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Why does a high-fat diet induce preeclampsia-like symptoms in pregnant rats

Neural regeneration research, 2013-07, Vol.8 (20), p.1872-1880

2013

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Effect of High- vs Low-Dose Tranexamic Acid Infusion on Need for Red Blood Cell Transfusion and Adverse Events in Patients Undergoing Cardiac Surgery: The OPTIMAL Randomized Clinical Trial

JAMA : the journal of the American Medical Association, 2022-07, Vol.328 (4), p.336

2022

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Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations

Journal of medical genetics, 2019-11, Vol.56 (11), p.750-757

2019

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Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans

Genetics in medicine, 2019-05, Vol.21 (5), p.1209-1217

2019

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RNA splicing analysis contributes to reclassifying variants of uncertain significance and improves the diagnosis of monogenic disorders

Journal of medical genetics, 2022-10, Vol.59 (10), p.1010-1016

2022

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A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans

Asian journal of andrology, 2021-03, Vol.23 (2), p.197-204

2021

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Efficacy and safety of olmesartan medoxomil‐amlodipine besylate tablet in Chinese patients with essential hypertension: A prospective, single‐arm, multi‐center, real‐world study

The journal of clinical hypertension (Greenwich, Conn.), 2024-01, Vol.26 (1), p.5-16

2024

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Multidisciplinary assessment of PFO with substantial right‐to‐left shunting and medium‐term follow‐up after PFO device closure: A single‐center experience

Journal of interventional cardiology, 2017-08, Vol.30 (4), p.362-367

2017

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A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome

Asian journal of andrology, 2018-05, Vol.20 (3), p.308-310

2018

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P869: UPDATED RESULTS OF A PHASE I, OPEN‐LABEL STUDY OF BCMA/CD19 DUAL‐TARGETING FASTCAR‐T GC012F FOR PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA (RRMM)

HemaSphere, 2023-08, Vol.7 (S3), p.e84060bf-n/a

2023

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Two new 3D Supramolecular Frameworks as Photocatalysts for Degradation of Methyl Blue

Journal of fluorescence, 2024, Vol.34 (1), p.265-273

2024

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Feasibility of Device Closure for Multiple Atrial Septal Defects With an Inferior Sinus Venosus Defect: Procedural Planning Using Three-Dimensional Printed Models

Heart, lung & circulation, 2020-06, Vol.29 (6), p.914-920

2020

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ZP2 pathogenic variants cause in vitro fertilization failure and female infertility

Genetics in medicine, 2019-02, Vol.21 (2), p.431-440

2019

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Mechanism of dihydroartemisinin-induced apoptosis in prostate cancer PC3 cells: An iTRAQ-based proteomic analysis

Life sciences (1973), 2016-07, Vol.157, p.1-11

2016

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Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development

Human molecular genetics, 2021-12, Vol.31 (2), p.219-231

2021

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Downregulation of microRNA-512-3p enhances the viability and suppresses the apoptosis of vascular endothelial cells, alleviates autophagy and endoplasmic reticulum stress as well as represses atherosclerotic lesions in atherosclerosis by adjusting spliced/unspliced ratio of X-box binding protein 1 (XBP-1S/XBP-1U)

Bioengineered, 2021-12, Vol.12 (2), p.12469-12481

2021

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Non-coding RNAs: Emerging roles in the characterization of immune microenvironment and immunotherapy of prostate cancer

Biochemical pharmacology, 2023-08, Vol.214, p.115669-115669, Article 115669

2023

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CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis

Human molecular genetics, 2021-11, Vol.30 (23), p.2240-2254

2021

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ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report

Human reproduction (Oxford), 2019-11, Vol.34 (11), p.2201-2207

2019

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DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing

Journal of medical genetics, 2018-03, Vol.55 (3), p.198-204

2018

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Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia

Human reproduction (Oxford), 2023-07, Vol.38 (7), p.1399-1411

2023

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A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination

Human reproduction (Oxford), 2024-04, Vol.39 (4), p.849-855

2024

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Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia

Journal of medical genetics, 2023-02, Vol.60 (2), p.144-153

2023

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Updated results of a phase I, open-label study of BCMA/CD19 dual-targeting fast CAR-T GC012F for patients with relapsed/refractory multiple myeloma (RRMM)

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.8005-8005

2023

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Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia

Molecular human reproduction, 2024-02, Vol.30 (2)

2024

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Why does a high-fat diet induce preeclampsia-like symptoms in pregnant rats

Effect of High- vs Low-Dose Tranexamic Acid Infusion on Need for Red Blood Cell Transfusion and Adverse Events in Patients Undergoing Cardiac Surgery: The OPTIMAL Randomized Clinical Trial

Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations

Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans

RNA splicing analysis contributes to reclassifying variants of uncertain significance and improves the diagnosis of monogenic disorders

A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans

Efficacy and safety of olmesartan medoxomil‐amlodipine besylate tablet in Chinese patients with essential hypertension: A prospective, single‐arm, multi‐center, real‐world study

Multidisciplinary assessment of PFO with substantial right‐to‐left shunting and medium‐term follow‐up after PFO device closure: A single‐center experience

A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome

P869: UPDATED RESULTS OF A PHASE I, OPEN‐LABEL STUDY OF BCMA/CD19 DUAL‐TARGETING FASTCAR‐T GC012F FOR PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA (RRMM)

Two new 3D Supramolecular Frameworks as Photocatalysts for Degradation of Methyl Blue

Feasibility of Device Closure for Multiple Atrial Septal Defects With an Inferior Sinus Venosus Defect: Procedural Planning Using Three-Dimensional Printed Models

ZP2 pathogenic variants cause in vitro fertilization failure and female infertility

Mechanism of dihydroartemisinin-induced apoptosis in prostate cancer PC3 cells: An iTRAQ-based proteomic analysis

Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development

Non-coding RNAs: Emerging roles in the characterization of immune microenvironment and immunotherapy of prostate cancer

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis

ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report

DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing

Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia

A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia

Updated results of a phase I, open-label study of BCMA/CD19 dual-targeting fast CAR-T GC012F for patients with relapsed/refractory multiple myeloma (RRMM)

Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermia

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