MJ, Si Y, Wentzensen IM, Pugh J, Vasileiou G, Rieger M, et al. Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 35980381 DOI: 10.1016/j.gim.2022.07.005 |
0.188 |
|
| 2024 |
Koch I, Slovik M, Zhang Y, Liu B, Rennie M, Konz E, Cogne B, Daana M, Davids L, Diets IJ, Gold NB, Holtz AM, Isidor B, Mor-Shaked H, Neira Fresneda J, et al. variants underlying X-linked intellectual disability disrupt protein function via distinct mechanisms. Life Science Alliance. 7. PMID 38182161 DOI: 10.26508/lsa.202302258 |
0.18 |
|
| 2024 |
Shepherdson JL, Hutchison K, Don DW, McGillivray G, Choi TI, Allan CA, Amor DJ, Banka S, Basel DG, Buch LD, Carere DA, Carroll R, Clayton-Smith J, Crawford A, Dunø M, ... ... Holtz AM, et al. Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt. American Journal of Human Genetics. PMID 38325380 DOI: 10.1016/j.ajhg.2024.01.007 |
0.152 |
|
| 2023 |
Flanagan FO, Holtz AM, Vargas SO, Genetti CA, Schmitz-Abe K, Casey A, Kennedy JC, Raby BA, Mullen MP, Fishman MP, Agrawal PB. An intronic variant in TBX4 in a single family with variable and severe pulmonary manifestations. Npj Genomic Medicine. 8: 7. PMID 36878902 DOI: 10.1038/s41525-023-00350-3 |
0.08 |
|
| 2023 |
Gold NB, Adelson SM, Shah N, Williams S, Bick SL, Zoltick ES, Gold JI, Strong A, Ganetzky R, Roberts AE, Walker M, Holtz AM, Sankaran VG, Delmonte O, Tan W, et al. Perspectives of Rare Disease Experts on Newborn Genome Sequencing. Jama Network Open. 6: e2312231. PMID 37155167 DOI: 10.1001/jamanetworkopen.2023.12231 |
0.037 |
|
| Hide low-probability matches. |