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Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility.
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- Reproductive Sciences, 2022, v. 29, n. 9, p. 2697, doi. 10.1007/s43032-022-00965-4
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- Article
Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain.
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- Human Genetics, 2020, v. 139, n. 4, p. 545, doi. 10.1007/s00439-020-02123-9
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- Article
Investigation on the Mechanism of PAL (100) Surface Modified by APTES.
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- Molecules, 2023, v. 28, n. 14, p. 5417, doi. 10.3390/molecules28145417
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- Article
Transmit/Receive Spatial Smoothing with Improved Effective Array Aperture for Angle and Mutual Coupling Estimation in Bistatic MIMO Radar.
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- International Journal of Antennas & Propagation, 2016, p. 1, doi. 10.1155/2016/6271648
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- Article
Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.
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- Reproductive Sciences, 2022, v. 29, n. 10, p. 3047, doi. 10.1007/s43032-022-00958-3
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- Article
A novel homozygous mutation in ACTL7A leads to male infertility.
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- Molecular Genetics & Genomics, 2023, v. 298, n. 2, p. 353, doi. 10.1007/s00438-022-01985-0
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- Article
Tsga10 is essential for arrangement of mitochondrial sheath and male fertility in mice.
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- Andrology, 2021, v. 9, n. 1, p. 368, doi. 10.1111/andr.12889
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Three novel compound heterozygous IL12RB1 mutations in Chinese patients with Mendelian susceptibility to mycobacterial disease.
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- PLoS ONE, 2019, v. 14, n. 4, p. 1, doi. 10.1371/journal.pone.0215648
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- Article
Novel mutations in ZP2 and ZP3 cause female infertility in three patients.
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- Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 5, p. 1205, doi. 10.1007/s10815-022-02466-4
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- Article
A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation.
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- Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 1, p. 251, doi. 10.1007/s10815-020-01995-0
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- Article
A novel UBE2A mutation in a Chinese family with X‐linked intellectual disability.
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- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3191
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- Article
A novel mutation in the GALC gene causes Krabbe disease accompanied with extensive Mongolian spots in a consanguineous family.
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- Neurological Sciences, 2023, v. 44, n. 7, p. 2605, doi. 10.1007/s10072-023-06748-2
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- Article
Null Broadening Robust Beamforming Based on Decomposition and Iterative Second-order Cone Programming.
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- Radioengineering, 2021, v. 30, n. 4, p. 680, doi. 10.13164/re.2021.0680
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- Article
Robust Adaptive Beamforming using k-means Clustering: A Solution to High Complexity of the Reconstruction-Based Algorithm.
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- Radioengineering, 2018, v. 27, n. 2, p. 595, doi. 10.13164/re.2018.0595
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- Article
Robust Tensor Analysis with Non-Greedy ℓ<sub>1</sub>-Norm Maximization.
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- Radioengineering, 2016, v. 25, n. 1, p. 200, doi. 10.13164/re.2016.0200
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- Article
Unambiguous Tracking Method Based on Combined Correlation Functions for sine/cosine-BOC CBOC and AltBOC Modulated Signals.
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- Radioengineering, 2014, v. 23, n. 1, p. 244
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- Article
SPSA-Based Tracking Method for Single-Channel-Receiver Array.
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- Radioengineering, 2013, v. 22, n. 2, p. 564
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- Article
Simultaneous Perturbation Stochastic Approximation for Unambiguous Acquisition in Cosine-BOC Signals.
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- Radioengineering, 2013, v. 22, n. 2, p. 578
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- Article
Linear-Combined-Code-Based Unambiguous Code Discriminator Design for Multipath Mitigation in GNSS Receivers.
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- Radioengineering, 2012, v. 21, n. 4, p. 1140
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- Article
Cross-Correlation-Function-Based Multipath Mitigation Method for Sine-BOC Signals.
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- Radioengineering, 2012, v. 21, n. 2, p. 659
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- Article
A User Parameter-Free Robust Adaptive Beamformer Based on General Linear Combination in Tandem with Steering Vector Estimation.
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- Wireless Personal Communications, 2014, v. 75, n. 2, p. 1447, doi. 10.1007/s11277-013-1432-1
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- Article
Complex Step-Shape Binary Offset Carrier Modulation for a Unitary Analytical Framework of GNSS Signals.
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- Wireless Personal Communications, 2013, v. 72, n. 4, p. 1915, doi. 10.1007/s11277-013-1113-0
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- Article
Complex Step-Shape Binary Offset Carrier Modulation for a Unitary Analytical Framework of GNSS Signals.
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- Wireless Personal Communications, 2013, v. 72, n. 4, p. 1915, doi. 10.1007/s11277-013-1113-0
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- Article
Estimation of the Communication Link Status in Satcom on-the-Move.
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- Wireless Personal Communications, 2013, v. 71, n. 2, p. 1297, doi. 10.1007/s11277-012-0875-0
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- Article
An Unambiguous Tracking Method Based on Pseudo Correlation Function for AltBOC(15,10) Signal.
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- Wireless Personal Communications, 2013, v. 69, n. 4, p. 1347, doi. 10.1007/s11277-012-0637-z
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- Article
Adaptable integrated sensing and communication for UAV‐empowered 6G networks.
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- Electronics Letters (Wiley-Blackwell), 2024, v. 60, n. 5, p. 1, doi. 10.1049/ell2.13117
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- Article
Joint state estimation with integrated sensing and communications for UAV enabled 6G systems.
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- Electronics Letters (Wiley-Blackwell), 2023, v. 59, n. 2, p. 1, doi. 10.1049/ell2.12722
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- Article
Dynamic deployment of multi‐UAV base stations with deep reinforcement learning.
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- Electronics Letters (Wiley-Blackwell), 2021, v. 57, n. 15, p. 600, doi. 10.1049/ell2.12205
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- Article
Efficient channel tracking strategy for mmWave UAV communications.
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- Electronics Letters (Wiley-Blackwell), 2018, v. 54, n. 21, p. 1218, doi. 10.1049/el.2018.6159
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- Article
Efficient channel tracking strategy for mmWave UAV communications.
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- Electronics Letters (Wiley-Blackwell), 2018, v. 54, n. 21, p. 1218, doi. 10.1049/el.2018.6159
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- Article
Channel transmission strategy for mmWave hybrid UAV communications with blockage.
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- Electronics Letters (Wiley-Blackwell), 2018, v. 54, n. 2, p. 74, doi. 10.1049/el.2017.4058
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- Article
Channel transmission strategy for mmWave hybrid UAV communications with blockage.
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- Electronics Letters (Wiley-Blackwell), 2018, v. 54, n. 2, p. 74, doi. 10.1049/el.2017.4058
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- Article
Attitude Estimation Based on the Spherical Simplex Transformation Modified Unscented Kalman Filter.
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- Mathematical Problems in Engineering, 2014, p. 1, doi. 10.1155/2014/925914
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- Article
A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly.
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- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 1, p. 31, doi. 10.1002/ajmg.a.62480
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- Article
Juvenile-Onset Kufs Disease in a Chinese Consanguineous Family due to CLN6 Mutation.
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- Neurodegenerative Diseases, 2022, v. 21, n. 5/6, p. 126, doi. 10.1159/000524784
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- Article