| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1036235331 |
| P356 | DOI | 10.1186/1471-2164-8-92 |
| P932 | PMC publication ID | 1855325 |
| P698 | PubMed publication ID | 17407603 |
| P5875 | ResearchGate publication ID | 6413553 |
| P50 | author | Stephen W. Scherer | Q7610775 |
| Jeffrey R MacDonald | Q61299957 | ||
| P2093 | author name string | Benjamin A Alman | |
| Catherine F Li | |||
| Christopher Kandel | |||
| Jocelyn Ray | |||
| Kimberly Lau | |||
| Rachel Koffman | |||
| Robert Y Wei | |||
| Sherilyn Bell | |||
| P2860 | cites work | A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis | Q24302045 |
| Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences | Q24336098 | ||
| Multiple sequence alignment with the Clustal series of programs | Q24672842 | ||
| Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 | ||
| Oligomeric structure of the human EphB2 receptor SAM domain | Q27766879 | ||
| A system for stable expression of short interfering RNAs in mammalian cells | Q27860875 | ||
| The RNA-binding SAM domain of Smaug defines a new family of post-transcriptional regulators | Q27934943 | ||
| PROSITE: a documented database using patterns and profiles as motif descriptors | Q28201713 | ||
| A molecular timescale for vertebrate evolution | Q29547791 | ||
| PHD: predicting one-dimensional protein structure by profile-based neural networks | Q29614390 | ||
| CD-Search: protein domain annotations on the fly | Q29615328 | ||
| Database resources of the National Center for Biotechnology | Q29618892 | ||
| The LIM-only protein FHL2 interacts with beta-catenin and promotes differentiation of mouse myoblasts | Q31113643 | ||
| Gas6 induces growth, beta-catenin stabilization, and T-cell factor transcriptional activation in contact-inhibited C57 mammary cells | Q33967129 | ||
| Recent improvements to the PROSITE database | Q34927063 | ||
| Structural dynamics of eukaryotic chromosome evolution | Q35195593 | ||
| Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease | Q35649549 | ||
| Tcf-3 expression and beta-catenin mediated transcriptional activation in aggressive fibromatosis (desmoid tumour). | Q36623084 | ||
| Recent segmental duplications in the working draft assembly of the brown Norway rat. | Q37322204 | ||
| Plasminogen activator inhibitor-1 (PAI-1) modifies the formation of aggressive fibromatosis (desmoid tumor). | Q38331352 | ||
| Analysis of canonical and non-canonical splice sites in mammalian genomes | Q39597422 | ||
| Adenomatous polyposis coli gene mutation alters proliferation through its beta-catenin-regulatory function in aggressive fibromatosis (desmoid tumor). | Q41843537 | ||
| Increased beta-catenin protein and somatic APC mutations in sporadic aggressive fibromatoses (desmoid tumors). | Q42082840 | ||
| Human-mouse comparative mapping of the genomic region containing CDK6: localization of an evolutionary breakpoint | Q42604416 | ||
| Matrix metalloproteinase activity modulates tumor size, cell motility, and cell invasiveness in murine aggressive fibromatosis. | Q47410463 | ||
| ScanProsite: a reference implementation of a PROSITE scanning tool | Q47638393 | ||
| Aggressive fibromatosis (desmoid tumor) is a monoclonal disorder. | Q50962782 | ||
| Cyclooxygenase-two (COX-2) modulates proliferation in aggressive fibromatosis (desmoid tumor). | Q52136489 | ||
| Genetic deletion of receptor for hyaluronan-mediated motility (Rhamm) attenuates the formation of aggressive fibromatosis (desmoid tumor). | Q54517252 | ||
| Murine segmental duplications are hot spots for chromosome and gene evolution | Q57304613 | ||
| Immunocytochemical analysis of chromaffin cell proliferation in vitro | Q67517606 | ||
| Retinal VEGF mRNA measured by SYBR green I fluorescence: A versatile approach to quantitative PCR | Q73053086 | ||
| Why mice have lost genes for COL21A1, STK17A, GPR145 and AHRI: evidence for gene deletion at evolutionary breakpoints in the rodent lineage | Q80457864 | ||
| P4510 | describes a project that uses | ImageQuant | Q112270642 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | aggressive fibromatosis | Q475086 |
| P304 | page(s) | 92 | |
| P577 | publication date | 2007-01-01 | |
| P1433 | published in | BMC Genomics | Q15765854 |
| P1476 | title | Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouse | |
| P478 | volume | 8 |
| Q38226741 | -7/7q- syndrome in myeloid-lineage hematopoietic malignancies: attempts to understand this complex disease entity |
| Q52673585 | A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing. |
| Q49979583 | A paralogous pair of mammalian host restriction factors form a critical host barrier against poxvirus infection. |
| Q38718110 | An interaction domain in human SAMD9 is essential for myxoma virus host-range determinant M062 antagonism of host anti-viral function. |
| Q33494984 | Anti-oncogenic and pro-differentiation effects of clorgyline, a monoamine oxidase A inhibitor, on high grade prostate cancer cells |
| Q37005060 | Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L. |
| Q34161852 | C7L family of poxvirus host range genes inhibits antiviral activities induced by type I interferons and interferon regulatory factor 1. |
| Q51887919 | Conceptus-induced changes in the endometrial transcriptome: how soon does the cow know she is pregnant? |
| Q88654486 | Decoding the Emerging Patterns Exhibited in Non-coding RNAs Characteristic of Lung Cancer with Regard to their Clinical Significance |
| Q37507342 | Disorders of phosphate homeostasis and tissue mineralisation |
| Q26865249 | Ectopic mineralization disorders of the extracellular matrix of connective tissue: molecular genetics and pathomechanisms of aberrant calcification |
| Q39305159 | Epipodial Tentacle Gene Expression and Predetermined Resilience to Summer Mortality in the Commercially Important Greenlip Abalone, Haliotis laevigata |
| Q28681331 | Evolution and divergence of the mammalian SAMD9/SAMD9L gene family |
| Q37327002 | Familial tumoral calcinosis and the role of O-glycosylation in the maintenance of phosphate homeostasis |
| Q35203191 | Familial tumoral calcinosis: from characterization of a rare phenotype to the pathogenesis of ectopic calcification |
| Q38353654 | Functional characterization of SAMD9, a protein deficient in normophosphatemic familial tumoral calcinosis |
| Q40331582 | Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms |
| Q24328884 | Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7 |
| Q64126564 | Identification of CP77 as the third orthopoxvirus SAMD9 and SAMD9L inhibitor with a unique specificity for a rodent SAMD9L |
| Q93012659 | Identification of SAMD9L as a susceptibility locus for intravenous immunoglobulin resistance in Kawasaki disease by genome-wide association analysis |
| Q28397240 | Long-term exposure of MCF-7 breast cancer cells to ethanol stimulates oncogenic features |
| Q46262683 | Longitudinal system-based analysis of transcriptional responses to type I interferons |
| Q30499249 | M062 is a host range factor essential for myxoma virus pathogenesis and functions as an antagonist of host SAMD9 in human cells |
| Q36986492 | Mineralization/anti-mineralization networks in the skin and vascular connective tissues |
| Q36054790 | Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphataemic familial tumoral calcinosis |
| Q35203230 | Normophosphatemic familial tumoral calcinosis is caused by deleterious mutations in SAMD9, encoding a TNF-alpha responsive protein |
| Q36610899 | Novel molecular therapies for heritable skin disorders |
| Q48299262 | Ontogenetic changes in embryonic and brain gene expression in progeny produced from migratory and resident Oncorhynchus mykiss |
| Q24295009 | Poly-ADP ribosylation of Miki by tankyrase-1 promotes centrosome maturation |
| Q104570478 | Proteomic profile of vitreous in patients with tubercular uveitis |
| Q54256504 | SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies. |
| Q33970149 | SAMD9L inactivation promotes cell proliferation via facilitating G1-S transition in hepatitis B virus-associated hepatocellular carcinoma |
| Q60912238 | SOX2 participates in spermatogenesis of Zhikong scallop Chlamys farreri |
| Q33617141 | Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans. |
| Q35930739 | Sterile α Motif Domain Containing 9 Is a Novel Cellular Interacting Partner to Low-Risk Type Human Papillomavirus E6 Proteins |
| Q35215295 | The Samd9L gene: transcriptional regulation and tissue-specific expression in mouse development |
| Q30853575 | The complex domain architecture of SAMD9 family proteins, predicted STAND-like NTPases, suggests new links to inflammation and apoptosis |
| Q36427971 | The poxvirus C7L host range factor superfamily |
| Q55061507 | Transcriptomic response of breast cancer cells to anacardic acid. |
| Q36894189 | Zebrafish models for ectopic mineralization disorders: practical issues from morpholino design to post-injection observations |
| Q30427003 | Zebrafish: a model system to study heritable skin diseases |
| Q42538506 | miR-96 induces cisplatin chemoresistance in non-small cell lung cancer cells by downregulating SAMD9. |
| Q36331373 | ΔNp63α represses anti-proliferative genes via H2A.Z deposition. |
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