Found: 31
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Hormone-mediated growth dynamics of the barley pericarp as revealed by magnetic resonance imaging and transcript profiling.
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- Journal of Experimental Botany, 2015, v. 66, n. 21, p. 6927, doi. 10.1093/jxb/erv397
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- Article
Metabolic and transcriptional transitions in barley glumes reveal a role as transitory resource buffers during endosperm filling.
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- Journal of Experimental Botany, 2015, v. 66, n. 5, p. 1397, doi. 10.1093/jxb/eru492
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- Article
Gibberellin-to-abscisic acid balances govern development and differentiation of the nucellar projection of barley grains.
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- Journal of Experimental Botany, 2014, v. 65, n. 18, p. 5291, doi. 10.1093/jxb/eru289
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- Article
MRI diagnosis of spontaneous intraventricular tension‐pneumocephalus in a 10‐month‐old male Saarloos Wolfdog.
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- Veterinary Radiology & Ultrasound, 2022, v. 63, n. 3, p. e20, doi. 10.1111/vru.13040
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Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney Malformations.
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- Nephrology Dialysis Transplantation, 2022, v. 37, n. 12, p. 2351, doi. 10.1093/ndt/gfac207
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- Article
Transposition of a bacterial insertion sequence in chloroplasts.
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- Plant Journal, 2009, v. 58, n. 3, p. 423, doi. 10.1111/j.1365-313X.2009.03787.x
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- Article
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.
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- Kidney International, 2014, v. 85, n. 6, p. 1310, doi. 10.1038/ki.2013.417
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- Article
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.
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- Kidney International, 2014, v. 85, n. 6, p. 1429, doi. 10.1038/ki.2013.508
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- Article
Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies.
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- Kidney International, 2014, v. 85, n. 4, p. 880, doi. 10.1038/ki.2013.450
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- Article
3T MRI characteristics of the palatine tonsil in brachycephalic dogs.
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- Veterinary Record: Journal of the British Veterinary Association, 2022, v. 190, n. 5, p. 1, doi. 10.1002/vetr.1077
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- Article
ON CONJUGATES OF COLLATZ-TYPE MAPPINGS.
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- International Journal of Number Theory, 2008, v. 4, n. 1, p. 117, doi. 10.1142/S1793042108001237
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- Article
Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT).
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- Molecular & Cellular Pediatrics, 2021, v. 8, n. 1, p. 1, doi. 10.1186/s40348-021-00112-0
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Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.
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- Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01215-1
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- Article
Microtubule Associated Protein 1b (MAP1B) Is a Marker of the Microtubular Cytoskeleton in Podocytes but Is Not Essential for the Function of the Kidney Filtration Barrier in Mice.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0140116
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- Article
A putative role for amino acid permeases in sink-source communication of barley tissues uncovered by RNA-seq.
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- BMC Plant Biology, 2012, v. 12, n. 1, p. 154, doi. 10.1186/1471-2229-12-154
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- Article
Experimental validation of non‐Newtonian stratified co‐extrusion prediction models using a digital process twin.
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- Polymer Engineering & Science, 2022, v. 62, n. 12, p. 3902, doi. 10.1002/pen.26147
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- Article
COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.
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- Human Genetics, 2019, v. 138, n. 10, p. 1105, doi. 10.1007/s00439-019-02042-4
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- Article
Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.
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- Human Genetics, 2015, v. 134, n. 8, p. 905, doi. 10.1007/s00439-015-1570-5
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- Article
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy.
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- Human Genetics, 2013, v. 132, n. 8, p. 865, doi. 10.1007/s00439-013-1297-0
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- Article
KANK deficiency leads to podocyte dysfunction and nephrotic syndrome.
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- Journal of Clinical Investigation, 2015, v. 125, n. 6, p. 2375, doi. 10.1172/JCI79504
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A classification of the finite non-solvable minimal non-CA-groups.
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- Journal of Algebra & Its Applications, 2021, v. 20, n. 11, p. 1, doi. 10.1142/S0219498821502030
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The Collatz conjecture in a group theoretic context.
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- Journal of Group Theory, 2017, v. 20, n. 5, p. 1025, doi. 10.1515/jgth-2017-0012
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Die Burghut – Häuser der Ministerialen und Burgmannen auf Burgen der Stauferzeit.
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- Burgen und Schlösser, 2023, v. 64, n. 3, p. 145
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A simple group generated by involutions interchanging residue classes of the integers.
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- Mathematische Zeitschrift, 2010, v. 264, n. 4, p. 927, doi. 10.1007/s00209-009-0497-8
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Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
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- Pediatric Nephrology, 2014, v. 29, n. 4, p. 695, doi. 10.1007/s00467-013-2684-4
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Description of last instar larvae of Ceratogomphus triceraticus Balinsky, 1963 and C. pictus Hagen in Selys, 1854 (Odonata: Gomphidae).
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- International Journal of Odonatology, 2021, v. 24, p. 247, doi. 10.23797/2159-6719_24_19
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Simple groups generated by involutions interchanging residue classes modulo lattices in ℤ<sup> d</sup>.
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- Journal of Group Theory, 2013, v. 16, n. 1, p. 81, doi. 10.1515/jgt-2012-0031
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- Article
Increasing Sucrose Uptake Capacity of Wheat Grains Stimulates Storage Protein Synthesis.
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- Plant Physiology, 2010, v. 152, n. 2, p. 698, doi. 10.1104/pp.109.150854
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- Article
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.
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- Human Mutation, 2015, v. 36, n. 12, p. 1150, doi. 10.1002/humu.22859
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Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract.
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- Nephrology Dialysis Transplantation, 2016, v. 31, n. 8, p. 1280, doi. 10.1093/ndt/gfv447
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A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux.
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- PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0191224
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