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Influence of graphite edge crystallographic orientation on the first lithium intercalation in Li-ion battery

Carbon (New York), 2015-09, Vol.91, p.458-467

2015

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Large structure response to high frequency excitation from rock blasting

International journal of rock mechanics and mining sciences (Oxford, England : 1997), 2018-11, Vol.111, p.54-63

2018

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Synthesis of polymer nanocomposites by UV-curing of organoclay–acrylic resins

Polymer (Guilford), 2004-10, Vol.45 (22), p.7437-7447

2004

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Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

Journal of medical genetics, 2005-02, Vol.42 (2), p.e12-e12

2005

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MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

American journal of human genetics, 2001-05, Vol.68 (5), p.1093-1101

2001

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Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome

Journal of medical genetics, 2010-01, Vol.47 (1), p.30-37

2010

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Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1 similar to 27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin

Cytogenetic and genome research, 2012-04, Vol.136 (3), p.163-166

2012

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Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin

Cytogenetic and genome research, 2012-04, Vol.136 (3), p.163-166

2012

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Phase Transitions in the Na3M2(PO4)2F3 Family (M=Al3+, V3+, Cr3+, Fe3+, Ga3+): Synthesis, Thermal, Structural, and Magnetic Studies

Journal of solid state chemistry, 1999-12, Vol.148 (2), p.260-277

1999

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Coupling socio-economic factors and eco-hydrological processes using a cascade-modeling approach

Journal of hydrology (Amsterdam), 2014-10, Vol.518, p.49-59

2014

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Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regions

Human mutation, 2001-03, Vol.17 (3), p.183-190

2001

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Characterisation of hydroclimatological trends and variability in the Lake Naivasha basin, Kenya

Hydrological processes, 2015-07, Vol.29 (15), p.3276-3293

2015

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10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

Cytogenetic and genome research, 2009-04, Vol.124 (1), p.102-105

2009

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The Effects of Groundwater and Surface Water Use on Total Water Availability and Implications for Water Management: The Case of Lake Naivasha, Kenya

Water resources management, 2013-07, Vol.27 (9), p.3477-3492

2013

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Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome

Journal of medical genetics, 2003-05, Vol.40 (5), p.e62-62

2003

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Variable and multiple expression of Protease Nexin-1 during mouse organogenesis and nervous system development

Development (Cambridge), 1993-12, Vol.119 (4), p.1119-1134

1993

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Ionic conductivity of crystalline and amorphous Na3Al2(PO4)2F3

Solid state ionics, 1998-08, Vol.111 (1-2), p.67-75

1998

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Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients

Neuropediatrics, 2002-08, Vol.33 (4), p.194

2002

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Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease

Neuropediatrics, 2007-06, Vol.38 (3), p.143

2007

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Cysteine phosphorylation of the glucose transporter of Escherichia coli

The Journal of biological chemistry, 1993-06, Vol.268 (16), p.11604-11609

1993

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A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis

Cytogenetic and genome research, 2002-01, Vol.98 (1), p.1-8

2002

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First non‐mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter → q22.1::q22.1 → pter) Is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q− syndrome

American journal of medical genetics, 2004-05, Vol.127A (1), p.58-64

2004

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Identification and characterization of murine Brunol4, a new member of the elav/bruno family

Cytogenetic and genome research, 2002, Vol.97 (3-4), p.254-260

2002

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Thrombin in ischemic neuronal death

Experimental neurology, 2006-03, Vol.198 (1), p.199-203

2006

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SrFeP2O7, a new homologue in the AMP2O7 series

Acta crystallographica. Section C, Crystal structure communications, 1999-04, Vol.55 (4), p.481-483

1999

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Influence of graphite edge crystallographic orientation on the first lithium intercalation in Li-ion battery

Large structure response to high frequency excitation from rock blasting

Synthesis of polymer nanocomposites by UV-curing of organoclay–acrylic resins

Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome

Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1 similar to 27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin

Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin

Phase Transitions in the Na3M2(PO4)2F3 Family (M=Al3+, V3+, Cr3+, Fe3+, Ga3+): Synthesis, Thermal, Structural, and Magnetic Studies

Coupling socio-economic factors and eco-hydrological processes using a cascade-modeling approach

Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regions

Characterisation of hydroclimatological trends and variability in the Lake Naivasha basin, Kenya

10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences

The Effects of Groundwater and Surface Water Use on Total Water Availability and Implications for Water Management: The Case of Lake Naivasha, Kenya

Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome

Variable and multiple expression of Protease Nexin-1 during mouse organogenesis and nervous system development

Ionic conductivity of crystalline and amorphous Na3Al2(PO4)2F3

Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients

Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander disease

Cysteine phosphorylation of the glucose transporter of Escherichia coli

A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis

First non‐mosaic case of isopseudodicentric chromosome 18 (psu idic(18)(pter → q22.1::q22.1 → pter) Is associated with multiple congenital anomalies reminiscent of trisomy 18 and 18q− syndrome

Identification and characterization of murine Brunol4, a new member of the elav/bruno family

Thrombin in ischemic neuronal death

SrFeP2O7, a new homologue in the AMP2O7 series

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