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Deep‐Learning Based Causal Inference: A Feasibility Study Based on Three Years of Tectonic‐Climate Data From Moxa Geodynamic Observatory.
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- Earth & Space Science, 2024, v. 11, n. 10, p. 1, doi. 10.1029/2023EA003430
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- Article
Sequence variants underlying severe combined immunodeficiency and leukocyte adhesion deficiency type 1 in six consanguineous families.
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- Immunogenetics, 2024, v. 76, n. 5/6, p. 351, doi. 10.1007/s00251-024-01353-9
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- Article
Therapeutic Evaluation of Unani Medicine, Including Single Drugs and Polyherbal Formulations with Special Reference to Neurodegenerative Disorders.
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- Alternative Therapies in Health & Medicine, 2024, v. 30, n. 9, p. 54
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- Article
Evaluating the effects of as-casted and aged overcasting of Al-Al joints.
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- International Journal of Advanced Manufacturing Technology, 2018, v. 96, n. 1-4, p. 1377, doi. 10.1007/s00170-018-1682-x
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- Article
Effects of wire-Cut EDM process parameters on surface roughness of HSLA steel.
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- International Journal of Advanced Manufacturing Technology, 2017, v. 91, n. 5-8, p. 1867, doi. 10.1007/s00170-016-9881-9
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- Article
Investigating the effects of as-casted and in situ heat-treated squeeze casting of Al-3.5 % Cu alloy.
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- International Journal of Advanced Manufacturing Technology, 2017, v. 89, n. 9-12, p. 3547, doi. 10.1007/s00170-016-9350-5
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- Article
Modeling of weld bead geometry on HSLA steel using response surface methodology.
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- International Journal of Advanced Manufacturing Technology, 2017, v. 89, n. 5-8, p. 2087, doi. 10.1007/s00170-016-9213-0
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- Article
Predicting the tensile strength, impact toughness, and hardness of friction stir-welded AA6061-T6 using response surface methodology.
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- International Journal of Advanced Manufacturing Technology, 2016, v. 87, n. 5-8, p. 1765, doi. 10.1007/s00170-016-8565-9
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- Article
Parametric analysis of recast layer formation in wire-cut EDM of HSLA steel.
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- International Journal of Advanced Manufacturing Technology, 2016, v. 87, n. 1-4, p. 713, doi. 10.1007/s00170-016-8518-3
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- Article
Surface roughness modeling using RSM for HSLA steel by coated carbide tools.
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- International Journal of Advanced Manufacturing Technology, 2015, v. 78, n. 5-8, p. 1031, doi. 10.1007/s00170-014-6707-5
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- Article
An innovative cost modelling system to support lean product and process development.
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- International Journal of Advanced Manufacturing Technology, 2013, v. 65, n. 1-4, p. 165, doi. 10.1007/s00170-012-4158-4
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- Article
Preliminary Maturity Level Assessment of Industry 4.0 in the Context of Pakistani Industries.
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- Engineering Proceedings, 2023, v. 45, p. 1, doi. 10.3390/engproc2023045029
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- Article
Trichoderma-Mediated ZnO Nanoparticles and Their Antibiofilm and Antibacterial Activities.
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- Journal of Fungi, 2023, v. 9, n. 2, p. 133, doi. 10.3390/jof9020133
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- Article
A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment.
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- Human Genetics, 2018, v. 137, n. 6/7, p. 471, doi. 10.1007/s00439-018-1899-7
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- Article
Mutation of ATF6 causes autosomal recessive achromatopsia.
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- Human Genetics, 2015, v. 134, n. 9, p. 941, doi. 10.1007/s00439-015-1571-4
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- Article
Genetic mapping of an autosomal recessive postaxial polydactyly type A to chromosome 13q13.3-q21.2 and screening of the candidate genes.
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- Human Genetics, 2012, v. 131, n. 3, p. 415, doi. 10.1007/s00439-011-1085-7
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- Article
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.
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- Human Genetics, 2011, v. 130, n. 6, p. 759, doi. 10.1007/s00439-011-1018-5
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- Article
DFNB89 , a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2.
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- Human Genetics, 2011, v. 129, n. 4, p. 379, doi. 10.1007/s00439-010-0934-0
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- Article
Novel mutations in the keratin-74 ( KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families.
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- Human Genetics, 2011, v. 129, n. 4, p. 419, doi. 10.1007/s00439-010-0938-9
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- Article
Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes.
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- Human Genetics, 2010, v. 128, n. 2, p. 213, doi. 10.1007/s00439-010-0847-y
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- Article
Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3.
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- Human Genetics, 2010, v. 127, n. 4, p. 395, doi. 10.1007/s00439-009-0784-9
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- Article
Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.
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- Human Genetics, 2009, v. 125, n. 4, p. 421, doi. 10.1007/s00439-009-0640-y
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- Article
Novel mutations in G protein-coupled receptor gene ( P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
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- Human Genetics, 2008, v. 123, n. 5, p. 515, doi. 10.1007/s00439-008-0507-7
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- Article
A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22–q11.2.
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- Human Genetics, 2008, v. 123, n. 1, p. 77, doi. 10.1007/s00439-007-0452-x
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- Article
A mutation in the lipase H ( LIPH) gene underlie autosomal recessive hypotrichosis.
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- Human Genetics, 2007, v. 121, n. 3/4, p. 319, doi. 10.1007/s00439-007-0344-0
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- Article
DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.
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- Human Genetics, 2006, v. 120, n. 1, p. 85, doi. 10.1007/s00439-006-0188-z
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- Article
Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33–q27.3.
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- Human Genetics, 2006, v. 118, n. 5, p. 665, doi. 10.1007/s00439-005-0086-9
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- Article
A novel autosomal recessive non-syndromic hearing impairment locus ( DFNB47) maps to chromosome 2p25.1-p24.3.
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- Human Genetics, 2006, v. 118, n. 5, p. 605, doi. 10.1007/s00439-005-0079-8
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- Article
Self-concept among teacher trainees of B.Ed. general and special education.
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- Indian Journal of Positive Psychology, 2021, v. 12, n. 1, p. 96
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- Article
MULTI-RAT BASED ADAPTIVE QUALITY OF SERVICE (QOS) MANAGEMENT IN WBAN.
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- Malaysian Journal of Computer Science, 2020, v. 33, n. 4, p. 252, doi. 10.22452/mjcs.vol33no4.1
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- Article
FSI DRIVENERGY: MITIGATING SMARTPHONE ENERGY CONSUMPTION USING FUZZY INFERENCE.
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- Malaysian Journal of Computer Science, 2020, v. 33, n. 3, p. 188, doi. 10.22452/mjcs.vol33no3.2
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- Article
AN INVESTIGATION OF VIDEO COMMUNICATION OVER BANDWIDTH LIMITED PUBLIC SAFETY NETWORK.
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- Malaysian Journal of Computer Science, 2018, v. 31, n. 2, p. 85, doi. 10.22452/mjcs.vol31no2.1
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- Article
COUNSELING WITH PATIENTS: STILL A DILEMMA.
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- 2016
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- Letter to the Editor
Incidence of External Ear Canal Folliculitis.
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- Journal of Rawalpindi Medical College, 2017, v. 21, n. 1, p. 75
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- Article
Bayesian Markov switching model for BRICS currencies' exchange rates.
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- Journal of Forecasting, 2024, v. 43, n. 6, p. 2322, doi. 10.1002/for.3128
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- Article
Identification of kidney stones in KUB X-ray images using VGG16 empowered with explainable artificial intelligence.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-56478-4
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- Article
Polyphenols and Their Nanoformulations: Protective Effects against Human Diseases.
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- Life (2075-1729), 2022, v. 12, n. 10, p. 1639, doi. 10.3390/life12101639
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- Article
Pharmacological Efficacy of Probiotics in Respiratory Viral Infections: A Comprehensive Review.
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- Journal of Personalized Medicine, 2022, v. 12, n. 8, p. 1292, doi. 10.3390/jpm12081292
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- Article
Frameshift Sequence Variants in the Human Lipase-H Gene Causing Hypotrichosis.
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- Pediatric Dermatology, 2016, v. 33, n. 1, p. e40, doi. 10.1111/pde.12727
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- Article
A Novel Nonsense Mutation in RSPO4 Gene Underlies Autosomal Recessive Congenital Anonychia in a Pakistani Family.
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- Pediatric Dermatology, 2013, v. 30, n. 1, p. 139, doi. 10.1111/j.1525-1470.2011.01587.x
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- Article
Formulation of lemongrass oil (Cymbopogon citratus)-loaded solid lipid nanoparticles: an in vitro assessment study.
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- 3 Biotech, 2023, v. 13, n. 9, p. 1, doi. 10.1007/s13205-023-03726-5
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- Article
Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families.
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- International Journal of Dermatology, 2017, v. 56, n. 12, p. 1406, doi. 10.1111/ijd.13778
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- Article
Disease causing homozygous variants in the human hairless gene.
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- International Journal of Dermatology, 2016, v. 55, n. 9, p. 977, doi. 10.1111/ijd.13109
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- Article
Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis.
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- International Journal of Dermatology, 2016, v. 55, n. 5, p. 524, doi. 10.1111/ijd.12950
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- Article
A novel missense mutation in the ectodysplasin-A ( EDA) gene underlies X-linked recessive nonsyndromic hypodontia.
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- International Journal of Dermatology, 2010, v. 49, n. 12, p. 1399, doi. 10.1111/j.1365-4632.2010.04596.x
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- Article
Application of set‐based concurrent engineering methodology to the development of cost modeling system for metal casting process.
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- Systems Engineering, 2023, v. 26, n. 2, p. 162, doi. 10.1002/sys.21648
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- Article
Prospective Epigenetic Actions of Organo-Sulfur Compounds against Cancer: Perspectives and Molecular Mechanisms.
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- Cancers, 2023, v. 15, n. 3, p. 697, doi. 10.3390/cancers15030697
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- Article
A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families.
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- Genetics Research International, 2011, p. 1, doi. 10.4061/2011/368915
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- Article
Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene.
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- Genetics Research International, 2011, p. 1, doi. 10.4061/2011/294675
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- Article
Do new CEOs really care about innovation?
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- European Financial Management, 2024, v. 30, n. 1, p. 230, doi. 10.1111/eufm.12411
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- Article