(Q28209818)

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

21 March 2024

author name string

Nobutaka Hirokawa

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Reiko Takemura

full work available at URL

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language of work or name

English

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publication date

October 2003

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https://api.elsevier.com/content/article/PII:S0968000403002159?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

https://api.elsevier.com/content/article/PII:S0968000403002159?httpAccept=text/plain

21 March 2024

1 reference

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Trends in Biochemical Sciences

21 March 2024

published in

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volume

28

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issue

10

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page(s)

558-65

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cites work

Kinesin and dynein superfamily proteins and the mechanism of organelle transport

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

All kinesin superfamily protein, KIF, genes in mouse and human

21 March 2024

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

21 March 2024

Intraflagellar transport

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

21 March 2024

5

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Axonal transport of amyloid precursor protein is mediated by direct binding to the kinesin light chain subunit of kinesin-I

21 March 2024

6

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Kinesin-mediated axonal transport of a membrane compartment containing beta-secretase and presenilin-1 requires APP

21 March 2024

7

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

21 March 2024

8

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Stirring up development with the heterotrimeric kinesin KIF3.

21 March 2024

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Genetics and pathogenesis of polycystic kidney disease.

21 March 2024

10

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice.

21 March 2024

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia

21 March 2024

12

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium

21 March 2024

13

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella

21 March 2024

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

21 March 2024

15

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Left-right asymmetry and kinesin superfamily protein KIF3A: new insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis

21 March 2024

16

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Genetic evidence for selective transport of opsin and arrestin by kinesin-II in mammalian photoreceptors

21 March 2024

17

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

21 March 2024

21

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)

21 March 2024

22

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia

21 March 2024

23

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus

21 March 2024

24

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

21 March 2024

25

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesia

21 March 2024

26

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

LIS1: cellular function of a disease-causing gene

21 March 2024

27

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

LIS1 and dynein motor function in neuronal migration and development

21 March 2024

28

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

21 March 2024

29

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).

21 March 2024

30

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1

21 March 2024

31

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Role of dynein, dynactin, and CLIP-170 interactions in LIS1 kinetochore function

21 March 2024

32

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

A millennial myosin census

21 March 2024

33

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

The Genetic Basis for Cardiomyopathy

21 March 2024

35

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Decoding calcium signals involved in cardiac growth and function

21 March 2024

36

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.

21 March 2024

37

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

21 March 2024

38

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Usher syndrome: from genetics to pathogenesis.

21 March 2024

39

1 reference

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Molecular genetics of hearing loss

21 March 2024

40

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

A type VII myosin encoded by the mouse deafness gene shaker-1

21 March 2024

41

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 March 2024

42

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene

21 March 2024

43

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

21 March 2024

44

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Cell adhesion: ushering in a new understanding of myosin VII.

21 March 2024

45

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B

21 March 2024

46

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

21 March 2024

48

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

21 March 2024

49

1 reference

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Hair cells in the inner ear of the pirouette and shaker 2 mutant mice

21 March 2024

50

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

21 March 2024

51

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

21 March 2024

52

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

21 March 2024

53

1 reference

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

The melanosome: membrane dynamics in black and white

21 March 2024

54

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Rab GTPases, intracellular traffic and disease.

21 March 2024

55

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

21 March 2024

56

1 reference

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

A mutation in Rab27a causes the vesicle transport defects observed in ashen mice

21 March 2024

57

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Rab27a: A key to melanosome transport in human melanocytes

21 March 2024

58

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Rab27a is an essential component of melanosome receptor for myosin Va

21 March 2024

59

1 reference

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Novel myosin heavy chain encoded by murine dilute coat colour locus

21 March 2024

60

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene

21 March 2024

61

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Melanophilin, the product of the leaden locus, is required for targeting of myosin-Va to melanosomes

21 March 2024

62

1 reference

https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Defective granule exocytosis in Rab27a-deficient lymphocytes from Ashen mice

21 March 2024

63

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

Rab27a is required for regulated secretion in cytotoxic T lymphocytes

21 March 2024

64

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https://api.crossref.org/works/10.1016/J.TIBS.2003.08.006

21 March 2024

Identifiers