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Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America.
- Published in:
- Human Genetics, 2001, v. 108, n. 1, p. 51, doi. 10.1007/s004390000440
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- Publication type:
- Article
A new acro-osteolysis syndrome caused by duplications including PTHLH.
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- Journal of Human Genetics, 2014, v. 59, n. 9, p. 484, doi. 10.1038/jhg.2014.58
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- Publication type:
- Article
Molecular Heterogeneity of Urinary Proteins in Wild House Mouse Populations.
- Published in:
- Rapid Communications in Mass Spectrometry: RCM, 1997, v. 11, n. 7, p. 786, doi. 10.1002/(SICI)1097-0231(19970422)11:7<786::AID-RCM876>3.0.CO;2-8
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- Publication type:
- Article
The College Administrator's Survival Guide.
- Published in:
- 2007
- By:
- Publication type:
- Book Review
Comparative Proteomics Reveals Evidence for Evolutionary Diversification of Rodent Seminal Fluid and Its Functional Significance in Sperm Competition.
- Published in:
- Molecular Biology & Evolution, 2009, v. 26, n. 1, p. 189
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- Publication type:
- Article
Individual recognition in mice mediated by major urinary proteins.
- Published in:
- Nature, 2001, v. 414, n. 6864, p. 631, doi. 10.1038/414631a
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- Publication type:
- Article
Communal breeding affects offspring behaviours associated with a competitive social environment.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35089-w
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- Publication type:
- Article
Roborovskin, a Lipocalin in the Urine of the Roborovski Hamster, Phodopus roborovskii.
- Published in:
- Chemical Senses, 2010, v. 35, n. 8, p. 675, doi. 10.1093/chemse/bjq060
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- Publication type:
- Article
Host Range and Genetic Diversity of Arenaviruses in Rodents, United Kingdom.
- Published in:
- Emerging Infectious Diseases, 2008, v. 14, n. 9, p. 1455, doi. 10.3201/eid1409.080209
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- Publication type:
- Article
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 14, p. 2172, doi. 10.1093/hmg/ddn116
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- Publication type:
- Article
Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 5, p. 610, doi. 10.1038/ejhg.2014.162
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- Publication type:
- Article
The major urinary protein system in the rat.
- Published in:
- Biochemical Society Transactions, 2014, v. 42, n. 4, p. 886, doi. 10.1042/BST20140083
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- Publication type:
- Article
The complexity of protein semiochemistry in mammals.
- Published in:
- Biochemical Society Transactions, 2014, v. 42, n. 4, p. 837, doi. 10.1042/BST20140133
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- Publication type:
- Article
Comparative study of the molecular variation between 'central' and 'peripheral' MUPs and significance for behavioural signalling.
- Published in:
- Biochemical Society Transactions, 2014, v. 42, n. 4, p. 866, doi. 10.1042/BST20140082
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- Publication type:
- Article
Book reviews.
- Published in:
- 1996
- By:
- Publication type:
- Book Review
Scent wars: the chemobiology of competitive signalling in mice.
- Published in:
- BioEssays, 2004, v. 26, n. 12, p. 1288, doi. 10.1002/bies.20147
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- Publication type:
- Article
Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3.
- Published in:
- 2011
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- Publication type:
- Case Study
Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 9, p. 1019, doi. 10.1038/sj.ejhg.5201456
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- Publication type:
- Article
A refined physical and transcriptional map of the SPG9 locus on 10q23.3–q24.2.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 10, p. 777, doi. 10.1038/sj.ejhg.5200546
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- Publication type:
- Article
Women managing women: An holistic relational approach to managing relationships at work.
- Published in:
- Journal of Management & Organization, 2018, v. 24, n. 4, p. 500, doi. 10.1017/jmo.2017.10
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- Publication type:
- Article
Effect of polymorphisms on ligand binding by mouse major urinary proteins.
- Published in:
- Protein Science: A Publication of the Protein Society, 2001, v. 10, n. 2, p. 411, doi. 10.1110/ps.31701
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- Publication type:
- Article
Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2).
- Published in:
- 2003
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- Publication type:
- Letter
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.
- Published in:
- Nature Genetics, 2006, v. 38, n. 9, p. 1038, doi. 10.1038/ng1862
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- Publication type:
- Article
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
- Published in:
- Nature Genetics, 2004, v. 36, n. 9, p. 955, doi. 10.1038/ng1407
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- Publication type:
- Article
Persistent hyperinsulinaemic hypoglycaemia in children with Rubinstein–Taybi syndrome.
- Published in:
- European Journal of Endocrinology, 2019, v. 181, n. 2, p. 121, doi. 10.1530/EJE-19-0119
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- Publication type:
- Article
Rapid identification of species, sex and maturity by mass spectrometric analysis of animal faeces.
- Published in:
- BMC Biology, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12915-019-0686-9
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- Publication type:
- Article
Applying remotely sensed habitat descriptors to assist reintroduction programs: A case study in the hazel dormouse.
- Published in:
- Conservation Science & Practice, 2021, v. 3, n. 12, p. 1, doi. 10.1111/csp2.544
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- Publication type:
- Article
Sotos Syndrome Presenting with Neonatal Hyperinsulinaemic Hypoglycaemia, Extensive Thrombosis, and Multisystem Involvement.
- Published in:
- Hormone Research in Paediatrics, 2019, v. 92, n. 1, p. 64, doi. 10.1159/000496545
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- Publication type:
- Article
Enhancing collaboration in the UK animal welfare research community.
- Published in:
- Veterinary Record: Journal of the British Veterinary Association, 2016, v. 178, n. 6, p. 138, doi. 10.1136/vr.i682
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- Publication type:
- Article
Mutations in MAGEL2 and L1CAM Are Associated With Congenital Hypopituitarism and Arthrogryposis.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2019, v. 104, n. 12, p. 5737, doi. 10.1210/jc.2019-00631
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- Publication type:
- Article
Syndromic associations with congenital anomalies of the fetal thorax and abdomen.
- Published in:
- Prenatal Diagnosis, 2008, v. 28, n. 7, p. 676, doi. 10.1002/pd.2023
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- Publication type:
- Article
The Structure, Stability and Pheromone Binding of the Male Mouse Protein Sex Pheromone Darcin.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0108415
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- Publication type:
- Article
Reducing Mouse Anxiety during Handling: Effect of Experience with Handling Tunnels.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066401
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- Publication type:
- Article
Composition and Function of Haemolymphatic Tissues in the European Common Shrew.
- Published in:
- PLoS ONE, 2008, v. 3, n. 10, p. 1, doi. 10.1371/journal.pone.0003413
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- Publication type:
- Article
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.
- Published in:
- Nature Genetics, 2000, v. 24, n. 4, p. 387, doi. 10.1038/74224
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- Publication type:
- Article
Protein turnover: Measurement of proteome dynamics by whole animal metabolic labelling with stable isotope labelled amino acids.
- Published in:
- Proteomics, 2012, v. 12, n. 8, p. 1194, doi. 10.1002/pmic.201100556
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- Publication type:
- Article
De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder.
- Published in:
- Human Genetics, 2018, v. 137, n. 5, p. 375, doi. 10.1007/s00439-018-1887-y
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- Publication type:
- Article
Optimising reliability of mouse performance in behavioural testing: the major role of non-aversive handling.
- Published in:
- Scientific Reports, 2017, p. 44999, doi. 10.1038/srep44999
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- Publication type:
- Article
Molecular heterogeneity in major urinary proteins of Mus musculus subspecies: potential candidates involved in speciation.
- Published in:
- Scientific Reports, 2017, p. 44992, doi. 10.1038/srep44992
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- Publication type:
- Article
Characterisation of urinary WFDC12 in small nocturnal basal primates, mouse lemurs (Microcebus spp.).
- Published in:
- Scientific Reports, 2017, p. 42940, doi. 10.1038/srep42940
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- Publication type:
- Article
The male sex pheromone darcin stimulates hippocampal neurogenesis and cell proliferation in the subventricular zone in female mice.
- Published in:
- Frontiers in Behavioral Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fnbeh.2015.00106
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- Publication type:
- Article
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-63
- By:
- Publication type:
- Article
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Taming anxiety in laboratory mice.
- Published in:
- Nature Methods, 2010, v. 7, n. 10, p. 825, doi. 10.1038/nmeth.1500
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- Publication type:
- Article
Rapid identification of mosquito species and age by mass spectrometric analysis.
- Published in:
- BMC Biology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12915-022-01508-8
- By:
- Publication type:
- Article
Rapid identification of mosquito species and age by mass spectrometric analysis.
- Published in:
- BMC Biology, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12915-022-01508-8
- By:
- Publication type:
- Article
A forkhead-domain gene is mutated in a severe speech and language disorder.
- Published in:
- Nature, 2001, v. 413, n. 6855, p. 519, doi. 10.1038/35097076
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- Publication type:
- Article
Fanconi Anemia: Examining Guidelines for Testing All Patients with Hand Anomalies Using a Machine Learning Approach.
- Published in:
- Children, 2022, v. 9, n. 1, p. 85, doi. 10.3390/children9010085
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- Publication type:
- Article
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
- Published in:
- Nucleic Acids Research, 2014, v. 42, n. D1, p. D966
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- Publication type:
- Article
Systematic review and meta-analysis of the association between childhood overweight and obesity and primary school diet and physical activity policies.
- Published in:
- International Journal of Behavioral Nutrition & Physical Activity, 2013, v. 10, p. 101, doi. 10.1186/1479-5868-10-101
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- Publication type:
- Article