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The role of NLRP6 in the development and progression of neurological diseases
The role of NLRP6 in the development and progression of neurological diseases
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The role of NLRP6 in the development and progression of neurological diseases

Guo, Yiming ; Song, Jiaqi ; Yan, Mengyu ; Chen, Yingxi ; Huang, Lihong ; Liu, Jiarui ; He, Yurou ; Lü, Yang ; Yu, Weihua

Molecular biology reports, 2024-12, Vol.51 (1), p.351-351, Article 351 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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2
Functional implications of NHR-210 enrichment in C. elegans cephalic sheath glia: insights into metabolic and mitochondrial disruptions in Parkinson's disease models
Functional implications of NHR-210 enrichment in C. elegans cephalic sheath glia: insights into metabolic and mitochondrial disruptions in Parkinson's disease models
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Functional implications of NHR-210 enrichment in C. elegans cephalic sheath glia: insights into metabolic and mitochondrial disruptions in Parkinson's disease models

Hameed, Rohil ; Naseer, Anam ; Saxena, Ankit ; Akbar, Mahmood ; Toppo, Pranoy ; Sarkar, Arunabh ; Shukla, Sanjeev K. ; Nazir, Aamir

Cellular and molecular life sciences : CMLS, 2024-12, Vol.81 (1), p.202-202, Article 202 [Periódico revisado por pares]

Cham: Springer International Publishing

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Targeting phosphodiesterase 4 as a potential therapy for Parkinson’s disease: a review
Targeting phosphodiesterase 4 as a potential therapy for Parkinson’s disease: a review
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Targeting phosphodiesterase 4 as a potential therapy for Parkinson’s disease: a review

Nongthombam, Pooja Devi ; Haobam, Reena

Molecular biology reports, 2024-12, Vol.51 (1), p.510-510, Article 510 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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4
Impacts of β-1, 3-N-acetylglucosaminyltransferases (B3GNTs) in human diseases
Impacts of β-1, 3-N-acetylglucosaminyltransferases (B3GNTs) in human diseases
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Impacts of β-1, 3-N-acetylglucosaminyltransferases (B3GNTs) in human diseases

Xie, Anna ; Wang, Jingjing ; Liu, Yi ; Li, Guoqing ; Yang, Nanyang

Molecular biology reports, 2024-12, Vol.51 (1), p.476-476, Article 476 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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5
A compound heterozygous mutation of ERCC8 is responsible for a family with Cockayne syndrome
A compound heterozygous mutation of ERCC8 is responsible for a family with Cockayne syndrome
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A compound heterozygous mutation of ERCC8 is responsible for a family with Cockayne syndrome

Liu, Meng-Wei ; Hu, Cheng-Feng ; Jin, Jie-Yuan ; Xiang, Rong ; Fan, Liang-liang ; Li, Ya-Li ; Zhu, Lei

Molecular biology reports, 2024-12, Vol.51 (1), p.371-371, Article 371 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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6
Neuroprotection by tetramethylpyrazine and its synthesized analogues for central nervous system diseases: a review
Neuroprotection by tetramethylpyrazine and its synthesized analogues for central nervous system diseases: a review
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Neuroprotection by tetramethylpyrazine and its synthesized analogues for central nervous system diseases: a review

Feng, Fan ; Xu, Ding-Qiao ; Yue, Shi-Jun ; Chen, Yan-Yan ; Tang, Yu-Ping

Molecular biology reports, 2024-12, Vol.51 (1), p.159-159, Article 159 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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7
Unlocking the potential of adeno-associated virus in neuroscience: a brief review
Unlocking the potential of adeno-associated virus in neuroscience: a brief review
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Unlocking the potential of adeno-associated virus in neuroscience: a brief review

Minetti, Antea

Molecular biology reports, 2024-12, Vol.51 (1), p.563-563, Article 563 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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8
Exome sequencing in four families with neurodevelopmental disorders: genotype–phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN
Exome sequencing in four families with neurodevelopmental disorders: genotype–phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN
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Exome sequencing in four families with neurodevelopmental disorders: genotype–phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN

Afridi, Tehseen Ullah Khan ; Fatima, Ambrin ; Satti, Humayoon Shafique ; Akram, Zaineb ; Yousafzai, Imran Khan ; Naeem, Wajahat Bin ; Fatima, Nasreen ; Ali, Asmat ; Iqbal, Zafar ; Khan, Ayaz ; Shahzad, Muhammad ; Liu, Chunyu ; Toft, Mathias ; Zhang, Feng ; Tariq, Muhammad ; Davis, Erica E. ; Khan, Tahir N.

Molecular genetics and genomics : MGG, 2024-12, Vol.299 (1), p.55-55, Article 55 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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9
Roles of Macrophages and Their Interactions with Schwann Cells After Peripheral Nerve Injury
Roles of Macrophages and Their Interactions with Schwann Cells After Peripheral Nerve Injury
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Roles of Macrophages and Their Interactions with Schwann Cells After Peripheral Nerve Injury

Wu, Guanggeng ; Wen, Xiaoyue ; Kuang, Rui ; Lui, KoonHei Winson ; He, Bo ; Li, Ge ; Zhu, Zhaowei

Cellular and molecular neurobiology, 2024-12, Vol.44 (1), p.11-11, Article 11 [Periódico revisado por pares]

New York: Springer US

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10
Glial cell alterations in diabetes-induced neurodegeneration
Glial cell alterations in diabetes-induced neurodegeneration
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Glial cell alterations in diabetes-induced neurodegeneration

Llorián-Salvador, María ; Cabeza-Fernández, Sonia ; Gomez-Sanchez, Jose A. ; de la Fuente, Alerie G.

Cellular and molecular life sciences : CMLS, 2024-12, Vol.81 (1), p.47-47, Article 47 [Periódico revisado por pares]

Cham: Springer International Publishing

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Deste Autor:

  1. Snell, R
  2. Pettersson, H
  3. Osborn, A
  4. Field, D
  5. Bradley, W

Neste Assunto:

  1. Nervous System
  2. Nervous System
  3. Humans
  4. Science & Technology
  5. Life Sciences & Biomedicine

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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