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Search Results - Nöthe-Menchen, T
Search Results - Nöthe-Menchen, T
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Pathogenic gene variants in CCDC39 , CCDC40 , RSPH1 , RSPH9 , HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility
by
Aprea, I
,
Wilken, A
,
Krallmann, C
,
Nöthe-Menchen, T
,
Olbrich, H
,
Loges, N T
,
Dougherty, G W
,
Bracht, D
,
Brenker, C
,
Kliesch, S
,
Strünker, T
,
Tüttelmann, F
,
Raidt, J
,
Omran, H
Published in
Frontiers in genetics
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Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility
by
Aprea, Isabella
,
Raidt, Johanna
,
Höben, Inga Marlena
,
Loges, Niki Tomas
,
Nöthe-Menchen, Tabea
,
Pennekamp, Petra
,
Olbrich, Heike
,
Kaiser, Thomas
,
Biebach, Luisa
,
Tüttelmann, Frank
,
Horvath, Judit
,
Schubert, Maria
,
Krallmann, Claudia
,
Kliesch, Sabine
,
Omran, Heymut
Published in
PLoS genetics
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Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system
by
Aprea, Isabella
,
Nöthe-Menchen, Tabea
,
Dougherty, Gerard W
,
Raidt, Johanna
,
Loges, Niki T
,
Kaiser, Thomas
,
Wallmeier, Julia
,
Olbrich, Heike
,
Strünker, Timo
,
Kliesch, Sabine
,
Pennekamp, Petra
,
Omran, Heymut
Published in
Molecular human reproduction
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Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects
by
Loges, Niki T.
,
Antony, Dinu
,
Maver, Ales
,
Deardorff, Matthew A.
,
Güleç, Elif Yýlmaz
,
Gezdirici, Alper
,
Nöthe-Menchen, Tabea
,
Höben, Inga M.
,
Jelten, Lena
,
Frank, Diana
,
Werner, Claudius
,
Tebbe, Johannes
,
Wu, Kaman
,
Goldmuntz, Elizabeth
,
Čuturilo, Goran
,
Krock, Bryan
,
Ritter, Alyssa
,
Hjeij, Rim
,
Bakey, Zeineb
,
Pennekamp, Petra
,
Dworniczak, Bernd
,
Brunner, Han
,
Peterlin, Borut
,
Tanidir, Cansaran
,
Olbrich, Heike
,
Omran, Heymut
,
Schmidts, Miriam
Published in
American journal of human genetics
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CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module
by
Dougherty, Gerard W.
,
Mizuno, Katsutoshi
,
Nöthe-Menchen, Tabea
,
Ikawa, Yayoi
,
Boldt, Karsten
,
Ta-Shma, Asaf
,
Aprea, Isabella
,
Minegishi, Katsura
,
Pang, Yuan-Ping
,
Pennekamp, Petra
,
Loges, Niki T.
,
Raidt, Johanna
,
Hjeij, Rim
,
Wallmeier, Julia
,
Mussaffi, Huda
,
Perles, Zeev
,
Elpeleg, Orly
,
Rabert, Franziska
,
Shiratori, Hidetaka
,
Letteboer, Stef J.
,
Horn, Nicola
,
Young, Samuel
,
Strünker, Timo
,
Stumme, Friederike
,
Werner, Claudius
,
Olbrich, Heike
,
Takaoka, Katsuyoshi
,
Ide, Takahiro
,
Twan, Wang Kyaw
,
Biebach, Luisa
,
Große-Onnebrink, Jörg
,
Klinkenbusch, Judith A.
,
Praveen, Kavita
,
Bracht, Diana C.
,
Höben, Inga M.
,
Junger, Katrin
,
Gützlaff, Jana
,
Cindrić, Sandra
,
Aviram, Micha
,
Kaiser, Thomas
,
Memari, Yasin
,
Dzeja, Petras P.
,
Dworniczak, Bernd
,
Ueffing, Marius
,
Roepman, Ronald
,
Bartscherer, Kerstin
,
Katsanis, Nicholas
,
Davis, Erica E.
,
Amirav, Israel
,
Hamada, Hiroshi
,
Omran, Heymut
Published in
Nature communications
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Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility
by
Ta-Shma, Asaf
,
Hjeij, Rim
,
Perles, Zeev
,
Dougherty, Gerard W
,
Abu Zahira, Ibrahim
,
Letteboer, Stef J F
,
Antony, Dinu
,
Darwish, Alaa
,
Mans, Dorus A
,
Spittler, Sabrina
,
Edelbusch, Christine
,
Cindrić, Sandra
,
Nöthe-Menchen, Tabea
,
Olbrich, Heike
,
Stuhlmann, Friederike
,
Aprea, Isabella
,
Pennekamp, Petra
,
Loges, Niki T
,
Breuer, Oded
,
Shaag, Avraham
,
Rein, Azaria J J T
,
Gulec, Elif Yilmaz
,
Gezdirici, Alper
,
Abitbul, Revital
,
Elias, Nael
,
Amirav, Israel
,
Schmidts, Miriam
,
Roepman, Ronald
,
Elpeleg, Orly
,
Omran, Heymut
Published in
PLoS genetics
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miR449 Protects Airway Regeneration by Controlling AURKA/HDAC6-Mediated Ciliary Disassembly
by
Wildung, Merit
,
Herr, Christian
,
Riedel, Dietmar
,
Wiedwald, Cornelia
,
Moiseenko, Alena
,
Ramírez, Fidel
,
Tasena, Hataitip
,
Heimerl, Maren
,
Alevra, Mihai
,
Movsisyan, Naira
,
Schuldt, Maike
,
Volceanov-Hahn, Larisa
,
Provoost, Sharen
,
Nöthe-Menchen, Tabea
,
Urrego, Diana
,
Freytag, Bernard
,
Wallmeier, Julia
,
Beisswenger, Christoph
,
Bals, Robert
,
van den Berge, Maarten
,
Timens, Wim
,
Hiemstra, Pieter S.
,
Brandsma, Corry-Anke
,
Maes, Tania
,
Andreas, Stefan
,
Heijink, Irene H.
,
Pardo, Luis A.
,
Lizé, Muriel
Published in
International journal of molecular sciences
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De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry
by
Wallmeier, Julia
,
Frank, Diana
,
Shoemark, Amelia
,
Nöthe-Menchen, Tabea
,
Cindric, Sandra
,
Olbrich, Heike
,
Loges, Niki T.
,
Aprea, Isabella
,
Dougherty, Gerard W.
,
Pennekamp, Petra
,
Kaiser, Thomas
,
Mitchison, Hannah M.
,
Hogg, Claire
,
Carr, Siobhán B.
,
Zariwala, Maimoona A.
,
Ferkol, Thomas
,
Leigh, Margaret W.
,
Davis, Stephanie D.
,
Atkinson, Jeffrey
,
Dutcher, Susan K.
,
Knowles, Michael R.
,
Thiele, Holger
,
Altmüller, Janine
,
Krenz, Henrike
,
Wöste, Marius
,
Brentrup, Angela
,
Ahrens, Frank
,
Vogelberg, Christian
,
Morris-Rosendahl, Deborah J.
,
Omran, Heymut
Published in
American journal of human genetics
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Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms
by
Höben, Inga M.
,
Hjeij, Rim
,
Olbrich, Heike
,
Dougherty, Gerard W.
,
Nöthe-Menchen, Tabea
,
Aprea, Isabella
,
Frank, Diana
,
Pennekamp, Petra
,
Dworniczak, Bernd
,
Wallmeier, Julia
,
Raidt, Johanna
,
Nielsen, Kim G.
,
Philipsen, Maria C.
,
Santamaria, Francesca
,
Venditto, Laura
,
Amirav, Israel
,
Mussaffi, Huda
,
Prenzel, Freerk
,
Wu, Kaman
,
Bakey, Zeineb
,
Schmidts, Miriam
,
Loges, Niki T.
,
Omran, Heymut
Published in
American journal of human genetics
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