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Oxidative stress induced necroptosis activation is involved in the pathogenesis of hyperoxic acute lung injury

Biochemical and biophysical research communications, 2018-01, Vol.495 (3), p.2178-2183

2018

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Corrigendum to “DEPDC1B enhances migration and invasion of non-small cell lung cancer cells via activating Wnt/β-catenin signaling” [Biochem. Biophys. Res. Commun. 450(1) (2014) 899–905]

Biochemical and biophysical research communications, 2021-09, Vol.568, p.195-195

2021

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DNA binding properties of 9-substituted harmine derivatives

Biochemical and biophysical research communications, 2005-12, Vol.338 (3), p.1557-1563

2005

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Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation

Biochemical and biophysical research communications, 2009-06, Vol.383 (3), p.286-292

2009

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Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation

Biochemical and biophysical research communications, 2009-11, Vol.389 (3), p.466-472

2009

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Leber’s hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families

Biochemical and biophysical research communications, 2006-02, Vol.340 (1), p.69-75

2006

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Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness

Biochemical and biophysical research communications, 2006-02, Vol.340 (1), p.194-199

2006

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Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation

Biochemical and biophysical research communications, 2005-03, Vol.328 (4), p.1244-1251

2005

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Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber’s hereditary optic neuropathy

Biochemical and biophysical research communications, 2005-07, Vol.332 (2), p.614-621

2005

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The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family

Biochemical and biophysical research communications, 2007-10, Vol.362 (3), p.670-676

2007

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Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation

Biochemical and biophysical research communications, 2006-02, Vol.340 (2), p.583-588

2006

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Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation

Biochemical and biophysical research communications, 2004-12, Vol.325 (4), p.1503-1508

2004

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The effect of the mtDNA4834 deletion on hearing

Biochemical and biophysical research communications, 2006-05, Vol.344 (1), p.425-430

2006

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Induction of MHC class I-related chain B (MICB) by 5-aza-2′-deoxycytidine

Biochemical and biophysical research communications, 2008-06, Vol.370 (4), p.578-583

2008

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Only male matrilineal relatives with Leber’s hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation

Biochemical and biophysical research communications, 2005-03, Vol.328 (4), p.1139-1145

2005

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The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber’s hereditary optic neuropathy and hearing loss

Biochemical and biophysical research communications, 2007-06, Vol.357 (4), p.910-916

2007

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β-carboline derivatives: Novel photosensitizers that intercalate into DNA to cause direct DNA damage in photodynamic therapy

Biochemical and biophysical research communications, 2006-04, Vol.342 (3), p.894-901

2006

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Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss

Biochemical and biophysical research communications, 2005-10, Vol.336 (3), p.967-973

2005

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Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNA{sup Ser(UCN)} genes in two Chinese families

Biochemical and biophysical research communications, 2006-04, Vol.342 (3)

2006

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Sodium channel-mediated intrinsic mechanisms underlying the differences of spike programming among GABAergic neurons

Biochemical and biophysical research communications, 2006-07, Vol.346 (1), p.281-287

2006

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Discoidin domain receptor 2 is involved in the activation of bone marrow-derived dendritic cells caused by type I collagen

Biochemical and biophysical research communications, 2007-01, Vol.352 (1), p.244-250

2007

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Leber’s hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families

Biochemical and biophysical research communications, 2006-08, Vol.347 (1), p.221-225

2006

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Liver-X-receptor activator prevents homocysteine-induced production of IgG antibodies from murine B lymphocytes via the ROS–NF-κB pathway

Biochemical and biophysical research communications, 2007-06, Vol.357 (3), p.772-778

2007

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The postnatal development of intrinsic properties and spike encoding at cortical GABAergic neurons

Biochemical and biophysical research communications, 2009-01, Vol.378 (4), p.706-710

2009

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Congenital long QT syndrome caused by the F275S KCNQ1 mutation: Mechanism of impaired channel function

Biochemical and biophysical research communications, 2009-02, Vol.380 (1), p.127-131

2009

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Oxidative stress induced necroptosis activation is involved in the pathogenesis of hyperoxic acute lung injury

Corrigendum to “DEPDC1B enhances migration and invasion of non-small cell lung cancer cells via activating Wnt/β-catenin signaling” [Biochem. Biophys. Res. Commun. 450(1) (2014) 899–905]

DNA binding properties of 9-substituted harmine derivatives

Leber’s hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation

Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation

Leber’s hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber’s hereditary optic neuropathy

The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family

Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation

The effect of the mtDNA4834 deletion on hearing

Induction of MHC class I-related chain B (MICB) by 5-aza-2′-deoxycytidine

Only male matrilineal relatives with Leber’s hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation

The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber’s hereditary optic neuropathy and hearing loss

β-carboline derivatives: Novel photosensitizers that intercalate into DNA to cause direct DNA damage in photodynamic therapy

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss

Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNA{sup Ser(UCN)} genes in two Chinese families

Sodium channel-mediated intrinsic mechanisms underlying the differences of spike programming among GABAergic neurons

Discoidin domain receptor 2 is involved in the activation of bone marrow-derived dendritic cells caused by type I collagen

Leber’s hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families

Liver-X-receptor activator prevents homocysteine-induced production of IgG antibodies from murine B lymphocytes via the ROS–NF-κB pathway

The postnatal development of intrinsic properties and spike encoding at cortical GABAergic neurons

Congenital long QT syndrome caused by the F275S KCNQ1 mutation: Mechanism of impaired channel function

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